-
1
-
-
0028926083
-
Clinical and molecular studies in full trisomy 22: Further delineation of the phenotype and review of the literature
-
Bacino CA, Schreck R, Fischel-Ghosdian N, Pepkowitz S, Prezant TR, Graham JM: Clinical and molecular studies in full trisomy 22: Further delineation of the phenotype and review of the literature. Am J Med Genet 56: 359-365 (1995).
-
(1995)
Am J Med Genet
, vol.56
, pp. 359-365
-
-
Bacino, C.A.1
Schreck, R.2
Fischel-Ghosdian, N.3
Pepkowitz, S.4
Prezant, T.R.5
Graham, J.M.6
-
3
-
-
27144547761
-
Array comparative genomic hybridization profiling of first-trimester spontaneous abortions that fail to grow in vitro
-
DOI 10.1002/pd.1230
-
Benkhalifa M, Kasakyan S, Clement P, Baldi M, Tachdjian G, et al: Array comparative genomic hybridization profiling of first-trimester spontaneous abortions that fail to grow in vitro. Prenat Diagn 25: 894-900 (2005). (Pubitemid 41494984)
-
(2005)
Prenatal Diagnosis
, vol.25
, Issue.10
, pp. 894-900
-
-
Benkhalifa, M.1
Kasakyan, S.2
Clement, P.3
Baldi, M.4
Tachdjian, G.5
Demirol, A.6
Gurgan, T.7
Florentino, F.8
Mohammed, M.9
Qumsiyeh, M.B.10
-
4
-
-
0028846477
-
Mosaicism for trisomy 12: Four cases with varying outcomes
-
Bischoff FZ, Zenger-Hain J, Moses D, Van Dyke DL, Shaffer LG: Mosaicism for trisomy 12: four cases with varying outcomes. Prenat Diagn 15: 1017-1026 (1995).
-
(1995)
Prenat Diagn
, vol.15
, pp. 1017-1026
-
-
Bischoff, F.Z.1
Zenger-Hain, J.2
Moses, D.3
Van Dyke, D.L.4
Shaffer, L.G.5
-
5
-
-
0031829015
-
Chromosomal anomalies in abnormal human pregnancies
-
DOI 10.1159/000020836
-
Brajenovic-Milic B, Petrovic O, Krasevic M, Ristic S, Kapovic M: Chromosomal anomalies in abnormal human pregnancies. Fetal Diagn Therapy 13: 187-191 (1998). (Pubitemid 28321286)
-
(1998)
Fetal Diagnosis and Therapy
, vol.13
, Issue.3
, pp. 187-191
-
-
Brajenovic-Milic, B.1
Petrovic, O.2
Krasevic, M.3
Ristic, S.4
Kapovic, M.5
-
6
-
-
6844265590
-
Non-disjunction of chromosome 18
-
Bugge M, Collins A, Petersen MB, Fisher J, Brandt C, et al: Non-disjunction of chromosome 18. Hum Mol Genet 7: 661-668 (1998).
-
(1998)
Hum Mol Genet
, vol.7
, pp. 661-668
-
-
Bugge, M.1
Collins, A.2
Petersen, M.B.3
Fisher, J.4
Brandt, C.5
-
7
-
-
15844378207
-
Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism
-
DOI 10.1002/(SICI)1097-0223(199604)16:4<323::AID-PD856>3.0.CO;2-5
-
Christian SL, Smith AC, Macha M, Black C, Elder FF, et al: Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism. Prenat Diagn 16: 323-332 (1996). (Pubitemid 26154544)
-
(1996)
Prenatal Diagnosis
, vol.16
, Issue.4
, pp. 323-332
-
-
Christian, S.L.1
Smith, A.C.M.2
Macha, M.3
Black, S.H.4
Elder, F.F.B.5
Johnson, J.M.-P.6
Resta, R.G.7
Surti, U.8
Suslak, L.9
Verp, M.S.10
Ledbetter, D.H.11
-
8
-
-
0023840501
-
An embryogenic model to explain cytogenetic inconsistencies observed in chorionic villus versus fetal tissue
-
Crane JP, Cheung SW: An embryonic model to explain cytogenetic inconsistencies observed in chorionic villus versus fetal tissue. Prenat Diagn 8: 119-129 (1988). (Pubitemid 18068786)
-
(1988)
Prenatal Diagnosis
, vol.8
, Issue.2
, pp. 119-129
-
-
Crane, J.P.1
Cheung, S.W.2
-
9
-
-
0031839349
-
Detection of chromosomal aberration in fetuses arising from recurrent spontaneous abortion by comparative genomic hybridization
-
DOI 10.1093/humrep/13.4.805
-
Daniely M, Aviram-Goldring A, Barkai G, Goldman B: Detection of chromosomal aberration in fetuses arising from recurrent spontaneous abortion by comparative genomic hybridization. Hum Reprod 13: 805-809 (1998). (Pubitemid 28239178)
-
(1998)
Human Reproduction
, vol.13
, Issue.4
, pp. 805-809
-
-
Daniely, M.1
Aviram-Goldring, A.2
Barkai, G.3
Goldman, B.4
-
10
-
-
0029052605
-
Double autosomal/gonosomal mosaic aneuploidy: Study of non-disjunction in two cases with trisomy of chromosome 8
-
De Brasi D, Genuardi M, D'Agostino A, Calvieri F, Tozzi C, et al: Double autosomal/gonosomal mosaic aneuploidy: Study of non-disjunction in two cases with trisomy of chromosome 8. Hum Genet 95: 519-525 (1995).
