-
1
-
-
0036899740
-
Preimplantation genetic diagnosis using FISH for carriers of Robertsonian translocations; The Portuguese experience
-
Alves C, Sousa M, Silva J, Barros A. 2002. Preimplantation genetic diagnosis using FISH for carriers of Robertsonian translocations; The Portuguese experience. Prenat Diag 22:1153-1162.
-
(2002)
Prenat Diag
, vol.22
, pp. 1153-1162
-
-
Alves, C.1
Sousa, M.2
Silva, J.3
Barros, A.4
-
2
-
-
3042550513
-
Sperm FISH studies in seven male carriers of Robertsonian translocation t(13;14)(q10;q11)
-
Anton E, Blanco J, Egozcue J, Vidal F. 2004. Sperm FISH studies in seven male carriers of Robertsonian translocation t(13;14)(q10;q11). Hum Reprod 19:1345-1351.
-
(2004)
Hum Reprod
, vol.19
, pp. 1345-1351
-
-
Anton, E.1
Blanco, J.2
Egozcue, J.3
Vidal, F.4
-
3
-
-
47149096761
-
Repeated fetal loss in two related first cousins marriages with couples all carrying the same translocation t(13q;14q)
-
Bahçe M, Oõur G, Ymirzalyoõlu N, Gümüp H, Kervancyoölu O, Özen S, Baltacy V, Vamos E. 1996. Repeated fetal loss in two related first cousins marriages with couples all carrying the same translocation t(13q;14q). Eur J Hum Genet 4 (Suppl l):35-36.
-
(1996)
Eur J Hum Genet
, vol.4
, Issue.SUPPL. L
, pp. 35-36
-
-
Bahçe, M.1
Oõur, G.2
Ymirzalyoõlu, N.3
Gümüp, H.4
Kervancyoölu, O.5
Özen, S.6
Baltacy, V.7
Vamos, E.8
-
4
-
-
0033840894
-
Improvements of preimplantation diagnosis of aneuploidy by using microwave-hybridization, cell recycling and monocolor labeling of probes
-
Bahçe M, Escudero T, Sanadalinas M, Morrison L, Legator M, Munné S. 2000. Improvements of preimplantation diagnosis of aneuploidy by using microwave-hybridization, cell recycling and monocolor labeling of probes. Mol Hum Reprod 9:849-854.
-
(2000)
Mol Hum Reprod
, vol.9
, pp. 849-854
-
-
Bahçe, M.1
Escudero, T.2
Sanadalinas, M.3
Morrison, L.4
Legator, M.5
Munné, S.6
-
5
-
-
0027202605
-
A complex chromosomal rearrangement detected prenatally and studied by fluorescent in situ hybridization
-
Batista DAS, Tuck-Muller CM, Martinez JE, Kearns WG, Pearson PL, Steffen G 1993. A complex chromosomal rearrangement detected prenatally and studied by fluorescent in situ hybridization. Hum Genet 92:117-121.
-
(1993)
Hum Genet
, vol.92
, pp. 117-121
-
-
Batista, D.A.S.1
Tuck-Muller, C.M.2
Martinez, J.E.3
Kearns, W.G.4
Pearson, P.L.5
Steffen, G.6
-
6
-
-
26244468341
-
Segregation of chromosomes in sperm of reciprocal translocation carriers: A review
-
Benet J, Oliver-Bonet M, Cifuentes P, Templado C, Navarro J. 2005. Segregation of chromosomes in sperm of reciprocal translocation carriers: A review. Cytogenet Genome Res 111:281-290.
-
(2005)
Cytogenet Genome Res
, vol.111
, pp. 281-290
-
-
Benet, J.1
Oliver-Bonet, M.2
Cifuentes, P.3
Templado, C.4
Navarro, J.5
-
7
-
-
0037093698
-
Familial complex chromosomal rearrangement resulting in a recombinant chromosome
-
Berend SA, Bodamer OAF, Shapira SK, Shaffer LG, Bacino CA. 2002. Familial complex chromosomal rearrangement resulting in a recombinant chromosome. Am J Med Genet 109:311-317.
