-
1
-
-
0002418993
-
The frequency of chromosome abnormalities detected in consecutive newborn studies - Differences between studies - Results by sex and by severity of phenotypic involvement
-
Hook EB, Porter LH (eds): New York: Academic Press
-
Hook EB, Hamerton JL: The frequency of chromosome abnormalities detected in consecutive newborn studies - differences between studies - results by sex and by severity of phenotypic involvement.; in Hook EB, Porter LH (eds): Population Cytogenetics. New York: Academic Press, 1977; pp 66-79.
-
(1977)
Population Cytogenetics
, pp. 66-79
-
-
Hook, E.B.1
Hamerton, J.L.2
-
2
-
-
0032425535
-
Chromosome translocations: Segregation modes and strategies for preimplantation genetic diagnosis
-
Scriven PN, Handyside AH, Mackie Ogilvie C: Chromosome translocations: segregation modes and strategies for preimplantation genetic diagnosis. Prenat Diag 1998; 18: 1437-1449.
-
(1998)
Prenat. Diag.
, vol.18
, pp. 1437-1449
-
-
Scriven, P.N.1
Handyside, A.H.2
Mackie Ogilvie, C.3
-
4
-
-
0018953638
-
Reciprocal translocations: A way to predict the mode of imbalanced segregation by pachytene-diagram drawing
-
Jalbert P, Sele B, Jalbert H: Reciprocal translocations: a way to predict the mode of imbalanced segregation by pachytene-diagram drawing. Hum Genet 1980; 55: 209-222.
-
(1980)
Hum. Genet.
, vol.55
, pp. 209-222
-
-
Jalbert, P.1
Sele, B.2
Jalbert, H.3
-
5
-
-
0003263102
-
Types of imbalances in human reciprocal translocations: Risks at birth
-
Daniel A (ed): New York: Alan R. Liss, Inc
-
Jalbert P, Jalbert H, Sele B: Types of imbalances in human reciprocal translocations: risks at birth; in: Daniel A (ed): The Cytogenetics of Mammalian Autosomal Rearrangements. New York: Alan R. Liss, Inc., 1988, pp 267-291.
-
(1988)
The Cytogenetics of Mammalian Autosomal Rearrangements
, pp. 267-291
-
-
Jalbert, P.1
Jalbert, H.2
Sele, B.3
-
6
-
-
0033849378
-
Meiotic studies of a human male carrier of the common translocation, t(11;22), suggests postzygotic selection rather than preferential 3:1 M1 segregation as the cause of liveborn offspring with an unbalanced translocation
-
Armstrong SJ, Goldman ASH, Speed RM, Hulten MA: meiotic studies of a human male carrier of the common translocation, t(11;22), suggests postzygotic selection rather than preferential 3:1 M1 segregation as the cause of liveborn offspring with an unbalanced translocation. Am J Hum Genet 2000; 67: 601-609.
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 601-609
-
-
Armstrong, S.J.1
Goldman, A.S.H.2
Speed, R.M.3
Hulten, M.A.4
-
7
-
-
0027472131
-
Meiotic analysis by FISH of a human male 46,XY,t(15;20)(q11.2q11.2) translocation heterozygote: Quadrivalent configuration, orientation, and first meiotic segregation
-
Goldman ASH, Hulten MA: Meiotic analysis by FISH of a human male 46,XY,t(15;20)(q11.2q11.2) translocation heterozygote: quadrivalent configuration, orientation, and first meiotic segregation. Chromosoma 1993; 102: 102-111.
-
(1993)
Chromosoma
, vol.102
, pp. 102-111
-
-
Goldman, A.S.H.1
Hulten, M.A.2
-
8
-
-
0027516966
-
Analysis of chiasma frequency and first meiotic segregation in a human male reciprocal translocation heterozygote, t(1;11)(p36.3;q13.1), using fluorescence in situ hybridisation
-
Goldman ASH, Hulten MA: Analysis of chiasma frequency and first meiotic segregation in a human male reciprocal translocation heterozygote, t(1;11)(p36.3;q13.1), using fluorescence in situ hybridisation. Cytogenet Cell Genet 1993; 63: 16-23.
-
(1993)
Cytogenet. Cell Genet.
, vol.63
, pp. 16-23
-
-
Goldman, A.S.H.1
Hulten, M.A.2
-
9
-
-
0028946651
-
Segregation analysis of four translocations, t(2;18), t(3;15), t(5;7), and t(10,12), by sperm chromosome studies and a review of the literature
-
Estop AM, Van Kirk V, Ceiply K: Segregation analysis of four translocations, t(2;18), t(3;15), t(5;7), and t(10,12), by sperm chromosome studies and a review of the literature. Cytogenet Cell Genet 1995; 70: 60-67.
-
(1995)
Cytogenet. Cell Genet.
