-
1
-
-
0025307919
-
Pregnancies from biopsied human preimplantation embryos sexed by y-specific dna amplification
-
Handyside AH, Kontogianni EH, Hardy K, Winston RM. Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification. Nature 1990; 344:768-770.
-
(1990)
Nature
, vol.344
, pp. 768-770
-
-
Handyside, A.H.1
Kontogianni, E.H.2
Hardy, K.3
Winston, R.M.4
-
2
-
-
0025132537
-
Analysis of the first polar body: Preconception genetic diagnosis
-
Verlinsky Y, Ginsberg N, Lifchez A, Valle J, Moise J, Strom CM. Analysis of the first polar body: preconception genetic diagnosis. Hum Reprod 1990; 5:826-829.
-
(1990)
Hum Reprod
, vol.5
, pp. 826-829
-
-
Verlinsky, Y.1
Ginsberg, N.2
Lifchez, A.3
Valle, J.4
Moise, J.5
Strom, C.M.6
-
3
-
-
0029941779
-
Birth of healthy children after preimplantation diagnosis of common aneuploidies by polar body fluorescent in situ hybridization analysis. Preimplantation genetic group
-
Verlinsky Y, Cieslak J, Ivakhnenko V, Lifchez A, Strom C, Kuliev A. Birth of healthy children after preimplantation diagnosis of common aneuploidies by polar body fluorescent in situ hybridization analysis. Preimplantation Genetic Group. Fertil Steril 1996; 66:126-129.
-
(1996)
Fertil Steril
, vol.66
, pp. 126-129
-
-
Verlinsky, Y.1
Cieslak, J.2
Ivakhnenko, V.3
Lifchez, A.4
Strom, C.5
Kuliev, A.6
-
4
-
-
6844221392
-
Cleavage stage human embryo biopsy
-
Ao A, Handyside AH. Cleavage stage human embryo biopsy. Hum Reprod Update 1995; 1:3-4.
-
(1995)
Hum Reprod Update
, vol.1
, pp. 3-4
-
-
Ao, A.1
Handyside, A.H.2
-
5
-
-
0025180503
-
Human preimplantation development in vitro is not adversely affected by biopsy at the 8-cell stage
-
Hardy K, Martin KL, Leese HJ, Winston RM, Handyside AH. Human preimplantation development in vitro is not adversely affected by biopsy at the 8-cell stage. Hum Reprod 1990; 5:708-714.
-
(1990)
Hum Reprod
, vol.5
, pp. 708-714
-
-
Hardy, K.1
Martin, K.L.2
Leese, H.J.3
Winston, R.M.4
Handyside, A.H.5
-
6
-
-
0025081181
-
Trophecto-derm biopsy in human blastocysts
-
Dokras A, Sargent IL, Ross C, Gardner RL, Barlow DH. Trophecto-derm biopsy in human blastocysts. Hum Reprod 1990; 5:821-825.
-
(1990)
Hum Reprod
, vol.5
, pp. 821-825
-
-
Dokras, A.1
Sargent, I.L.2
Ross, C.3
Gardner, R.L.4
Barlow, D.H.5
-
7
-
-
0027731567
-
Biopsy of the human blastocyst and polymerase chain reaction (Pcr) amplification of the beta-globin gene and a dinucleotide repeat motif from 2-6 trophecto-derm cells
-
Muggleton Harris AL, Glazier AM, Pickering SJ. Biopsy of the human blastocyst and polymerase chain reaction (PCR) amplification of the beta-globin gene and a dinucleotide repeat motif from 2-6 trophecto-derm cells. Hum Reprod 1993; 8:2197-2205.
-
(1993)
Hum Reprod
, vol.8
, pp. 2197-2205
-
-
Muggleton Harris, A.L.1
Glazier, A.M.2
Pickering, S.J.3
-
8
-
-
0029044112
-
Reliability and accuracy of polymerase chain reaction amplification of two unique target sequences from biopsies of cleavage-stage and blastocyst-stage human embryos
-
Pickering SJ, Muggleton Harris AL. Reliability and accuracy of polymerase chain reaction amplification of two unique target sequences from biopsies of cleavage-stage and blastocyst-stage human embryos. Hum Reprod 1995; 10:1021-1029.
-
(1995)
Hum Reprod
, vol.10
, pp. 1021-1029
-
-
Pickering, S.J.1
Muggleton Harris, A.L.2
-
9
-
-
0031267915
-
Laser blastocyst biopsy for preimplantation diagnosis in the human
-
Veiga A, Sandalinas M, Benkhalifa M, Boada M, Carrera M, Santalo J, Barri PN, Menezo Y. Laser blastocyst biopsy for preimplantation diagnosis in the human. Zygote 1997; 5:351-354.
-
(1997)
Zygote
, vol.5
, pp. 351-354
-
-
Veiga, A.1
Sandalinas, M.2
Benkhalifa, M.3
Boada, M.4
Carrera, M.5
Santalo, J.6
Barri, P.N.7
Menezo, Y.8
-
10
-
-
0032422202
-
A prospective randomized trial of blastocyst culture and transfer in in-vitro fertilization [see comments]
-
Gardner DK, Schoolcraft WB, Wagley L, Schlenker T, Stevens J, Hesla J. A prospective randomized trial of blastocyst culture and transfer in in-vitro fertilization [see comments]. Hum Reprod 1998; 13:3434-3440.
-
(1998)
Hum Reprod
, vol.13
, pp. 3434-3440
-
-
Gardner, D.K.1
Schoolcraft, W.B.2
Wagley, L.3
Schlenker, T.4
Stevens, J.5
Hesla, J.6
-
11
-
-
0031905759
-
Culture and transfer of human blastocysts increases implantation rates and reduces the need for multiple embryo transfers
-
Gardner DK, Vella P, Lane M, Wagley L, Schlenker T, Schoolcraft WB. Culture and transfer of human blastocysts increases implantation rates and reduces the need for multiple embryo transfers. Fertil Steril 1998; 69:84-88.
-
(1998)
Fertil Steril
, vol.69
, pp. 84-88
-
-
Gardner, D.K.1
Vella, P.2
Lane, M.3
Wagley, L.4
Schlenker, T.5
Schoolcraft, W.B.6
-
13
-
-
0002198654
-
Cleavage stage biopsy of human embryos and diagnosis of x-linked recessive disease
-
Edwards RG, ed., Cambridge, UK: Cambridge University Press
-
Handyside AH, Delhanty JDA. Cleavage stage biopsy of human embryos and diagnosis of X-linked recessive disease. In: Edwards RG, ed. Preimplantation Diagnosis of Human Genetic Disease. Cambridge, UK: Cambridge University Press, 1993:239-270.
-
(1993)
Preimplantation Diagnosis of Human Genetic Disease
, pp. 239-270
-
-
Handyside, A.H.1
Delhanty, J.D.A.2
-
14
-
-
0030022185
-
Identifying the sex of human preimplantation embryos in x-linked disease: Amplification efficiency of a y-specific alphoid repeat from single blastomeres with two lysis protocols
-
Kontogianni EH, Griffin DK, Handyside AH. Identifying the sex of human preimplantation embryos in X-linked disease: amplification efficiency of a Y-specific alphoid repeat from single blastomeres with two lysis protocols. J Assist Reprod Genet 1996; 13:125-132.
-
(1996)
J Assist Reprod Genet
, vol.13
, pp. 125-132
-
-
Kontogianni, E.H.1
Griffin, D.K.2
Handyside, A.H.3
-
15
-
-
0027178898
-
Preimplantation prevention of x-linked disease: Reliable and rapid sex determination of single human cells by restriction analysis of simultaneously amplified zfx and zfy sequences
-
Chong SS, Kristjansson K, Cota J, Handyside AH, Hughes MR. Preimplantation prevention of X-linked disease: reliable and rapid sex determination of single human cells by restriction analysis of simultaneously amplified ZFX and ZFY sequences. Hum Mol Genet 1993; 2:1187-1191.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1187-1191
-
-
Chong, S.S.1
Kristjansson, K.2
Cota, J.3
Handyside, A.H.4
Hughes, M.R.5
-
16
-
-
0025886371
-
Absence of fetal cells in maternal circulation at a level of 1 in 25,000
-
Nakagome Y, Seki S, Nagafuchi S, Nakahori Y, Sato K. Absence of fetal cells in maternal circulation at a level of 1 in 25,000. Am J Med Genet 1991; 40:506-508.