-
(2002)
Am J Med Genet
, vol.109
, pp. 311-317
-
-
Berend, S.A.1
Bodamer, O.A.F.2
Shapira, S.K.3
Shaffer, L.G.4
Bacino, C.A.5
-
8
-
-
0023911391
-
Are double translocations double trouble?
-
Bowser-Riley SM, Griffiths MJ, Creasy MR, Farndon PA, Martin KE, Thomson DAG, Larkins SA, Johnson RA, Watt JL. 1988. Are double translocations double trouble? J Med Genet 25:209-213.
-
(1988)
J Med Genet
, vol.25
, pp. 209-213
-
-
Bowser-Riley, S.M.1
Griffiths, M.J.2
Creasy, M.R.3
Farndon, P.A.4
Martin, K.E.5
Thomson, D.A.G.6
Larkins, S.A.7
Johnson, R.A.8
Watt, J.L.9
-
9
-
-
0032408211
-
Sperm segregation analysis of a complex rearrangement, 2;22;11, by whole chromosome painting
-
Cifuentes P, Navarro J, Míguez L, Egozcue J, Benet J. 1998. Sperm segregation analysis of a complex rearrangement, 2;22;11, by whole chromosome painting. Cytogenet Cell Genet 82:204-209.
-
(1998)
Cytogenet Cell Genet
, vol.82
, pp. 204-209
-
-
Cifuentes, P.1
Navarro, J.2
Míguez, L.3
Egozcue, J.4
Benet, J.5
-
10
-
-
0033941370
-
Analysis of chromosome abnormalities in sperm and embryos from two 45,XY,t(13;14)(q10;q10)
-
Escudero T, Lee M, Carrel D, Blanco J, Munné S. 2000. Analysis of chromosome abnormalities in sperm and embryos from two 45,XY,t(13;14)(q10;q10). Prenat Diag 20:599-602.
-
(2000)
Prenat Diag
, vol.20
, pp. 599-602
-
-
Escudero, T.1
Lee, M.2
Carrel, D.3
Blanco, J.4
Munné, S.5
-
11
-
-
0034805033
-
Preimplantation genetic diagnosis of pericentric inversions
-
Escudero T, Lee M, Stevens J, Sandalinas M, Munné S. 2001. Preimplantation genetic diagnosis of pericentric inversions. Prenat Diagn 21:760-766.
-
(2001)
Prenat Diagn
, vol.21
, pp. 760-766
-
-
Escudero, T.1
Lee, M.2
Stevens, J.3
Sandalinas, M.4
Munné, S.5
-
12
-
-
0037497360
-
Predictive value of sperm chromosome analysis on the putcome of PGD for translocations
-
Escudero T, Abdelhadi I, Sandalinas M, Munné S. 2003. Predictive value of sperm chromosome analysis on the putcome of PGD for translocations. Fertil Steril 79 (Suppl 3):1528-1534.
-
(2003)
Fertil Steril
, vol.79
, Issue.SUPPL. 3
, pp. 1528-1534
-
-
Escudero, T.1
Abdelhadi, I.2
Sandalinas, M.3
Munné, S.4
-
13
-
-
0027472131
-
Meiotic analysis by FISH of a human male, 46,XY,t(15;20)(qll.2;qll.2) translocation heterozygote: Quadrivalent configuration, orientation and first meiotic segregation
-
Goldman ASH, Hulten MA. 1993. Meiotic analysis by FISH of a human male, 46,XY,t(15;20)(qll.2;qll.2) translocation heterozygote: Quadrivalent configuration, orientation and first meiotic segregation. Chromosoma 102:102-111.