, vol.70
, pp. 60-67
-
-
Estop, A.M.1
Van Kirk, V.2
Ceiply, K.3
-
10
-
-
0028855742
-
Sperm chromosome complements in a man heterozygous for a reciprocal translocation 46,XY,t(9;13)(q21.1;q21.2) and a review of the literature
-
Martin RH, Spriggs EL: Sperm chromosome complements in a man heterozygous for a reciprocal translocation 46,XY,t(9;13)(q21.1;q21.2) and a review of the literature. Clin Genet 1995; 47: 42-46.
-
(1995)
Clin. Genet.
, vol.47
, pp. 42-46
-
-
Martin, R.H.1
Spriggs, E.L.2
-
11
-
-
0028869099
-
Meiotic segregation in males heterozygote for reciprocal translocation: Analysis of sperm nuclei by two and three colour fluorescence in situ hybridization
-
Rousseaux S, Chevret E, Moneil M et al: Meiotic segregation in males heterozygote for reciprocal translocation: analysis of sperm nuclei by two and three colour fluorescence in situ hybridization. Cytogenet Cell Genet 1995; 71: 240-246.
-
(1995)
Cytogenet. Cell Genet.
, vol.71
, pp. 240-246
-
-
Rousseaux, S.1
Chevret, E.2
Moneil, M.3
-
12
-
-
0030773488
-
Meiotic segregation, recombination, and gamete aneuploidy assessed in a t(1;10)(p22.1;q22.3) reciprocal translocation carrier by three-and four-probe multicolour FISH in sperm
-
Van Hummelen P, Manchester D, Lowe X, Wyrobek AJ: Meiotic segregation, recombination, and gamete aneuploidy assessed in a t(1;10)(p22.1;q22.3) reciprocal translocation carrier by three-and four-probe multicolour FISH in sperm. Am J Hum Genet 1997; 61: 651-659.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 651-659
-
-
Van Hummelen, P.1
Manchester, D.2
Lowe, X.3
Wyrobek, A.J.4
-
13
-
-
0030982686
-
The meiotic segregation pattern of a reciprocal translocation t(10;12)(q26.1;p13.3) by fluorescence in situ hybridization sperm analysis
-
Estop AM, Cieply KM, Aston CE: The meiotic segregation pattern of a reciprocal translocation t(10;12)(q26.1;p13.3) by fluorescence in situ hybridization sperm analysis. Eur J Hum Genet 1997; 5: 78-82.
-
(1997)
Eur. J. Hum. Genet.
, vol.5
, pp. 78-82
-
-
Estop, A.M.1
Cieply, K.M.2
Aston, C.E.3
-
14
-
-
0034967243
-
Meiotic segregation analysis in a t(4;8) carrier: Comparison of FISH methods on sperm chromosome metaphases and interphase sperm nuclei
-
Oliver-Bonet M, Navarro J, Codina-Pascual M, Carrera M, Egozcue J, Benet J: Meiotic segregation analysis in a t(4;8) carrier: comparison of FISH methods on sperm chromosome metaphases and interphase sperm nuclei. Eur J Hum Genet 2001; 9: 395-403.
-
(2001)
Eur. J. Hum. Genet.
, vol.9
, pp. 395-403
-
-
Oliver-Bonet, M.1
Navarro, J.2
Codina-Pascual, M.3
Carrera, M.4
Egozcue, J.5
Benet, J.6
-
15
-
-
0031788061
-
Meiotic segregation analysis by FISH investigations in sperm and spermatocytes of translocation heterozygotes
-
Armstrong SJ, Hulten MA: Meiotic segregation analysis by FISH investigations in sperm and spermatocytes of translocation heterozygotes. Eur J Hum Genet 1998; 6: 430-431.
-
(1998)
Eur. J. Hum. Genet.
, vol.6
, pp. 430-431
-
-
Armstrong, S.J.1
Hulten, M.A.2
-
16
-
-
0032962153
-
Immunocytogenetic detection of normal and abnormal oocytes in human fetal ovarian tissue in culture
-
Hartshorne GM, Barlow AL, Child TJ, Barlow DH, Hulten MA: Immunocytogenetic detection of normal and abnormal oocytes in human fetal ovarian tissue in culture. Hum Reprod 1999; 14: 172-182.
-
(1999)
Hum. Reprod.
, vol.14
, pp. 172-182
-
-
Hartshorne, G.M.1
Barlow, A.L.2
Child, T.J.3
Barlow, D.H.4
Hulten, M.A.5
-
17
-
-
0034030337
-
Female gamete segregation in two carriers of translocations involving 2q and 14q
-
Escudero T, Lee M, Sandalinas M, Munne S: Female gamete segregation in two carriers of translocations involving 2q and 14q. Prenat Diag 2000; 20: 235-237.
-
(2000)
Prenat. Diag.
, vol.20
, pp. 235-237
-
-
Escudero, T.1
Lee, M.2
Sandalinas, M.3
Munne, S.4
-
18
-
-
0034500988
-
Highly abnormal cleavage divisions in preimplantation embryos from translocation carriers
-
Iwarsson E, Malmgren H, Inzunza J et al: Highly abnormal cleavage divisions in preimplantation embryos from translocation carriers. Prenat Diag 2000; 20: 1038-1047.