-
(1991)
Am J Med Genet
, vol.40
, pp. 506-508
-
-
Nakagome, Y.1
Seki, S.2
Nagafuchi, S.3
Nakahori, Y.4
Sato, K.5
-
17
-
-
0028211060
-
Amplification of x- and y-chromosome-specific regions from single human blastomeres by polymerase chain reaction for sexing of preimplantation embryos
-
Liu J, Lissens W, Devroey P, Van Steirteghem A, Liebaers I. Amplification of X- and Y-chromosome-specific regions from single human blastomeres by polymerase chain reaction for sexing of preimplantation embryos. Hum Reprod 1994; 9:716-720.
-
(1994)
Hum Reprod
, vol.9
, pp. 716-720
-
-
Liu, J.1
Lissens, W.2
Devroey, P.3
Van Steirteghem, A.4
Liebaers, I.5
-
18
-
-
0023740326
-
Incidence of early loss of pregnancy
-
Wilcox AJ, Weinberg CR, O’Connor JF, Baird DD, Schlatterer JP, Canfield RE, Armstrong EG, Nisula BC. Incidence of early loss of pregnancy. N Engl J Med 1988; 319:189-194.
-
(1988)
N Engl J Med
, vol.319
, pp. 189-194
-
-
Wilcox, A.J.1
Weinberg, C.R.2
O’Connor, J.F.3
Baird, D.D.4
Schlatterer, J.P.5
Canfield, R.E.6
Armstrong, E.G.7
Nisula, B.C.8
-
20
-
-
0025086138
-
Cytogenetic analysis of 750 spontaneous abortions with the direct-preparation method of chorionic villi and its implications for studying genetic causes of pregnancy wastage
-
Eiben B, Bartels I, Bahr-Porsch S, Borgmann S, Gatz G, Gellert G, Goebel R, Hammans W, Hentemann M, Osmers R. Cytogenetic analysis of 750 spontaneous abortions with the direct-preparation method of chorionic villi and its implications for studying genetic causes of pregnancy wastage. Am J Hum Genet 1990; 47:656-663.
-
(1990)
Am J Hum Genet
, vol.47
, pp. 656-663
-
-
Eiben, B.1
Bartels, I.2
Bahr-Porsch, S.3
Borgmann, S.4
Gatz, G.5
Gellert, G.6
Goebel, R.7
Hammans, W.8
Hentemann, M.9
Osmers, R.10
-
21
-
-
0000049938
-
Chromosome abnormalities in human reproductive wastage
-
Hassold TJ. Chromosome abnormalities in human reproductive wastage. Trends Genet 1986; 2:105-110.
-
(1986)
Trends Genet
, vol.2
, pp. 105-110
-
-
Hassold, T.J.1
-
22
-
-
0019498505
-
Avortements spontanes et anomalies chromosomiques parentales: Etude cytogenetique de 248 couples
-
Trochet-Royer CB, Sele B, Jalbert P, Pison H, Racinet C, Bernard P. Avortements spontanes et anomalies chromosomiques parentales: etude cytogenetique de 248 couples. Re Fr Gynecol Obstet 1981; 76: 195-199.
-
(1981)
Re Fr Gynecol Obstet
, vol.76
, pp. 195-199
-
-
Trochet-Royer, C.B.1
Sele, B.2
Jalbert, P.3
Pison, H.4
Racinet, C.5
Bernard, P.6
-
23
-
-
0030058258
-
Advanced maternal age and the risk of down syndrome characterized by the meiotic stage of chromosomal error: A population-based study
-
Yoon PW, Freeman SB, Sherman SL, Taft LF, Gu Y, Pettay D, Flanders WD, Khoury MJ, Hassold TJ. Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study. Am J Hum Genet 1996; 58:628-633.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 628-633
-
-
Yoon, P.W.1
Freeman, S.B.2
Sherman, S.L.3
Taft, L.F.4
Gu, Y.5
Pettay, D.6
Flanders, W.D.7
Khoury, M.J.8
Hassold, T.J.9
-
24
-
-
0023808930
-
Chromosome anomalies in human oocytes failing to fertilize after insemination in vitro
-
Bongso A, Chye NS, Ratnam S, Sathananthan H, Wong PC. Chromosome anomalies in human oocytes failing to fertilize after insemination in vitro. Hum Reprod 1988; 3:645-649.
-
(1988)
Hum Reprod
, vol.3
, pp. 645-649
-
-
Bongso, A.1
Chye, N.S.2
Ratnam, S.3
Sathananthan, H.4
Wong, P.C.5
-
25
-
-
0022997896
-
Chromosomal analysis of unfertilized human oocytes
-
Martin RH, MaHadevan MM, Taylor PJ, Hildebrand K, Long-Simpson L, Peterson D, Yamamoto J, Fleetham J. Chromosomal analysis of unfertilized human oocytes. J Reprod Fertil 1986; 78:673-678.
-
(1986)
J Reprod Fertil
, vol.78
, pp. 673-678
-
-
Martin, R.H.1
MaHadevan, M.M.2
Taylor, P.J.3
Hildebrand, K.4
Long-Simpson, L.5
Peterson, D.6
Yamamoto, J.7
Fleetham, J.8
-
26
-
-
0023943871
-
Assessment of aneuploidy in the human female by using cytogenetics of ivf failures
-
Pellestor F, Sele B. Assessment of aneuploidy in the human female by using cytogenetics of IVF failures. Am J Hum Genet 1988; 42:274-283.
-
(1988)
Am J Hum Genet
, vol.42
, pp. 274-283
-
-
Pellestor, F.1
Sele, B.2
-
27
-
-
0023124952
-
Chromosome investigations in early life. Ii. Human preimplantation embryos
-
Plachot M, Junca AM, Mandelbaum J, de Grouchy J, Salat Baroux J, Cohen J. Chromosome investigations in early life. II. Human preimplantation embryos. Hum Reprod 1987; 2:29-35.
-
(1987)
Hum Reprod
, vol.2
, pp. 29-35
-
-
Plachot, M.1
Junca, A.M.2
Mandelbaum, J.3
De Grouchy, J.4
Salat Baroux, J.5
Cohen, J.6
-
28
-
-
0023785745
-
Cytogenetic analysis of living human oocytes: Cellular basis and developmental consequences of perturbations in chromosomal organization and complement
-
Van Blerkom J, Henry G. Cytogenetic analysis of living human oocytes: cellular basis and developmental consequences of perturbations in chromosomal organization and complement. Hum Reprod 1988; 3: 777-790.
-
(1988)
Hum Reprod
, vol.3
, pp. 777-790
-
-
Van Blerkom, J.1
Henry, G.2
-
29
-
-
0020625695
-
Chromosome abnormalities in human embryos after in vitro fertilization
-
Angell RR, Aitken RJ, van Look PF, Lumsden MA, Templeton AA. Chromosome abnormalities in human embryos after in vitro fertilization. Nature 1983; 303:336-338.
-
(1983)
Nature
, vol.303
, pp. 336-338
-
-
Angell, R.R.1
Aitken, R.J.2
Van Look, P.F.3
Lumsden, M.A.4
Templeton, A.A.5
-
30
-
-
0022487168
-
Chromosome studies in human in vitro fertilization
-
Angell RR, Templeton AA, Aitken RJ. Chromosome studies in human in vitro fertilization. Hum Genet 1986; 72:333-339.
-
(1986)
Hum Genet
, vol.72
, pp. 333-339
-
-
Angell, R.R.1
Templeton, A.A.2
Aitken, R.J.3
-
31
-
-
0002578047
-
Morphologic cytologic and cytogenetic studies of human embryos obtained by ivf
-
Ratnam SS, Teon ES, eds., Lancs, England: Parthenon Publishing Group
-
Plachot M, Mandelbaum J, Junca AM, de Grouchy J, Cohen J, Salat Baroux J, Da Lage C. Morphologic cytologic and cytogenetic studies of human embryos obtained by IVF. In: Ratnam SS, Teon ES, eds. In-vitro fertilization: Proceedings of the 12th World Congress on Fertility and Sterility. Lancs, England: Parthenon Publishing Group, 1986:61-65.
-
(1986)
In-Vitro Fertilization: Proceedings of the 12Th World Congress on Fertility and Sterility
, pp. 61-65
-
-
Plachot, M.1
Mandelbaum, J.2
Junca, A.M.3
De Grouchy, J.4
Cohen, J.5
Salat Baroux, J.6
Da Lage, C.7
-
32
-
-
0026573160
-
Cytogenetics of human oocytes, zygotes, and embryos after in vitro fertilization
-
Zenzes MT, Casper RF. Cytogenetics of human oocytes, zygotes, and embryos after in vitro fertilization. Hum Genet 1992; 88:367-375.