-
(1993)
Chromosoma
, vol.102
, pp. 102-111
-
-
Goldman, A.S.H.1
Hulten, M.A.2
-
14
-
-
0023853716
-
Reproductive risks for carriers of complex chromosome rearrangements: Analysis of 25 families
-
Gorski JL, Kistenmacher ML, Punnett HH, Zackai EH, Emanuel BS. 1988. Reproductive risks for carriers of complex chromosome rearrangements: Analysis of 25 families. Am J Med Genet 29:247-261.
-
(1988)
Am J Med Genet
, vol.29
, pp. 247-261
-
-
Gorski, J.L.1
Kistenmacher, M.L.2
Punnett, H.H.3
Zackai, E.H.4
Emanuel, B.S.5
-
16
-
-
0031826303
-
Preimplantation genetic diagnosis of a large pericentric inversion of chromosome 5
-
Iwarsson E, Ährlund-Richter L, Inzunza J, Rosenlund B, Fridström M, Hillensjö T, Sjöblom P, Nordenskjöld M, Blennow E. 1998. Preimplantation genetic diagnosis of a large pericentric inversion of chromosome 5. Molec Hum Reprod 4:719-723.
-
(1998)
Molec Hum Reprod
, vol.4
, pp. 719-723
-
-
Iwarsson, E.1
Ährlund-Richter, L.2
Inzunza, J.3
Rosenlund, B.4
Fridström, M.5
Hillensjö, T.6
Sjöblom, P.7
Nordenskjöld, M.8
Blennow, E.9
-
17
-
-
4043154186
-
Efficacy and clinical outcome of preimplantation genetic diagnosis using FISH for couples of reciprocal and Robertsonian translocations: The Korean experience
-
Lim CK, Jun JH, Min DM, Lee H-S, Kim JY, Koong MK, Kang IS. 2004. Efficacy and clinical outcome of preimplantation genetic diagnosis using FISH for couples of reciprocal and Robertsonian translocations: The Korean experience. Prenat Diag 24:556-561.
-
(2004)
Prenat Diag
, vol.24
, pp. 556-561
-
-
Lim, C.K.1
Jun, J.H.2
Min, D.M.3
Lee, H.-S.4
Kim, J.Y.5
Koong, M.K.6
Kang, I.S.7
-
18
-
-
0030906960
-
Recombination in a balanced translocation of a mother leading to a balanced reciprocal translocation in the child. Review of 60 cases of balanced complex translocations
-
Madan K, Nieuwint AWM, van Bever Y. 1997. Recombination in a balanced translocation of a mother leading to a balanced reciprocal translocation in the child. Review of 60 cases of balanced complex translocations. Hum Genet 99:806-815.
-
(1997)
Hum Genet
, vol.99
, pp. 806-815
-
-
Madan, K.1
Nieuwint, A.W.M.2
van Bever, Y.3
-
19
-
-
0028118866
-
Analysis of sperm chromosome complements from a man heterozygous for a pericentric inversion of chromosome 1
-
Martin RH, Chernos JE, Lowry RB, Pattison HA, Barclay L, Ko E. 1994. Analysis of sperm chromosome complements from a man heterozygous for a pericentric inversion of chromosome 1. Hum Genet 93:135-138.
-
(1994)
Hum Genet
, vol.93
, pp. 135-138
-
-
Martin, R.H.1
Chernos, J.E.2
Lowry, R.B.3
Pattison, H.A.4
Barclay, L.5
Ko, E.6
-
20
-
-
0021743056
-
Homozygosity for a Robertsonian translocation (13q14) in three offspring of heterozygous parents
-
Martinez-Castro P, Ramos MC, Rey JA, Benitez J, Sanchez-Cascos A. 1984. Homozygosity for a Robertsonian translocation (13q14) in three offspring of heterozygous parents. Cytogenet Cell Genet 38:310-312.
