-
1
-
-
0031149814
-
The primordial germ cells of mammals: Some current perspectives
-
DOI 10.1006/excr.1997.3508
-
Buehr M: The primordial germ cells of mammals: some current perspectives. Exp Cell Res 232: 194-207 (1997). (Pubitemid 27194031)
-
(1997)
Experimental Cell Research
, vol.232
, Issue.2
, pp. 194-207
-
-
Buehr, M.1
-
2
-
-
0032971825
-
A trisomic germ cell line and precocious chromatid segregation leads to recurrent trisomy 21 conception
-
DOI 10.1007/s004390050905
-
Cozzi J, Conn CM, Harper J, Winston RML, Rindl M, et al: A trisomic germ cell line and precocious chromatid separation leads to recurrent trisomy 21 conception. Hum Genet 104: 23-28 (1999). (Pubitemid 29134637)
-
(1999)
Human Genetics
, vol.104
, Issue.1
, pp. 23-28
-
-
Cozzi, J.1
Conn, C.M.2
Harper, J.3
Winston, R.M.L.4
Rindl, M.5
Farndon, P.A.6
Delhanty, J.D.A.7
-
3
-
-
0035185798
-
Pseudo dicentric chromosome (5;21): A rare example of maternal germline mosaicism
-
Engel U, Bohlander SK, Bink K, Hinney B, Laccone F, Bartels I: Pseudo dicentric chromosome (5; 21): a rare example of maternal germline mosaicism. Hum Reprod 16: 63-66 (2001). (Pubitemid 32058581)
-
(2001)
Human Reproduction
, vol.16
, Issue.1
, pp. 63-66
-
-
Engel, U.1
Bohlander, S.K.2
Bink, K.3
Hinney, B.4
Laccone, F.5
Bartels, I.6
-
4
-
-
0033070152
-
Mosaicism and sporadic familial adenomatous polyposis
-
Farrington SM, Dunlop MG: Mosaicism and sporadic familial adenomatous polyposis. Am J Hum Genet 64: 653-658 (1999).
-
(1999)
Am J Hum Genet
, vol.64
, pp. 653-658
-
-
Farrington, S.M.1
Dunlop, M.G.2
-
5
-
-
33749547643
-
Comparative genomic hybridization analysis of human oocytes and polar bodies
-
DOI 10.1093/humrep/del157
-
Fragouli E, Wells D, Thornhill A, Serhal P, Faed MJW, et al: Comparative genomic hybridization analysis of human oocytes and polar bodies. Hum Reprod 21: 2319-2328 (2006). (Pubitemid 44530606)
-
(2006)
Human Reproduction
, vol.21
, Issue.9
, pp. 2319-2328
-
-
Fragouli, E.1
Wells, D.2
Thornhill, A.3
Serhal, P.4
Faed, M.J.W.5
Harper, J.C.6
Delhanty, J.D.A.7
-
6
-
-
12144267323
-
Mad2 prevents aneuploidy and premature proteolysis of cyclin B and securin during meiosis I in mouse oocytes
-
DOI 10.1101/gad.328105
-
Homer HA, McDougall A, Levasseur M, Yallop K, Murdoch AP, Herbert M: Mad2 prevents aneuploidy and premature proteolysis of cyclin B and securing during meiosis I in mouse oocytes. Genes Dev 19: 202-207 (2005). (Pubitemid 40111115)
-
(2005)
Genes and Development
, vol.19
, Issue.2
, pp. 202-207
-
-
Homer, H.A.1
McDougall, A.2
Levasseur, M.3
Yallop, K.4
Murdoch, A.P.5
Herbert, M.6
-
7
-
-
68049085066
-
On the origin of trisomy 21 Down syndrome
-
Hultén MA, Patel SD, Tankimanova M, Westgren M, Papadogiannakis N, et al: On the origin of trisomy 21 Down syndrome. Mol Cytogenet 1: 21 (2008).
-
(2008)
Mol Cytogenet
, vol.1
, pp. 21
-
-
Hultén, M.A.1
Patel, S.D.2
Tankimanova, M.3
Westgren, M.4
Papadogiannakis, N.5
-
8
-
-
77649331363
-
On the paternal origin of trisomy 21 Down Syndrome
-
Hultén MA, Patel SD, Westgren M, Papadogiannakis N, Jonsson AM, et al: On the paternal origin of trisomy 21 Down Syndrome. Mol Cytogenet 3: 4 (2010).