-
(1992)
Hum Genet
, vol.88
, pp. 367-375
-
-
Zenzes, M.T.1
Casper, R.F.2
-
33
-
-
0027997527
-
Presence of chromosomal mosaicism in abnormal human preimplantation embryos detected by fluorescent in situ hybridization (Fish)
-
Coonen E, Harper JC, Ramaekers FCS, Delhanty JDA, Hopman AHN, Geraedts JPM, Handyside AH. Presence of chromosomal mosaicism in abnormal human preimplantation embryos detected by fluorescent in situ hybridization (FISH). Hum Genet 1994; 54:609-615.
-
(1994)
Hum Genet
, vol.54
, pp. 609-615
-
-
Coonen, E.1
Harper, J.C.2
Ramaekers, F.3
Delhanty, J.4
Hopman, A.5
Geraedts, J.6
Handyside, A.H.7
-
35
-
-
0029067710
-
Embryo morphology, developmental rates, and maternal age are correlated with chromosome abnormalities
-
Munne S, Alikani M, Tomkin G, Grifo J, Cohen J. Embryo morphology, developmental rates, and maternal age are correlated with chromosome abnormalities. Fertil Steril 1995; 64:382-391.
-
(1995)
Fertil Steril
, vol.64
, pp. 382-391
-
-
Munne, S.1
Alikani, M.2
Tomkin, G.3
Grifo, J.4
Cohen, J.5
-
36
-
-
0032901686
-
Preimplantation genetic diagnosis of an-euploidy: Were we looking at the wrong chromosomes?
-
Bahce M, Cohen J, Munne S. Preimplantation genetic diagnosis of an-euploidy: were we looking at the wrong chromosomes? J Assist Reprod Genet 1999; 16:176-181.
-
(1999)
J Assist Reprod Genet
, vol.16
, pp. 176-181
-
-
Bahce, M.1
Cohen, J.2
Munne, S.3
-
37
-
-
0028141729
-
Chromosome abnormalities in human arrested preimplantation embryos: A multiple-probe fish study
-
Munne S, Grifo J, Cohen J, Weier HU. Chromosome abnormalities in human arrested preimplantation embryos: a multiple-probe FISH study. Am J Hum Genet 1994; 55:150-159.
-
(1994)
Am J Hum Genet
, vol.55
, pp. 150-159
-
-
Munne, S.1
Grifo, J.2
Cohen, J.3
Weier, H.U.4
-
38
-
-
0028816762
-
Mosaicism of autosomes and sex chromosomes in morphologically normal, monospermic preimplantation human embryos
-
Harper JC, Coonen E, Handyside AH, Winston RM, Hopman AH, Delhanty JD. Mosaicism of autosomes and sex chromosomes in morphologically normal, monospermic preimplantation human embryos. Prenat Diagn 1995; 15:41-49.
-
(1995)
Prenat Diagn
, vol.15
, pp. 41-49
-
-
Harper, J.C.1
Coonen, E.2
Handyside, A.H.3
Winston, R.M.4
Hopman, A.H.5
Delhanty, J.D.6
-
39
-
-
0030059516
-
Cytogenetics of uncleaved oocytes and arrested zygotes in ivf programs
-
Benkhalifa M, Menezo Y, Janny L, Pouly JL, Qumsiyeh MB. Cytogenetics of uncleaved oocytes and arrested zygotes in IVF programs. J Assist Reprod Genet 1996; 13:140-148.
-
(1996)
J Assist Reprod Genet
, vol.13
, pp. 140-148
-
-
Benkhalifa, M.1
Menezo, Y.2
Janny, L.3
Pouly, J.L.4
Qumsiyeh, M.B.5
-
40
-
-
0029893780
-
The relationship between chromosomal abnormality in the human preimplantation embryo and development in vitro
-
Almeida PA, Bolton VN. The relationship between chromosomal abnormality in the human preimplantation embryo and development in vitro. Reprod Fertil Dev 1996; 8:235-241.
-
(1996)
Reprod Fertil Dev
, vol.8
, pp. 235-241
-
-
Almeida, P.A.1
Bolton, V.N.2
-
41
-
-
0031009264
-
Multicolour fish detects frequent chromosomal mosaicism and chaotic division in normal preimplantation embryos from fertile patients
-
Delhanty JD, Harper JC, Ao A, Handyside AH, Winston RM. Multicolour FISH detects frequent chromosomal mosaicism and chaotic division in normal preimplantation embryos from fertile patients. Hum Genet 1997; 99:755-760.
-
(1997)
Hum Genet
, vol.99
, pp. 755-760
-
-
Delhanty, J.D.1
Harper, J.C.2
Ao, A.3
Handyside, A.H.4
Winston, R.M.5
-
42
-
-
0033868950
-
Chromosome mosaicism in day 3 aneuploid embryos that develop to morphologically normal blastocysts in vitro
-
Magli MC, Jones GM, Gras L, Gianaroli L, Korman I, Trounson AO. Chromosome mosaicism in day 3 aneuploid embryos that develop to morphologically normal blastocysts in vitro. Hum Reprod 2000; 15: 1781-1786.
-
(2000)
Hum Reprod
, vol.15
, pp. 1781-1786
-
-
Magli, M.C.1
Jones, G.M.2
Gras, L.3
Gianaroli, L.4
Korman, I.5
Trounson, A.O.6
-
43
-
-
0029859590
-
Preimplantation embryo chromosome analysis by primed in situ labeling method [published erratum appears in fertil steril 1997; 67:591]
-
Pellestor F, Girardet A, Andreo B, Lefort G, Charlieu JP. Preimplantation embryo chromosome analysis by primed in situ labeling method [published erratum appears in Fertil Steril 1997; 67:591]. Fertil Steril 1996; 66:781-786.
-
(1996)
Fertil Steril
, vol.66
, pp. 781-786
-
-
Pellestor, F.1
Girardet, A.2
Reo, B.3
Lefort, G.4
Charlieu, J.P.5
-
44
-
-
0029997093
-
Association between nondisjunction and maternal age in meiosis-ii human oocytes
-
Dailey T, Dale B, Cohen J, Munne S. Association between nondisjunction and maternal age in meiosis-II human oocytes. Am J Hum Genet 1996; 59:176-184.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 176-184
-
-
Dailey, T.1
Dale, B.2
Cohen, J.3
Munne, S.4
-
45
-
-
0030015876
-
Aneuploidy 16 in human embryos increases significantly with maternal age
-
Benadiva CA, Kligman I, Munne S. Aneuploidy 16 in human embryos increases significantly with maternal age. Fertil Steril 1996; 66:248-255.
-
(1996)
Fertil Steril
, vol.66
, pp. 248-255
-
-
Benadiva, C.A.1
Kligman, I.2
Munne, S.3
-
46
-
-
0026642082
-
Cumulative conception and livebirth rates after in-vitro fertilisation [see comments]
-
Tan SL, Royston P, Campbell S, Jacobs HS, Betts J, Mason B, Edwards RG. Cumulative conception and livebirth rates after in-vitro fertilisation [see comments]. Lancet 1992; 339:1390-1394.
-
(1992)
Lancet
, vol.339
, pp. 1390-1394
-
-
Tan, S.L.1
Royston, P.2
Campbell, S.3
Jacobs, H.S.4
Betts, J.5
Mason, B.6
Edwards, R.G.7
-
47
-
-
0029111671
-
Pregnancies following pre-conception diagnosis of common aneuploidies by fluorescent in-situ hybridization
-
Verlinsky Y, Cieslak J, Freidine M, Ivakhnenko V, Wolf G, Kovalin-skaya L, White M, Lifchez A, Kaplan B, Moise J. Pregnancies following pre-conception diagnosis of common aneuploidies by fluorescent in-situ hybridization. Hum Reprod 1995; 10:1923-1927.
-
(1995)
Hum Reprod
, vol.10
, pp. 1923-1927
-
-
Verlinsky, Y.1
Cieslak, J.2
Freidine, M.3
Ivakhnenko, V.4
Wolf, G.5
Kovalin-Skaya, L.6
White, M.7
Lifchez, A.8
Kaplan, B.9
Moise, J.10
-
48
-
-
0029827235
-
Preimplantation diagnosis of common aneu-ploidies in infertile couples of advanced maternal age
-
Verlinsky Y, Kuliev A. Preimplantation diagnosis of common aneu-ploidies in infertile couples of advanced maternal age. Hum Reprod 1996; 11:2076-2077.
-
(1996)
Hum Reprod
, vol.11
, pp. 2076-2077
-
-
Verlinsky, Y.1
Kuliev, A.2
-
49
-
-
0032701590
-
Preimplantation diagnosis for aneuploidies in patients undergoing in vitro fertilization with a poor prognosis: Identification of the categories for which it should be proposed
-
Gianaroli L, Magli MC, Ferraretti AP, Munne S. Preimplantation diagnosis for aneuploidies in patients undergoing in vitro fertilization with a poor prognosis: identification of the categories for which it should be proposed. Fertil Steril 1999; 72:837-844.