-
(1984)
Cytogenet Cell Genet
, vol.38
, pp. 310-312
-
-
Martinez-Castro, P.1
Ramos, M.C.2
Rey, J.A.3
Benitez, J.4
Sanchez-Cascos, A.5
-
21
-
-
0031943492
-
Chromosome abnormalities in 447 couples undergoing intracytoplasmic sperm injection-prevalence, types, sex distribution and reproductive relevance
-
Meschede D, Lemcke B, Exeler J, De Geyter C, Behre HM, Nieschlag E, Horst J. 1998. Chromosome abnormalities in 447 couples undergoing intracytoplasmic sperm injection-prevalence, types, sex distribution and reproductive relevance. Hum Reprod 13:576-582.
-
(1998)
Hum Reprod
, vol.13
, pp. 576-582
-
-
Meschede, D.1
Lemcke, B.2
Exeler, J.3
De Geyter, C.4
Behre, H.M.5
Nieschlag, E.6
Horst, J.7
-
22
-
-
0036490364
-
Preimplantation genetic diagnosis of numerical and structural chromosome abnormalities
-
Munné S. 2002. Preimplantation genetic diagnosis of numerical and structural chromosome abnormalities. Reprod BioMed Onl 4:183-196.
-
(2002)
Reprod BioMed Onl
, vol.4
, pp. 183-196
-
-
Munné, S.1
-
23
-
-
26244433893
-
Analysis of chromosome segregation during preimplantation genetic diagnosis in both male and female translocation heterozygotes
-
Munné S. 2005. Analysis of chromosome segregation during preimplantation genetic diagnosis in both male and female translocation heterozygotes. Cytogenet Genome Res 111:305-309.
-
(2005)
Cytogenet Genome Res
, vol.111
, pp. 305-309
-
-
Munné, S.1
-
24
-
-
0031879163
-
Preimplantation genetic analysis of translocations: Case-specific probes for interphase cell analysis
-
Munné S, Fung J, Cassel MJ, Marquez C, Weier HUG. 1998a. Preimplantation genetic analysis of translocations: case-specific probes for interphase cell analysis. Hum Genet 102:663-674.
-
(1998)
Hum Genet
, vol.102
, pp. 663-674
-
-
Munné, S.1
Fung, J.2
Cassel, M.J.3
Marquez, C.4
Weier, H.U.G.5
-
25
-
-
0031977265
-
First pregnancies after preconception diagnosis of translocations of maternal origin
-
Munné S, Scott R, Sable D, Cohen J. 1998b. First pregnancies after preconception diagnosis of translocations of maternal origin. Fertil Steril 69:675-681.
-
(1998)
Fertil Steril
, vol.69
, pp. 675-681
-
-
Munné, S.1
Scott, R.2
Sable, D.3
Cohen, J.4
-
26
-
-
7144262414
-
Spontaneous abortions are reduced after preconception diagnosis of translocations
-
Munné S, Morrison L, Fung J, Marquez C, Weier U, Bahçe M, Sable D, Grundfeld L, Schoolcraft B, Scott R, Cohen J. 1998c. Spontaneous abortions are reduced after preconception diagnosis of translocations. J Assis Reprod Genet 15:290-296.
-
(1998)
J Assis Reprod Genet
, vol.15
, pp. 290-296
-
-
Munné, S.1
Morrison, L.2
Fung, J.3
Marquez, C.4
Weier, U.5
Bahçe, M.6
Sable, D.7
Grundfeld, L.8
Schoolcraft, B.9
Scott, R.10
Cohen, J.11
-
27
-
-
0034075712
-
Outcome of preimplantation genetic diagnosis of translocations
-
Munné S, Sandalinas M, Escudero T, Fung J, Gianaroli L, Cohen J. 2000. Outcome of preimplantation genetic diagnosis of translocations. Fertil Steril 73:1209-1218.