-
(2010)
Mol Cytogenet
, vol.3
, pp. 4
-
-
Hultén, M.A.1
Patel, S.D.2
Westgren, M.3
Papadogiannakis, N.4
Jonsson, A.M.5
-
9
-
-
0025270427
-
Confined placental mosaicism and intrauterine development
-
Kalousek DK: Confined placental mosaicism and intrauterine development. Pediatr Pathol 10: 69-77 (1990). (Pubitemid 20130954)
-
(1990)
Pediatric Pathology
, vol.10
, Issue.1-2
, pp. 69-77
-
-
Kalousek, D.K.1
-
10
-
-
34547533178
-
Bi-orientation of achiasmatic chromosomes in meiosis I oocytes contributes to aneuploidy in mice
-
DOI 10.1038/ng2065, PII NG2065
-
Kouznetsova A, Lister L, Nordenskjöld M, Herbert M, Höög C: Bi-orientation of achiasmatic chromosomes in meiosis I oocytes contributes to aneuploidy in mice. Nat Genet 39: 966-968 (2007). (Pubitemid 47185172)
-
(2007)
Nature Genetics
, vol.39
, Issue.8
, pp. 966-968
-
-
Kouznetsova, A.1
Lister, L.2
Nordenskjold, M.3
Herbert, M.4
Hoog, C.5
-
11
-
-
77951518762
-
Germ-line transmission of trisomy 21: Data from 80 families suggests an implication of grandmaternal age and a high frequency of female-specific trisomy rescue
-
Kovaleva NV: Germ-line transmission of trisomy 21: Data from 80 families suggests an implication of grandmaternal age and a high frequency of female-specific trisomy rescue. Mol Cytogenet 3: 7 (2010).
-
(2010)
Mol Cytogenet
, vol.3
, pp. 7
-
-
Kovaleva, N.V.1
-
13
-
-
0031425426
-
Lack of checkpoint control at the metaphase/anaphase transition: A mechanism of meiotic nondisjunction in mammalian females
-
DOI 10.1083/jcb.139.7.1611
-
LeMaire-Adkins R, Radke K, Hunt PA: Lack of checkpoint control at the metaphase/anaphase transition: a mechanism of meiotic nondisjunction in mammalian females. J Cell Biol 139: 1611-1619 (1997). (Pubitemid 28079227)
-
(1997)
Journal of Cell Biology
, vol.139
, Issue.7
, pp. 1611-1619
-
-
LeMaire-Adkins, R.1
Radke, K.2
Hunt, P.A.3
-
14
-
-
0018229617
-
Étude de la méiose ovocytaire chez un foetus trisomique 18
-
Luciani JM, Devictor M, Boué J, Morazzani MR, Boué A, Stahl A: Étude de la méiose ovocytaire chez un foetus trisomique 18. Ann Genet 21: 215-218 (1978).
-
(1978)
Ann Genet
, vol.21
, pp. 215-218
-
-
Luciani, J.M.1
Devictor, M.2
Boué, J.3
Morazzani, M.R.4
Boué, A.5
Stahl, A.6
-
15
-
-
0033943554
-
Mechanisms of maternal aneuploidy: FISH analysis of oocytes and polar bodies in patients undergoing assisted conception
-
DOI 10.1007/s004390050034
-
Mahmood R, Brierley CH, Faed MJ, Mills JA, Delhanty JD: Mechanisms of maternal aneuploidy: FISH analysis of oocytes and polar bodies in patients undergoing assisted conception. Hum Genet 106: 620-626 (2000). (Pubitemid 30427016)
-
(2000)
Human Genetics
, vol.106
, Issue.6
, pp. 620-626
-
-
Mahmood, R.1
Brierley, C.H.2
Faed, M.J.W.3
Mills, J.A.4
Delhanty, J.D.A.5
-
16
-
-
29244462029
-
Not all germ cells are created equal: Aspects of sexual dimorphism in mammalian meiosis
-
DOI 10.1530/rep.1.00865
-
Morelli M, Cohen P: Not all germ cells are created equal: aspects of sexual dimorphism in mammalian meiosis. Reproduction 130: 761-781 (2005). (Pubitemid 41830087)
-
(2005)
Reproduction
, vol.130
, Issue.6
, pp. 761-781
-
-
Morelli, M.A.1
Cohen, P.E.2
-
18
-
-
0037688075
-
Analysis of nine chromosome probes in first polar bodies and metaphase II oocytes for the detection of aneuploidies
-
DOI 10.1038/sj.ejhg.5200965
-
Pujol A, Boiso I, Benet J, Veiga A, Durban M, et al: Analysis of nine chromosome probes in first polar bodies and metaphase II oocytes for the detection of aneuploidies. Eur J Hum Genet 11: 325-336 (2003). (Pubitemid 36553491)
-
(2003)
European Journal of Human Genetics
, vol.11
, Issue.4
, pp. 325-336
-
-
Pujol, A.1
Boiso, I.2
Benet, J.3
Veiga, A.4
Durban, M.5
Campillo, M.6
Egozcue, J.7
Navarro, J.8
-
20
-
-
18744382409
-
Origin of amnion and implications for evaluation of the fetal genotype in cases of mosaicism
-
DOI 10.1002/pd.483
-
Robinson WP, McFadden DE, Barrett IJ, Kuchinka B, Peñaherrera MS, et al: Origin of amnion and implications for evaluation of the fetal genotype in cases of mosaicism. Prenat Diagn 22: 1076-1085 (2002). (Pubitemid 35448393)
-
(2002)
Prenatal Diagnosis
, vol.22
, Issue.12
, pp. 1076-1085
-
-
Robinson, W.P.1
McFadden, D.E.2
Barrett, I.J.3
Kuchinkal, B.4
Penaherrera, M.S.5
Bruyere, H.6
Best, R.G.7
Pedreira, D.A.L.8
Langlois, S.9
Kalousek, D.K.10
-
21
-
-
0026547503
-
Low level mosaicism for a balanced 7; 14 translocation in the father of an abnormal 7q+ child
-
Sciorra LJ, Schlenker E, Toke D, Brady-Yasbin S, Day-Salvatore D, Lee ML: Low level mosaicism for a balanced 7; 14 translocation in the father of an abnormal 7q+ child. Am J Med Genet 42: 296-297 (1992).