-
(1999)
Fertil Steril
, vol.72
, pp. 837-844
-
-
Gianaroli, L.1
Magli, M.C.2
Ferraretti, A.P.3
Munne, S.4
-
50
-
-
0032835575
-
Positive outcome after preimplantation diagnosis of aneuploidy in human embryos
-
Munne S, Magli C, Cohen J, Morton P, Sadowy S, Gianaroli L, Tucker M, Marquez C, Sable D, Ferraretti AP, Massey JB, Scott R. Positive outcome after preimplantation diagnosis of aneuploidy in human embryos. Hum Reprod 1999; 14:2191-2199.
-
(1999)
Hum Reprod
, vol.14
, pp. 2191-2199
-
-
Munne, S.1
Magli, C.2
Cohen, J.3
Morton, P.4
Sadowy, S.5
Gianaroli, L.6
Tucker, M.7
Marquez, C.8
Sable, D.9
Ferraretti, A.P.10
Massey, J.B.11
Scott, R.12
-
51
-
-
0032903719
-
Prevention of age-related aneuploidies by polar body testing of oocytes
-
Verlinsky Y, Cieslak J, Ivakhnenko V, Evsikov S, Wolf G, White M, Lifchez A, Kaplan B, Moise J, Valle J, Ginsberg N, Strom C, Kuliev A. Prevention of age-related aneuploidies by polar body testing of oocytes. J Assist Reprod Genet 1999; 16:165-169.
-
(1999)
J Assist Reprod Genet
, vol.16
, pp. 165-169
-
-
Verlinsky, Y.1
Cieslak, J.2
Ivakhnenko, V.3
Evsikov, S.4
Wolf, G.5
White, M.6
Lifchez, A.7
Kaplan, B.8
Moise, J.9
Valle, J.10
Ginsberg, N.11
Strom, C.12
Kuliev, A.13
-
52
-
-
7144254459
-
Preimplantation diagnosis of common aneuploidies by the first- and second-polar body fish analysis
-
Verlinsky Y, Cieslak J, Ivakhnenko V, Evsikov S, Wolf G, White M, Lifchez A, Kaplan B, Moise J, Valle J, Ginsberg N, Strom C, Kuliev A. Preimplantation diagnosis of common aneuploidies by the first- and second-polar body FISH analysis. J Assist Reprod Genet 1998; 15: 285-289.
-
(1998)
J Assist Reprod Genet
, vol.15
, pp. 285-289
-
-
Verlinsky, Y.1
Cieslak, J.2
Ivakhnenko, V.3
Evsikov, S.4
Wolf, G.5
White, M.6
Lifchez, A.7
Kaplan, B.8
Moise, J.9
Valle, J.10
Ginsberg, N.11
Strom, C.12
Kuliev, A.13
-
53
-
-
0033918113
-
Obstetric outcomes in 102 pregnancies after preimplantation genetic diagnosis
-
Strom CM, Strom S, Levine E, Ginsberg N, Barton J, Verlinsky Y. Obstetric outcomes in 102 pregnancies after preimplantation genetic diagnosis. Am J Obstet Gynecol 2000; 182:1629-1632.
-
(2000)
Am J Obstet Gynecol
, vol.182
, pp. 1629-1632
-
-
Strom, C.M.1
Strom, S.2
Levine, E.3
Ginsberg, N.4
Barton, J.5
Verlinsky, Y.6
-
54
-
-
0024591981
-
The nonrandom participation of human acrocentric chromosomes in robertsonian translocations
-
Therman E, Susman B, Denniston C. The nonrandom participation of human acrocentric chromosomes in Robertsonian translocations. Ann Hum Genet 1989; 53(pt 1):49-65.
-
(1989)
Ann Hum Genet
, vol.53
, pp. 49-65
-
-
Therman, E.1
Susman, B.2
Denniston, C.3
-
55
-
-
0031977265
-
First pregnancies after preconception diagnosis of translocations of maternal origin
-
Munne S, Scott R, Sable D, Cohen J. First pregnancies after preconception diagnosis of translocations of maternal origin. Fertil Steril 1998; 69:675-681.
-
(1998)
Fertil Steril
, vol.69
, pp. 675-681
-
-
Munne, S.1
Scott, R.2
Sable, D.3
Cohen, J.4
-
56
-
-
0031879163
-
Preimplantation genetic analysis of translocations: Case-specific probes for interphase cell analysis
-
Munne S, Fung J, Cassel MJ, Marquez C, Weier HU. Preimplantation genetic analysis of translocations: case-specific probes for interphase cell analysis. Hum Genet 1998; 102:663-674.
-
(1998)
Hum Genet
, vol.102
, pp. 663-674
-
-
Munne, S.1
Fung, J.2
Cassel, M.J.3
Marquez, C.4
Weier, H.U.5
-
57
-
-
0031922774
-
Infertile couples with robertsonian translocations: Preimplantation genetic analysis of embryos reveals chaotic cleavage divisions
-
Conn CM, Harper JC, Winston RM, Delhanty JD. Infertile couples with Robertsonian translocations: preimplantation genetic analysis of embryos reveals chaotic cleavage divisions. Hum Genet 1998; 102: 117-123.
-
(1998)
Hum Genet
, vol.102
, pp. 117-123
-
-
Conn, C.M.1
Harper, J.C.2
Winston, R.M.3
Delhanty, J.D.4
-
58
-
-
0033999881
-
Preimplantation genetic diagnosis of a reciprocal translocation t(3;11)(q27.3;q24.3) in siblings
-
Coonen E, Martini E, Dumoulin JC, Hollanders-Crombach HT, de Die-Smulders C, Geraedts JP, Hopman AH, Evers JL. Preimplantation genetic diagnosis of a reciprocal translocation t(3;11)(q27.3;q24.3) in siblings. Mol Hum Reprod 2000; 6:199-206.
-
(2000)
Mol Hum Reprod
, vol.6
, pp. 199-206
-
-
Coonen, E.1
Martini, E.2
Dumoulin, J.C.3
Hollanders-Crombach, H.T.4
De Die-Smulders, C.5
Geraedts, J.P.6
Hopman, A.H.7
Evers, J.L.8
-
59
-
-
0033939598
-
Clinical pregnancy following blastomere biopsy and pgd for a reciprocal translocation carrier: Analysis of meiotic outcomes and embryo quality in two ivf cycles
-
Scriven PN, O’Mahony F, Bickerstaff H, Yeong CT, Braude P, Mackie OC. Clinical pregnancy following blastomere biopsy and PGD for a reciprocal translocation carrier: analysis of meiotic outcomes and embryo quality in two IVF cycles. Prenat Diagn 2000; 20:587-592.
-
(2000)
Prenat Diagn
, vol.20
, pp. 587-592
-
-
Scriven, P.N.1
O’Mahony, F.2
Bickerstaff, H.3
Yeong, C.T.4
Braude, P.5
Mackie, O.C.6
-
61
-
-
0032756727
-
Eshre preimplantation genetic diagnosis (Pgd) consortium: Preliminary assessment of data from january 1997 to september 1998. Eshre pgd consortium steering committee
-
Geraedts J, Handyside A, Harper J, Liebaers I, Sermon K, Staessen C, Thornhill A, Vanderfaeillie A, Viville S. ESHRE Preimplantation Genetic Diagnosis (PGD) Consortium: preliminary assessment of data from January 1997 to September 1998. ESHRE PGD Consortium Steering Committee. Hum Reprod 1999; 14:3138-3148.
-
(1999)
Hum Reprod
, vol.14
, pp. 3138-3148
-
-
Geraedts, J.1
Handyside, A.2
Harper, J.3
Liebaers, I.4
Sermon, K.5
Staessen, C.6
Thornhill, A.7
Vanderfaeillie, A.8
Viville, S.9
-
62
-
-
0022924142
-
The genetic aspects of neurofibromatosis
-
Carey JC, Baty BJ, Johnson JP, Morrison T, Skolnick M, Kivlin J. The genetic aspects of neurofibromatosis. Ann NY Acad Sci 1986; 486:4556.
-
(1986)
Ann NY Acad Sci
, vol.486
, pp. 4556
-
-
Carey, J.C.1
Baty, B.J.2
Johnson, J.P.3
Morrison, T.4
Skolnick, M.5
Kivlin, J.6
-
63
-
-
0026345716
-
Variation of the cgg repeat at the fragile x site results in genetic instability: Resolution of the sherman paradox
-
Fu YH, Kuhl DP, Pizzuti A, Pieretti M, Sutcliffe JS, Richards S, Verkerk AJ, Holden JJ, Fenwick RGJ, Warren ST, et al. Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox. Cell 1991; 67:1047-1058.