-
(2000)
Fertil Steril
, vol.73
, pp. 1209-1218
-
-
Munné, S.1
Sandalinas, M.2
Escudero, T.3
Fung, J.4
Gianaroli, L.5
Cohen, J.6
-
28
-
-
19944414333
-
Predictability of preimplantation genetic diagnosis of aneuploidy and translocations on prospective attempts
-
Munné S, Escudero T, Pere C, Xuezhong Z, Oter M, Garrisi M, Barnes F, Zouves C, Werlin L, Magli C, Cohen J. 2004. Predictability of preimplantation genetic diagnosis of aneuploidy and translocations on prospective attempts. Reprod Biomed Online 9:645-651.
-
(2004)
Reprod Biomed Online
, vol.9
, pp. 645-651
-
-
Munné, S.1
Escudero, T.2
Pere, C.3
Xuezhong, Z.4
Oter, M.5
Garrisi, M.6
Barnes, F.7
Zouves, C.8
Werlin, L.9
Magli, C.10
Cohen, J.11
-
29
-
-
14944366531
-
Negligible interchromosomal effect in embryos of Robertsonian translocation carriers
-
Munné S, Escudero T, Fischer J, Chen S, Hill J, Stelling JR, Estop E. 2005. Negligible interchromosomal effect in embryos of Robertsonian translocation carriers. Reprod Biomed Online 10:363-369.
-
(2005)
Reprod Biomed Online
, vol.10
, pp. 363-369
-
-
Munné, S.1
Escudero, T.2
Fischer, J.3
Chen, S.4
Hill, J.5
Stelling, J.R.6
Estop, E.7
-
31
-
-
4444331256
-
Flourescence in situ hybridization characterization of apparently balanced translocation reveals cryptic complex chromosomal rearrangements with unexpected level of complexity
-
Patsalis PC, Evangelidou P, Charalambous S, Sismani C. 2004. Flourescence in situ hybridization characterization of apparently balanced translocation reveals cryptic complex chromosomal rearrangements with unexpected level of complexity. Eur J Hum Genet 12:647-653.
-
(2004)
Eur J Hum Genet
, vol.12
, pp. 647-653
-
-
Patsalis, P.C.1
Evangelidou, P.2
Charalambous, S.3
Sismani, C.4
-
32
-
-
26244453150
-
Segregation of chromosomes in sperm of Robertsonian translocation carriers
-
Roux C, Tripogney C, Morel F, Joanne C, Fellmann F, Clavequin MC, Bresson JL. 2005. Segregation of chromosomes in sperm of Robertsonian translocation carriers. Cytogenet Genome Res 111:291-296.
-
(2005)
Cytogenet Genome Res
, vol.111
, pp. 291-296
-
-
Roux, C.1
Tripogney, C.2
Morel, F.3
Joanne, C.4
Fellmann, F.5
Clavequin, M.C.6
Bresson, J.L.7
-
33
-
-
0022345930
-
A complex three breakpoint translocation involving chromosomes 2,4 and 9 identified by meiotic investigations of a human male ascertained for subfertility
-
Saadallah N, Hulten M. 1985. A complex three breakpoint translocation involving chromosomes 2,4 and 9 identified by meiotic investigations of a human male ascertained for subfertility. Hum Genet 71:312-320.
-
(1985)
Hum Genet
, vol.71
, pp. 312-320
-
-
Saadallah, N.1
Hulten, M.2
-
34
-
-
0035157468
-
Robertsonian translocations-reproductive risks and indications for preimplantation genetic diagnosis
-
Scriven PN, Flinter FA, Braude PR, Mackie Oglivie C. 2001. Robertsonian translocations-reproductive risks and indications for preimplantation genetic diagnosis. Hum Reprod 16:2267-2273.
-
(2001)
Hum Reprod
, vol.16
, pp. 2267-2273
-
-
Scriven, P.N.1
Flinter, F.A.2
Braude, P.R.3
Mackie Oglivie, C.4
-
35
-
-
0032780568
-
Chromosome translocations in couples with in vitro fertilization implantation failure
-
Stern C, Pertile M, Norris H, Hale L, Baker HWG. 1999. Chromosome translocations in couples with in vitro fertilization implantation failure. Hum Reprod 14:2097-2101.