-
(2000)
Prenat. Diag.
, vol.20
, pp. 1038-1047
-
-
Iwarsson, E.1
Malmgren, H.2
Inzunza, J.3
-
19
-
-
0034075712
-
Outcome of preimplantation genetic diagnosis of translocations
-
Munne S, Sandalinas M, Escudero T, Fung J, Gianaroli L, Cohen J: Outcome of preimplantation genetic diagnosis of translocations. Fertil Steril 2000; 73: 1209-1218.
-
(2000)
Fertil. Steril.
, vol.73
, pp. 1209-1218
-
-
Munne, S.1
Sandalinas, M.2
Escudero, T.3
Fung, J.4
Gianaroli, L.5
Cohen, J.6
-
20
-
-
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 C-T, Braude P, Mackie Ogilvie C: Clinical pregnancy following blastomere biopsy and PGD for a reciprocal translocation carrier: analysis of meiotic outcomes and embryo quality in two IVF cycles. Prenat Diag 2000; 20: 587-592.
-
(2000)
Prenat. Diag.
, vol.20
, pp. 587-592
-
-
Scriven, P.N.1
O'Mahony, F.2
Bickerstaff, H.3
Yeong, C.-T.4
Braude, P.5
Mackie Ogilvie, C.6
-
21
-
-
17944365343
-
PGD in female carriers of balanced Robertsonian and reciprocal translocations by first polar body analysis
-
Durban M, Benet J, Boada M et al: PGD in female carriers of balanced Robertsonian and reciprocal translocations by first polar body analysis. Hum Reprod Update 2001; 7: 591-602.
-
(2001)
Hum. Reprod. Update
, vol.7
, pp. 591-602
-
-
Durban, M.1
Benet, J.2
Boada, M.3
-
22
-
-
0003592020
-
ISCN: An international system for human cytogenetics nomenclature
-
Mitelman F (ed): Basel: S Karger
-
ISCN: An international system for human cytogenetics nomenclature; Mitelman F (ed): Basel: S Karger, 1995.
-
(1995)
-
-
-
23
-
-
0023874053
-
Human gene expression first occurs between the four-and eight-cell stages of preimplantation development
-
Braude PR, Bolton VN, Moore S: Human gene expression first occurs between the four-and eight-cell stages of preimplantation development. Nature 1988; 333: 459-461.
-
(1988)
Nature
, vol.333
, pp. 459-461
-
-
Braude, P.R.1
Bolton, V.N.2
Moore, S.3
-
24
-
-
0021344378
-
Analysis of human sperm chromosome complements from a male heterozygous for a reciprocal translocation t(11;22)(q23;q11)
-
Martin RH: Analysis of human sperm chromosome complements from a male heterozygous for a reciprocal translocation t(11;22)(q23;q11). Clin Genet 1984; 25: 357-361.
-
(1984)
Clin. Genet.
, vol.25
, pp. 357-361
-
-
Martin, R.H.1
-
25
-
-
0032994872
-
Multicolour fluorescence in situ hybridization analysis of the spermatazoa of a male heterozygous for a reciprocal translocation t(11;22)(q23;q11)
-
Estop AM, Cieply KM, Munne S, Feingold E: Multicolour fluorescence in situ hybridization analysis of the spermatazoa of a male heterozygous for a reciprocal translocation t(11;22)(q23;q11). Hum Genet 1999; 104: 412-417.
-
(1999)
Hum. Genet.
, vol.104
, pp. 412-417
-
-
Estop, A.M.1
Cieply, K.M.2
Munne, S.3
Feingold, E.4
-
26
-
-
0032980063
-
Preimplantation genetic diagnosis and sperm analysis by fluorescence in-situ hybridization for the most common reciprocal translocation t(11;22)
-
Van Assche E, Staesson C, Vegetti W et al: Preimplantation genetic diagnosis and sperm analysis by fluorescence in-situ hybridization for the most common reciprocal translocation t(11;22). Mol Hum Reprod 1999; 5: 682-690.
-
(1999)
Mol. Hum. Reprod.
, vol.5
, pp. 682-690
-
-
Van Assche, E.1
Staesson, C.2
Vegetti, W.3
-
27
-
-
0031879163
-
Preimplantation genetic analysis of translocations: Case-specific probes for interphase cell analysis
-
Munne S, Fung J, Cassel MJ, Marquez C, Weier HUG: 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.G.5
-
28
-
-
0032908816
-
Preimplantation genetic diagnosis for couples at high risk of Down syndrome pregnancy due to parental translocation or mosaicism
-
Conn CM, Cozzi J, Harper JC, Winston RML, Delhanty JDA: Preimplantation genetic diagnosis for couples at high risk of Down syndrome pregnancy due to parental translocation or mosaicism. J Med Genet 1999; 36: 45-50.
-
(1999)
J. Med. Genet.
, vol.36
, pp. 45-50
-
-
Conn, C.M.1
Cozzi, J.2
Harper, J.C.3
Winston, R.M.L.4
Delhanty, J.D.A.5
|