-
(1991)
Cell
, vol.67
, pp. 1047-1058
-
-
Fu, Y.H.1
Kuhl, D.P.2
Pizzuti, A.3
Pieretti, M.4
Sutcliffe, J.S.5
Richards, S.6
Verkerk, A.J.7
Holden, J.J.8
Fenwick, R.9
Warren, S.T.10
-
64
-
-
0025912402
-
Hereditary unstable dna: A new explanation for some old genetic questions?
-
Sutherland GR, Haan EA, Kremer E, Lynch M, Pritchard M, Yu S, Richards RI. Hereditary unstable DNA: a new explanation for some old genetic questions? Lancet 1991; 338:289-292.
-
(1991)
Lancet
, vol.338
, pp. 289-292
-
-
Sutherland, G.R.1
Haan, E.A.2
Kremer, E.3
Lynch, M.4
Pritchard, M.5
Yu, S.6
Richards, R.I.7
-
65
-
-
0026347628
-
Fragile x genotype characterized by an unstable region of dna
-
Yu S, Pritchard M, Kremer E, Lynch M, Nancarrow J, Baker E, Holman K, Mulley JC, Warren ST, Schlessinger D, et al. Fragile X genotype characterized by an unstable region of DNA. Science 1991; 252:1179-1181.
-
(1991)
Science
, vol.252
, pp. 1179-1181
-
-
Yu, S.1
Pritchard, M.2
Kremer, E.3
Lynch, M.4
Nancarrow, J.5
Baker, E.6
Holman, K.7
Mulley, J.C.8
Warren, S.T.9
Schlessinger, D.10
-
66
-
-
0029584496
-
Trinucleotide repeat expansion and human disease. [review]
-
Ashley CT Jr, Warren ST. Trinucleotide repeat expansion and human disease. [Review]. Ann Rev Genet 1995; 29:703-728.
-
(1995)
Ann Rev Genet
, vol.29
, pp. 703-728
-
-
Ashley, C.T.1
Warren, S.T.2
-
67
-
-
0030793199
-
Trinucleotide repeat instability: Genetic features and molecular mechanisms. [review]
-
La Spada AR. Trinucleotide repeat instability: genetic features and molecular mechanisms. [Review]. Brain Pathol 1997; 7:943-963.
-
(1997)
Brain Pathol
, vol.7
, pp. 943-963
-
-
La Spada, A.R.1
-
68
-
-
0026713048
-
Birth of a normal girl after in vitro fertilization and preimplantation diagnostic testing for cystic fibrosis
-
Handyside AH, Lesko JG, Tarin JJ, Winston RML, Hughes MR. Birth of a normal girl after in vitro fertilization and preimplantation diagnostic testing for cystic fibrosis. N Engl J Med 1992; 327:905-909.
-
(1992)
N Engl J Med
, vol.327
, pp. 905-909
-
-
Handyside, A.H.1
Lesko, J.G.2
Tarin, J.J.3
Winston, R.4
Hughes, M.R.5
-
69
-
-
13344284633
-
Clinical experience with preimplantation genetic diagnosis of cystic fibrosis (Delta f508)
-
Ao A, Ray P, Harper J, Lesko J, Paraschos T, Atkinson G, Soussis I, Taylor D, Handyside A, Hughes M, Winston RM. Clinical experience with preimplantation genetic diagnosis of cystic fibrosis (delta F508). Prenat Diagn 1996; 16:137-142.
-
(1996)
Prenat Diagn
, vol.16
, pp. 137-142
-
-
Ao, A.1
Ray, P.2
Harper, J.3
Lesko, J.4
Paraschos, T.5
Atkinson, G.6
Soussis, I.7
Taylor, D.8
Handyside, A.9
Hughes, M.10
Winston, R.M.11
-
71
-
-
7144253137
-
Preimplantation diagnosis of thalassemias
-
Kuliev A, Rechitsky S, Verlinsky O, Ivakhnenko V, Evsikov S, Wolf G, Angastiniotis M, Georghiou D, Kukharenko V, Strom C, Verlinsky Y. Preimplantation diagnosis of thalassemias. J Assist Reprod Genet 1998; 15:219-225.
-
(1998)
J Assist Reprod Genet
, vol.15
, pp. 219-225
-
-
Kuliev, A.1
Rechitsky, S.2
Verlinsky, O.3
Ivakhnenko, V.4
Evsikov, S.5
Wolf, G.6
Angastiniotis, M.7
Georghiou, D.8
Kukharenko, V.9
Strom, C.10
Verlinsky, Y.11
-
72
-
-
0032948199
-
Birth of healthy children after preimplantation diagnosis of thalassemias
-
Kuliev A, Rechitsky S, Verlinsky O, Ivakhnenko V, Cieslak J, Evsikov S, Wolf G, Angastiniotis M, Kalakoutis G, Strom C, Verlinsky Y. Birth of healthy children after preimplantation diagnosis of thalassemias. J Assist Reprod Genet 1999; 16:207-211.
-
(1999)
J Assist Reprod Genet
, vol.16
, pp. 207-211
-
-
Kuliev, A.1
Rechitsky, S.2
Verlinsky, O.3
Ivakhnenko, V.4
Cieslak, J.5
Evsikov, S.6
Wolf, G.7
Angastiniotis, M.8
Kalakoutis, G.9
Strom, C.10
Verlinsky, Y.11
-
73
-
-
0033378762
-
Preimplantation genetic diagnosis in 10 couples at risk for transmitting beta-thalassaemia major: Clinical experience including the initiation of six singleton pregnancies
-
Kanavakis E, Vrettou C, Palmer G, Tzetis M, Mastrominas M, Traeger-Synodinos J. Preimplantation genetic diagnosis in 10 couples at risk for transmitting beta-thalassaemia major: clinical experience including the initiation of six singleton pregnancies. Prenat Diagn 1999; 19: 1217-1222.
-
(1999)
Prenat Diagn
, vol.19
, pp. 1217-1222
-
-
Kanavakis, E.1
Vrettou, C.2
Palmer, G.3
Tzetis, M.4
Mastrominas, M.5
Traeger-Synodinos, J.6
-
74
-
-
0031663165
-
Preimplantation genetic diagnosis of spinal muscular dystrophy
-
Dreesen JC, Bras M, de Die-Smulders C, Dumoulin JC, Cobben JM, Evers JL, Smeets HJ, Geraedts JP. Preimplantation genetic diagnosis of spinal muscular dystrophy. Mol Hum Reprod 1998; 4:881-885.
-
(1998)
Mol Hum Reprod
, vol.4
, pp. 881-885
-
-
Dreesen, J.C.1
Bras, M.2
De Die-Smulders, C.3
Dumoulin, J.C.4
Cobben, J.M.5
Evers, J.L.6
Smeets, H.J.7
Geraedts, J.P.8
-
76
-
-
0026629939
-
Fluorescent multiplex linkage analysis and carrier detection for duchenne/becker muscular dystrophy
-
Schwartz LS, Tarleton J, Popovich B, Seltzer WK, Hoffman EP. Fluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophy. Am J Hum Genet 1992; 51:721-729.
-
(1992)
Am J Hum Genet
, vol.51
, pp. 721-729
-
-
Schwartz, L.S.1
Tarleton, J.2
Popovich, B.3
Seltzer, W.K.4
Hoffman, E.P.5
-
77
-
-
0027138360
-
Duchenne/becker muscular dystrophy carrier detection using quantitative pcr and fluorescence-based strategies
-
Mansfield ES, Robertson JM, Lebo RV, Lucero MY, Mayrand PE, Rappaport E, Parrella T, Sartore M, Surrey S, Fortina P. Duchenne/Becker muscular dystrophy carrier detection using quantitative PCR and fluorescence-based strategies. Am J Med Genet 1993; 48:200-208.
-
(1993)
Am J Med Genet
, vol.48
, pp. 200-208
-
-
Mansfield, E.S.1
Robertson, J.M.2
Lebo, R.V.3
Lucero, M.Y.4
Mayrand, P.E.5
Rappaport, E.6
Parrella, T.7
Sartore, M.8
Surrey, S.9
Fortina, P.10
-
78
-
-
0031440262
-
Accurate sizing of (Cag)n repeats causing huntington disease by fluorescent pcr
-
Toth T, Findlay I, Nagy B, Papp Z. Accurate sizing of (CAG)n repeats causing Huntington disease by fluorescent PCR. Clin Chem 1997; 43: 2422-2423.