-
(1999)
Hum Reprod
, vol.14
, pp. 2097-2101
-
-
Stern, C.1
Pertile, M.2
Norris, H.3
Hale, L.4
Baker, H.W.G.5
-
36
-
-
0030469647
-
Intracytoplasmic sperm injection in infertile patients with structural chromosome abnormalities
-
Testart J, Gautier E, Brami C, Rolet F, Sedbon E, Thebault A. 1996. Intracytoplasmic sperm injection in infertile patients with structural chromosome abnormalities. Hum Reprod 11:2609-2612.
-
(1996)
Hum Reprod
, vol.11
, pp. 2609-2612
-
-
Testart, J.1
Gautier, E.2
Brami, C.3
Rolet, F.4
Sedbon, E.5
Thebault, A.6
-
37
-
-
0031909539
-
Increased frequency of congenital chromosomal aberrations in female partners of couples undergoing intracytoplasmic sperm injection
-
Van der Ven K, Peschka B, Montag M, Lange R, Schwanitz G, Van der Ven HH. 1998. Increased frequency of congenital chromosomal aberrations in female partners of couples undergoing intracytoplasmic sperm injection. Hum Reprod 13:48-54.
-
(1998)
Hum Reprod
, vol.13
, pp. 48-54
-
-
Van der Ven, K.1
Peschka, B.2
Montag, M.3
Lange, R.4
Schwanitz, G.5
Van der Ven, H.H.6
-
38
-
-
0032902635
-
Karyotyping of human oocytes by chromosomal analysis of the second polar body
-
Verlinsky Y, Evsikov S. 1999. Karyotyping of human oocytes by chromosomal analysis of the second polar body. Molec Human Reprod 5:89-95.
-
(1999)
Molec Human Reprod
, vol.5
, pp. 89-95
-
-
Verlinsky, Y.1
Evsikov, S.2
-
39
-
-
23144438542
-
Preimplantation testing for chromosomal disorders improves reproductive outcome of poor-prognosis patients
-
Verlinsky Y, Tur-Kaspa I, Cieslak J, Bernal A, Morris R, Taranissi M, Kaplan B, Kuliev A. 2005. Preimplantation testing for chromosomal disorders improves reproductive outcome of poor-prognosis patients. Reprod Biomed Online 11:219-225.
-
(2005)
Reprod Biomed Online
, vol.11
, pp. 219-225
-
-
Verlinsky, Y.1
Tur-Kaspa, I.2
Cieslak, J.3
Bernal, A.4
Morris, R.5
Taranissi, M.6
Kaplan, B.7
Kuliev, A.8
-
40
-
-
0036835854
-
Nuclear transfer for full karyotyping and preimplantation diagnosis for translocations
-
Verlinsky Y, Cieslak V, Esviskov G, Galat V, Kuliev A. 2002. Nuclear transfer for full karyotyping and preimplantation diagnosis for translocations. Reprod Biomed Online 5:300-305.
-
(2002)
Reprod Biomed Online
, vol.5
, pp. 300-305
-
-
Verlinsky, Y.1
Cieslak, V.2
Esviskov, G.3
Galat, V.4
Kuliev, A.5
-
41
-
-
0033021910
-
Rapid visualization of metaphase chromosomes in single human blastomeres after fusion with in vitro matured bovine eggs
-
Willadsen S, Levron J, Munné S, Schimmel T, Márquez C, Scott R, Cohen J. 1999. Rapid visualization of metaphase chromosomes in single human blastomeres after fusion with in vitro matured bovine eggs. Human Reprod 2:470-475.
-
(1999)
Human Reprod
, vol.2
, pp. 470-475
-
-
Willadsen, S.1
Levron, J.2
Munné, S.3
Schimmel, T.4
Márquez, C.5
Scott, R.6
Cohen, J.7
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