-
(1992)
Am J Med Genet
, vol.42
, pp. 296-297
-
-
Sciorra, L.J.1
Schlenker, E.2
Toke, D.3
Brady-Yasbin, S.4
Day-Salvatore, D.5
Lee, M.L.6
-
22
-
-
4344692091
-
Paternal gonadal mosaicism detected in a couple with recurrent abortions undergoing PGD: FISH analysis of sperm nuclei proves valuable
-
Somprasit C, Aguinaga M, Cisneros PL, Torsky S, Carson SA, et al: Paternal gonadal mosaicism detected in a couple with recurrent abortions undergoing PGD: FISH analysis of sperm nuclei proves valuable. Reprod BioMed Online 9: 225-230 (2004). (Pubitemid 39157489)
-
(2004)
Reproductive BioMedicine Online
, vol.9
, Issue.2
, pp. 225-230
-
-
Somprasit, C.1
Aguinaga, M.2
Cisneros, P.L.3
Torsky, S.4
Carson, S.A.5
Buster, J.E.6
Amato, P.7
McAdoo, S.L.8
Simpson, J.L.9
Bischoff, F.Z.10
-
23
-
-
0021359194
-
Meiotic configurations in female trisomy 21 foetuses
-
Speed RM: Meiotic configurations in female trisomy 21 foetuses. Hum Genet 66: 176-180 (1984). (Pubitemid 14142458)
-
(1984)
Human Genetics
, vol.66
, Issue.2-3
, pp. 176-180
-
-
Speed, R.M.1
-
24
-
-
0032472038
-
Molecular cytogenetic detection of confined gonadal mosaicism in a conceptus with trisomy 16 placental mosaicism [4]
-
DOI 10.1086/302149
-
Stavropoulos DJ, Bick D, Kalousek DK: Molecular cytogenetic detection of confined gonadal mosaicism in a conceptus with trisomy 16 placental mosaicism. Am J Hum Genet 63: 1912-1914 (1998). (Pubitemid 30415754)
-
(1998)
American Journal of Human Genetics
, vol.63
, Issue.6
, pp. 1912-1914
-
-
Stavropoulos, D.J.1
Bick, D.2
Kalousek, D.K.3
-
25
-
-
34547229205
-
An explanation for another familial case of Rett syndrome: Maternal germline mosaicism
-
DOI 10.1038/sj.ejhg.5201835, PII 5201835
-
Venâncio M, Santos M, Aires Pereira S, Maciel P, Saraiva JM: An explanation for another familial case of Rett syndrome: maternal germline mosaicism. Eur J Hum Genet 15: 902-904 (2007). (Pubitemid 47109052)
-
(2007)
European Journal of Human Genetics
, vol.15
, Issue.8
, pp. 902-904
-
-
Venancio, M.1
Santos, M.2
Pereira, S.A.3
Maciel, P.4
Saraiva, J.M.5
-
26
-
-
0034064674
-
Chromosome analysis of blastomeres from human embryos by using comparative genomic hybridization
-
DOI 10.1007/s004390051030
-
Voullaire L, Slater H, Williamson R, Wilton L: Chromosome analysis of blastomeres from human embryos using comparative genomic hybridization. Hum Genet 106: 210-217 (2000). (Pubitemid 30156426)
-
(2000)
Human Genetics
, vol.106
, Issue.2
, pp. 210-217
-
-
Voullaire, L.1
Slater, H.2
Williamson, R.3
Wilton, L.4
-
27
-
-
0033679573
-
Comprehensive chromosomal analysis of human preimplantation embryos using whole genome amplification and single cell comparative genomic hybridization
-
Wells D, Delhanty JD: Comprehensive chromosomal analysis of human preimplantation embryos using whole genome amplification and single cell comparative genomic hybridization. Mol Hum Reprod 6: 1055-1062 (2000).
-
(2000)
Mol Hum Reprod
, vol.6
, pp. 1055-1062
-
-
Wells, D.1
Delhanty, J.D.2
-
28
-
-
4644329601
-
Germline mosaicism complicates molecular diagnosis of Lesch-Nyban syndrome
-
DOI 10.1002/pd.959
-
Willers I: Germline mosaicism complicates molecular diagnosis of Lesch-Nyhan syndrome. Prenat Diagn 24: 737-740 (2004). (Pubitemid 39281137)
-
(2004)
Prenatal Diagnosis
, vol.24
, Issue.9
, pp. 737-740
-
-
Willers, I.1
|