-
(1997)
Clin Chem
, vol.43
, pp. 2422-2423
-
-
Toth, T.1
Findlay, I.2
Nagy, B.3
Papp, Z.4
-
79
-
-
0031947004
-
Same day diagnosis of down’s syndrome and sex in single cells using multiplex fluorescent pcr
-
Findlay I, Matthews P, Toth T, Quirke P, Papp Z. Same day diagnosis of Down’s syndrome and sex in single cells using multiplex fluorescent PCR. Mol Pathol 1998; 51:164-167.
-
(1998)
Mol Pathol
, vol.51
, pp. 164-167
-
-
Findlay, I.1
Matthews, P.2
Toth, T.3
Quirke, P.4
Papp, Z.5
-
80
-
-
0031872118
-
Fluorescent pcr and automated fragment analysis for the clinical application of preimplantation genetic diagnosis of myotonic dystrophy (Steinhert’s disease)
-
Sermon K, De Vos A, Van de Velde H, Seneca S, Lissens W, Joris H, Vandervorst M, Van Steirteghem A, Liebaers I. Fluorescent PCR and automated fragment analysis for the clinical application of preimplantation genetic diagnosis of myotonic dystrophy (Steinhert’s disease). Mol Hum Reprod 1998; 4:791-796.
-
(1998)
Mol Hum Reprod
, vol.4
, pp. 791-796
-
-
Sermon, K.1
De Vos, A.2
Van De Velde, H.3
Seneca, S.4
Lissens, W.5
Joris, H.6
Vandervorst, M.7
Van Steirteghem, A.8
Liebaers, I.9
-
81
-
-
0032413395
-
Preimplantation diagnosis for huntington’s disease (Hd): Clinical application and analysis of the hd expansion in affected embryos
-
Sermon K, Goosens V, Seneca S, Lissens W, De Vos A, Vandervorst M, Van Steirteghem A, Liebaers I. Preimplantation diagnosis for Huntington’s disease (HD): clinical application and analysis of the HD expansion in affected embryos. Prenat Diagn 1998; 18:1427-1436.
-
(1998)
Prenat Diagn
, vol.18
, pp. 1427-1436
-
-
Sermon, K.1
Goosens, V.2
Seneca, S.3
Lissens, W.4
De Vos, A.5
Vandervorst, M.6
Van Steirteghem, A.7
Liebaers, I.8
-
83
-
-
0029038302
-
Allelic drop-out and preferential amplification in single cells and human blastomeres: Implications for preimplantation diagnosis of sex and cystic fibrosis
-
Findlay I, Ray P, Quirke P, Rutherford A, Lilford R. Allelic drop-out and preferential amplification in single cells and human blastomeres: implications for preimplantation diagnosis of sex and cystic fibrosis. Hum Reprod 1995; 10:1609-1618.
-
(1995)
Hum Reprod
, vol.10
, pp. 1609-1618
-
-
Findlay, I.1
Ray, P.2
Quirke, P.3
Rutherford, A.4
Lilford, R.5
-
84
-
-
0030776767
-
Clinical application of preimplantation diagnosis for myotonic dystrophy
-
Sermon K, Lissens W, Joris H, Seneca S, Desmyttere S, Devroey P, van Steirteghem A, Liebaers I. Clinical application of preimplantation diagnosis for myotonic dystrophy. Prenat Diagn 1997; 17:925-932.
-
(1997)
Prenat Diagn
, vol.17
, pp. 925-932
-
-
Sermon, K.1
Lissens, W.2
Joris, H.3
Seneca, S.4
Desmyttere, S.5
Devroey, P.6
Van Steirteghem, A.7
Liebaers, I.8
-
85
-
-
0034640011
-
Fourteen and counting: Unraveling trinucleotide repeat diseases
-
Cummings CJ, Zoghbi HY. Fourteen and counting: unraveling trinucleotide repeat diseases. Hum Mol Genet 2000; 9:909-916.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 909-916
-
-
Cummings, C.J.1
Zoghbi, H.Y.2
-
86
-
-
0026566108
-
Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (ctg) repeat at the 3 end of a transcript encoding a protein kinase family member
-
Brook JD, McCurrach ME, Harley HG, Buckler AJ, Church D, Abura-tani H, Hunter K, Stanton VP, Thirion JP, Hudson T. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3 end of a transcript encoding a protein kinase family member. Cell 1992; 68:799-808.
-
(1992)
Cell
, vol.68
, pp. 799-808
-
-
Brook, J.D.1
McCurrach, M.E.2
Harley, H.G.3
Buckler, A.J.4
Church, D.5
Abura-Tani, H.6
Hunter, K.7
Stanton, V.P.8
Thirion, J.P.9
Hudson, T.10
-
87
-
-
0026603841
-
Myotonic dystrophy mutation: An unstable ctg repeat in the 3' untranslated region of the gene
-
Mahadevan M, Tsilfidis C, Sabourin L, Shutler G, Amemiya C, Jansen G, Neville C, Narang M, Barcelo J, O’Hoy K, et al. Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene. Science 1992; 255:1253-1255.
-
(1992)
Science
, vol.255
, pp. 1253-1255
-
-
Mahadevan, M.1
Tsilfidis, C.2
Sabourin, L.3
Shutler, G.4
Amemiya, C.5
Jansen, G.6
Neville, C.7
Narang, M.8
Barcelo, J.9
O’Hoy, K.10
-
88
-
-
0034848136
-
The development of preimplantation genetic diagnosis for myotonic dystrophy using multiplex fluorescent pcr and its clinical application
-
Dean NL, Tan SL, Ao A. The development of preimplantation genetic diagnosis for myotonic dystrophy using multiplex fluorescent PCR and its clinical application. Mol Hum Reprod 2001; 7:895-901.
-
(2001)
Mol Hum Reprod
, vol.7
, pp. 895-901
-
-
Dean, N.L.1
Tan, S.L.2
Ao, A.3
-
89
-
-
0034534916
-
Eshre preimplantation genetic diagnosis (Pgd) consortium: Data collection ii (may 2000)
-
Geraedts J, Handyside A, Harper J, Liebaers I, Sermon K, Staessen C, Thornhill A, Viville S, Wilton L. ESHRE preimplantation genetic diagnosis (PGD) consortium: data collection II (May 2000). Hum Reprod 2000; 15:2673-2683.
-
(2000)
Hum Reprod
, vol.15
, pp. 2673-2683
-
-
Geraedts, J.1
Handyside, A.2
Harper, J.3
Liebaers, I.4
Sermon, K.5
Staessen, C.6
Thornhill, A.7
Viville, S.8
Wilton, L.9
-
90
-
-
0030224254
-
Preimplantation genetic testing for marfan syndrome
-
Harton GL, Tsipouras P, Sisson ME, Starr KM, Mohoney BS, Fugger EF, Schulman JD, Kilpatrick MW, Levinson G, Black SH. Preimplantation genetic testing for Marfan syndrome. Mol Hum Reprod 1996; 2:713-715.
-
(1996)
Mol Hum Reprod
, vol.2
, pp. 713-715
-
-
Harton, G.L.1
Tsipouras, P.2
Sisson, M.E.3
Starr, K.M.4
Mohoney, B.S.5
Fugger, E.F.6
Schulman, J.D.7
Kilpatrick, M.W.8
Levinson, G.9
Black, S.H.10
-
91
-
-
0031924908
-
Preimplantation genetic diagnosis of human embryos for marfan’s syndrome
-
Blaszczyk A, Tang YX, Dietz HC, Adler A, Berkeley AS, Krey LC, Grifo JA. Preimplantation genetic diagnosis of human embryos for Marfan’s syndrome. J Assist Reprod Genet 1998; 15:281-284.
-
(1998)
J Assist Reprod Genet
, vol.15
, pp. 281-284
-
-
Blaszczyk, A.1
Tang, Y.X.2
Dietz, H.C.3
Adler, A.4
Berkeley, A.S.5
Krey, L.C.6
Grifo, J.A.7
-
92
-
-
0032919952
-
Preimplantation genetic diagnosis of marfan syndrome with the use of fluorescent polymerase chain reaction and the automated laser fluorescence dna sequencer
-
Sermon K, Lissens W, Messiaen L, Bonduelle M, Vandervorst M, Van Steirteghem A, Liebaers I. Preimplantation genetic diagnosis of Marfan syndrome with the use of fluorescent polymerase chain reaction and the Automated Laser Fluorescence DNA Sequencer. Fertil Steril 1999; 71:163-166.
-
(1999)
Fertil Steril
, vol.71
, pp. 163-166
-
-
Sermon, K.1
Lissens, W.2
Messiaen, L.3
Bonduelle, M.4
Vandervorst, M.5
Van Steirteghem, A.6
Liebaers, I.7
-
93
-
-
0030016277
-
Attitudes to predictive dna testing in familial adenomatous polyposis
-
Whitelaw S, Northover JM, Hodgson SV. Attitudes to predictive DNA testing in familial adenomatous polyposis. J Med Genet 1996; 33:540-543.
-
(1996)
J Med Genet
, vol.33
, pp. 540-543
-
-
Whitelaw, S.1
Northover, J.M.2
Hodgson, S.V.3
-
94
-
-
6844239539
-
Preimplantation genetic diagnosis of inherited cancer: Familial adenomatous polyposis coli
-
Ao A, Wells D, Handyside AH, Winston RM, Delhanty JD. Preimplantation genetic diagnosis of inherited cancer: familial adenomatous polyposis coli. J Assist Reprod Genet 1998; 15:140-144.
-
(1998)
J Assist Reprod Genet
, vol.15
, pp. 140-144
-
-
Ao, A.1
Wells, D.2
Handyside, A.H.3
Winston, R.M.4
Delhanty, J.D.5
-
95
-
-
0028968665
-
Normal pregnancy after preimplantation dna diagnosis of a dystrophin gene deletion
-
Liu J, Lissens W, Van Broeckhoven C, Lofgren A, Camus M, Liebaers I, Van Steirteghem A. Normal pregnancy after preimplantation DNA diagnosis of a dystrophin gene deletion. Prenat Diagn 1995; 15:351-358.
-
(1995)
Prenat Diagn
, vol.15
, pp. 351-358
-
-
Liu, J.1
Lissens, W.2
Van Broeckhoven, C.3
Lofgren, A.4
Camus, M.5
Liebaers, I.6
Van Steirteghem, A.7
-
96
-
-
0033397941
-
Successful preimplantation genetic diagnosis for sex linked lesch-nyhan syndrome using specific diagnosis
-
Ray PF, Harper JC, Ao A, Taylor DM, Winston RM, Hughes M, Handyside AH. Successful preimplantation genetic diagnosis for sex linked Lesch-Nyhan Syndrome using specific diagnosis. Prenat Diagn 1999; 19:1237-1241.
-
(1999)
Prenat Diagn
, vol.19
, pp. 1237-1241
-
-
Ray, P.F.1
Harper, J.C.2
Ao, A.3
Taylor, D.M.4
Winston, R.M.5
Hughes, M.6
Handyside, A.H.7
-
97
-
-
0033402877
-
Preimplantation diagnosis for fragile x syndrome based on the detection of the non-expanded paternal and maternal cgg
-
Sermon K, Seneca S, Vanderfaeillie A, Lissens W, Joris H, Vander-vorst M, Van Steirteghem A, Liebaers I. Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGG. Prenat Diagn 1999; 19:1223-1230.
-
(1999)
Prenat Diagn
, vol.19
, pp. 1223-1230
-
-
Sermon, K.1
Seneca, S.2
Vanderfaeillie, A.3
Lissens, W.4
Joris, H.5
Vander-Vorst, M.6
Van Steirteghem, A.7
Liebaers, I.8
-
98
-
-
0027752043
-
Co-amplification of the cystic fibrosis delta f508 mutation with the hla dqa1 sequence in single cell pcr: Implications for improved assessment of polar bodies and blastomeres in preimplantation diagnosis
-
Wu R, Cuppens H, Buyse I, Decorte R, Marynen P, Gordts S, Cassiman JJ. Co-amplification of the cystic fibrosis delta F508 mutation with the HLA DQA1 sequence in single cell PCR: implications for improved assessment of polar bodies and blastomeres in preimplantation diagnosis. Prenat Diagn 1993; 13:1111-1122.
-
(1993)
Prenat Diagn
, vol.13
, pp. 1111-1122
-
-
Wu, R.1
Cuppens, H.2
Buyse, I.3
Decorte, R.4
Marynen, P.5
Gordts, S.6
Cassiman, J.J.7
-
99
-
-
0029028913
-
Simultaneous amplification of the two most frequent mutations of infantile tay-sachs disease in single blastomeres
-
Sermon K, Lissens W, Nagy ZP, Van Steirteghem A, Liebaers I. Simultaneous amplification of the two most frequent mutations of infantile Tay-Sachs disease in single blastomeres. Hum Reprod 1995; 10:2214-2217.
-
(1995)
Hum Reprod
, vol.10
, pp. 2214-2217
-
-
Sermon, K.1
Lissens, W.2
Nagy, Z.P.3
Van Steirteghem, A.4
Liebaers, I.5
-
100
-
-
0030039944
-
Polymerase chain reaction amplification specificity: Incidence of allele dropout using different dna preparation methods for heterozygous single cells
-
Gitlin SA, Lanzendorf SE, Gibbons WE. Polymerase chain reaction amplification specificity: incidence of allele dropout using different DNA preparation methods for heterozygous single cells. J Assist Re-prod Genet 1996; 13:107-111.
-
(1996)
J Assist Re-Prod Genet
, vol.13
, pp. 107-111
-
-
Gitlin, S.A.1
Lanzendorf, S.E.2
Gibbons, W.E.3
-
101
-
-
0030089526
-
Increasing the denaturation temperature during the first cycles of amplification reduces allele dropout from single cells for preimplantation genetic diagnosis
-
Ray PF, Handyside AH. Increasing the denaturation temperature during the first cycles of amplification reduces allele dropout from single cells for preimplantation genetic diagnosis. Mol Hum Reprod 1996; 2:213-218.
-
(1996)
Mol Hum Reprod
, vol.2
, pp. 213-218
-
-
Ray, P.F.1
Handyside, A.H.2
-
102
-
-
0025764491
-
Using pcr in preimplantation genetic disease diagnosis
-
Navidi W, Arnheim N. Using PCR in preimplantation genetic disease diagnosis. Hum Reprod 1991; 6:836-849.
-
(1991)
Hum Reprod
, vol.6
, pp. 836-849
-
-
Navidi, W.1
Arnheim, N.2
-
103
-
-
0025292815
-
Preconception genetic diagnosis of cystic fibrosis. [letter]
-
Strom CM, Verlinsky Y, Milayeva S, Evsikov S, Cieslak J, Lifchez A, Valle J, Moise J, Ginsberg N, Applebaum M. Preconception genetic diagnosis of cystic fibrosis. [Letter]. Lancet 1990; 336:306-307.
-
(1990)
Lancet
, vol.336
, pp. 306-307
-
-
Strom, C.M.1
Verlinsky, Y.2
Milayeva, S.3
Evsikov, S.4
Cieslak, J.5
Lifchez, A.6
Valle, J.7
Moise, J.8
Ginsberg, N.9
Applebaum, M.10
-
104
-
-
0027964833
-
Reliability of polymerase chain reaction (Pcr) analysis of single cells for preimplantation genetic diagnosis
-
Strom CM, Rechitsky S, Wolf G, Verlinsky Y. Reliability of polymerase chain reaction (PCR) analysis of single cells for preimplantation genetic diagnosis. J Assist Reprod Genet 1994; 11:55-62.
-
(1994)
J Assist Reprod Genet
, vol.11
, pp. 55-62
-
-
Strom, C.M.1
Rechitsky, S.2
Wolf, G.3
Verlinsky, Y.4
-
105
-
-
0028021177
-
Preimplantation diagnosis of cystic fibrosis by simultaneous detection of the w1282x and delta f508 mutations
-
Avner R, Laufer N, Safran A, Kerem BS, Friedmann A, Mitrani Rosenbaum S. Preimplantation diagnosis of cystic fibrosis by simultaneous detection of the W1282X and delta F508 mutations. Hum Reprod 1994; 9:1676-1680.
-
(1994)
Hum Reprod
, vol.9
, pp. 1676-1680
-
-
Avner, R.1
Laufer, N.2
Safran, A.3
Kerem, B.S.4
Friedmann, A.5
Mitrani Rosenbaum, S.6
-
106
-
-
10144243496
-
Elimination of allele dropout (Ado) in single cell analysis for diagnosis of cystic fibrosis (cf) (abstract)
-
Ray PF, Winston RML, Handyside AH. Elimination of allele dropout (ADO) in single cell analysis for diagnosis of cystic fibrosis (CF) (abstract). Hum Reprod 1995; 10:64.
-
(1995)
Hum Reprod
, vol.10
, pp. 64
-
-
Ray, P.F.1
Winston, R.2
Handyside, A.H.3
-
107
-
-
0031902604
-
Allele dropout in polar bodies and blastomeres
-
Rechitsky S, Strom C, Verlinsky O, Amet T, Ivakhnenko V, Kukha-renko V, Kuliev A, Verlinsky Y. Allele dropout in polar bodies and blastomeres. J Assist Reprod Genet 1998; 15:253-257.
-
(1998)
J Assist Reprod Genet
, vol.15
, pp. 253-257
-
-
Rechitsky, S.1
Strom, C.2
Verlinsky, O.3
Amet, T.4
Ivakhnenko, V.5
Kukha-Renko, V.6
Kuliev, A.7
Verlinsky, Y.8
-
108
-
-
0029061813
-
Simultaneous dna ‘fingerprinting,’ diagnosis of sex and singlegene defect status from single cells
-
Findlay I, Urquhart A, Quirke P, Sullivan K, Rutherford AJ, Lilford RJ. Simultaneous DNA ‘fingerprinting,’ diagnosis of sex and singlegene defect status from single cells. Hum Reprod 1995; 10:1005-1013.
-
(1995)
Hum Reprod
, vol.10
, pp. 1005-1013
-
-
Findlay, I.1
Urquhart, A.2
Quirke, P.3
Sullivan, K.4
Rutherford, A.J.5
Lilford, R.J.6
-
109
-
-
0032902433
-
Preimplantation genetic diagnosis using fluorescent polymerase chain reaction: Results and future developments
-
Findlay I, Matthews P, Quirke P. Preimplantation genetic diagnosis using fluorescent polymerase chain reaction: results and future developments. J Assist Reprod Genet 1999; 16:199-206.
-
(1999)
J Assist Reprod Genet
, vol.16
, pp. 199-206
-
-
Findlay, I.1
Matthews, P.2
Quirke, P.3
-
110
-
-
0029124756
-
Marfan syndrome as a paradigm for transcript-targeted preimplantation diagnosis of heterozygous mutations
-
Eldadah ZA, Grifo JA, Dietz HC. Marfan syndrome as a paradigm for transcript-targeted preimplantation diagnosis of heterozygous mutations. Nat Med 1995; 1:798-803.
-
(1995)
Nat Med
, vol.1
, pp. 798-803
-
-
Eldadah, Z.A.1
Grifo, J.A.2
Dietz, H.C.3
-
111
-
-
0030830374
-
Paternal transcripts for glucose-6-phosphate dehydrogenase and adenosine deaminase are first detectable in the human preimplantation embryo at the three- to four-cell stage
-
Taylor DM, Ray PF, Ao A, Winston RM, Handyside AH. Paternal transcripts for glucose-6-phosphate dehydrogenase and adenosine deaminase are first detectable in the human preimplantation embryo at the three- to four-cell stage. Mol Reprod Dev 1997; 48:442-448.
-
(1997)
Mol Reprod Dev
, vol.48
, pp. 442-448
-
-
Taylor, D.M.1
Ray, P.F.2
Ao, A.3
Winston, R.M.4
Handyside, A.H.5
-
112
-
-
0344731402
-
First unaffected pregnancy using preimplantation genetic diagnosis for sickle cell anemia
-
Xu K, Shi ZM, Veeck LL, Hughes MR, Rosenwaks Z. First unaffected pregnancy using preimplantation genetic diagnosis for sickle cell anemia. JAMA 1999; 281:1701-1706.
-
(1999)
JAMA
, vol.281
, pp. 1701-1706
-
-
Xu, K.1
Shi, Z.M.2
Veeck, L.L.3
Hughes, M.R.4
Rosenwaks, Z.5
-
113
-
-
0032980524
-
Fluorescent pcr and automated fragment analysis in preimplantation genetic diagnosis for 21-hydroxylase deficiency in congenital adrenal hyperplasia
-
Van de Velde H, Sermon K, De Vos A, Lissens W, Joris H, Vandervorst M, Van Steirteghem A, Liebaers I. Fluorescent PCR and automated fragment analysis in preimplantation genetic diagnosis for 21-hydroxylase deficiency in congenital adrenal hyperplasia. Mol Hum Reprod 1999; 5:691-696.
-
(1999)
Mol Hum Reprod
, vol.5
, pp. 691-696
-
-
Van De Velde, H.1
Sermon, K.2
De Vos, A.3
Lissens, W.4
Joris, H.5
Vandervorst, M.6
Van Steirteghem, A.7
Liebaers, I.8
-
114
-
-
0028906241
-
Preimplantation genetic diagnosis for tay-sachs disease: Successful pregnancy after pre-embryo biopsy and gene amplification by polymerase chain reaction
-
Gibbons WE, Gitlin SA, Lanzendorf SE, Kaufmann RA, Slotnick RN, Hodgen GD. Preimplantation genetic diagnosis for Tay-Sachs disease: successful pregnancy after pre-embryo biopsy and gene amplification by polymerase chain reaction. Fertil Steril 1995; 63:723-728.
-
(1995)
Fertil Steril
, vol.63
, pp. 723-728
-
-
Gibbons, W.E.1
Gitlin, S.A.2
Lanzendorf, S.E.3
Kaufmann, R.A.4
Slotnick, R.N.5
Hodgen, G.D.6
-
115
-
-
7844248269
-
Pregnancy after preimplantation genetic diagnosis for charcot-marie-tooth disease type 1a
-
De Vos A, Sermon K, Van de Velde H, Joris H, Vandervorst M, Lissens W, Mortier G, De Sutter P, Lofgren A, Van Broeckhoven C, Liebaers I, Van Steirteghem A. Pregnancy after preimplantation genetic diagnosis for Charcot-Marie-Tooth disease type 1A. Mol Hum Reprod 1998; 4:978-984.
-
(1998)
Mol Hum Reprod
, vol.4
, pp. 978-984
-
-
De Vos, A.1
Sermon, K.2
Van De Velde, H.3
Joris, H.4
Vandervorst, M.5
Lissens, W.6
Mortier, G.7
De Sutter, P.8
Lofgren, A.9
Van Broeckhoven, C.10
Liebaers, I.11
Van Steirteghem, A.12
-
116
-
-
0033917588
-
Two pregnancies after preimplantation genetic diagnosis for osteogenesis imperfecta type i and type iv
-
De Vos A, Sermon K, Van de Velde H, Joris H, Vandervorst M, Lissens W, De Paepe A, Liebaers I, Van Steirteghem A. Two pregnancies after preimplantation genetic diagnosis for osteogenesis imperfecta type I and type IV. Hum Genet 2000; 106:605-613.
-
(2000)
Hum Genet
, vol.106
, pp. 605-613
-
-
De Vos, A.1
Sermon, K.2
Van De Velde, H.3
Joris, H.4
Vandervorst, M.5
Lissens, W.6
De Paepe, A.7
Liebaers, I.8
Van Steirteghem, A.9
-
117
-
-
85006324393
-
Preimplantation diagnosis for p52 tumour suppressor gene mutations
-
Verlinsky Y, Rechitsky S, Verlinsky O, Xu K, Schattman G, Mascian-gelo C, Ginberg N, Strom C, Rosenwaks Z, Kuliev A. Preimplantation diagnosis for p52 tumour suppressor gene mutations. Reprod Biomed Online 2001; 2:102-105.
-
(2001)
Reprod Biomed Online
, vol.2
, pp. 102-105
-
-
Verlinsky, Y.1
Rechitsky, S.2
Verlinsky, O.3
Xu, K.4
Schattman, G.5
Mascian-Gelo, C.6
Ginberg, N.7
Strom, C.8
Rosenwaks, Z.9
Kuliev, A.10
-
118
-
-
0031971471
-
Preimplantation diagnosis of autosomal dominant retinitis pigmentosum using two simultaneous single cell assays for a point mutation in the rhodopsin gene
-
Strom CM, Rechitsky S, Wolf G, Cieslak J, Kuliev A, Verlinsky Y. Preimplantation diagnosis of autosomal dominant retinitis pigmentosum using two simultaneous single cell assays for a point mutation in the rhodopsin gene. Mol Hum Reprod 1998; 4:351-355.
-
(1998)
Mol Hum Reprod
, vol.4
, pp. 351-355
-
-
Strom, C.M.1
Rechitsky, S.2
Wolf, G.3
Cieslak, J.4
Kuliev, A.5
Verlinsky, Y.6
-
119
-
-
0031959726
-
Preimplantation diagnosis of non-deletion duchenne muscular dystrophy (Dmd) by linkage polymerase chain reaction analysis
-
Lee SH, Kwak IP, Cha KE, Park SE, Kim NK, Cha KY. Preimplantation diagnosis of non-deletion Duchenne muscular dystrophy (DMD) by linkage polymerase chain reaction analysis. Mol Hum Reprod 1998; 4:345-349.
-
(1998)
Mol Hum Reprod
, vol.4
, pp. 345-349
-
-
Lee, S.H.1
Kwak, I.P.2
Cha, K.E.3
Park, S.E.4
Kim, N.K.5
Cha, K.Y.6
|