-
(1995)
Hum Genet
, vol.95
, pp. 519-525
-
-
De Brasi, D.1
Genuardi, M.2
D'Agostino, A.3
Calvieri, F.4
Tozzi, C.5
-
11
-
-
26244455545
-
Mechanisms of aneuploidy induction in human oogenesis and early embryogenesis
-
DOI 10.1159/000086894
-
Delhanty JDA: Mechanisms of aneuploidy induction in human oogenesis and early embryogenesis. Cytogenet Genome Res 111: 237-244 (2005). (Pubitemid 41414473)
-
(2005)
Cytogenetic and Genome Research
, vol.111
, Issue.3-4
, pp. 237-244
-
-
Delhanty, J.D.A.1
-
12
-
-
0026338577
-
Cytogenetic anomalies and placental function
-
Delozier-Blanchet CD: Cytogenetic anomalies and placental function. Rev Fr Gynecol Obstet 86: 723-729 (1991).
-
(1991)
Rev Fr Gynecol Obstet
, vol.86
, pp. 723-729
-
-
Delozier-Blanchet, C.D.1
-
13
-
-
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, et al: 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 47: 656-663 (1990).
-
(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
-
14
-
-
0028907505
-
Trisomy 18: Studies of the parent and cell division of origin and the effect of aberrant recombination on nondisjunction
-
Fisher JM, Harvey JF, Morton NE, Jacobs PA: Trisomy 18: studies of the parent and cell division of origin and the effect of aberrant recombination on nondisjunction. Am J Hum Genet 56: 669-675 (1995).
-
(1995)
Am J Hum Genet
, vol.56
, pp. 669-675
-
-
Fisher, J.M.1
Harvey, J.F.2
Morton, N.E.3
Jacobs, P.A.4
-
15
-
-
0014446261
-
Mosaicism and chimaeras
-
Ford CE: Mosaicism and chimaeras. Br Med Bull 25: 104-109 (1969).
-
(1969)
Br Med Bull
, vol.25
, pp. 104-109
-
-
Ford, C.E.1
-
16
-
-
0032977587
-
Mosaic trisomy 17 in amniocytes: Phenotypic outcome, tissue distribution, and uniparental disomy studies
-
DOI 10.1038/sj.ejhg.5200333
-
Genuardi M, Tozzi C, Pomponi M, Stagni M, Matteo DM, et al: Mosaic trisomy 17 in amniocytes: phenotypic outcome, tissue distribution, and uniparental disomy studies. Eur J Hum Genet 7: 421-426 (1997). (Pubitemid 29261327)
-
(1999)
European Journal of Human Genetics
, vol.7
, Issue.4
, pp. 421-426
-
-
Genuardi, M.1
Tozzi, C.2
Pomponi, M.G.3
Stagni, M.L.4
Della Monica, M.5
Scarano, G.6
Calvieri, F.7
Torrisi, L.8
Neri, G.9
-
17
-
-
0030770715
-
Cytogenetic analysis of spontaneous abortions: Comparison of techniques and assessment of the incidence of confined placental mosaicism
-
DOI 10.1002/(SICI)1096-8628(19971031)72:3<297::AID-AJMG9>3.0.CO;2-O
-
Griffin DK, Millie EA, Redline RW, Hassold TJ, Zaragoza MV: Cytogenetic analysis of spontaneous abortions: Comparison of techniques and assessment of the incidence of confined placental mosaicism. Am J Med Genet 72: 297-301 (1997). (Pubitemid 27424233)
-
(1997)
American Journal of Medical Genetics
, vol.72
, Issue.3
, pp. 297-301
-
-
Griffin, D.K.1
Millie, E.A.2
Redline, R.W.3
Hassold, T.J.4
Zaragoza, M.V.5
-
18
-
-
0023578832
-
Prevalence and distribution of chromosome abnormalities in a sample of first trimester internal abortions
-
Guerneri S, Bettio D, Simoni G, Brambati B, Lanzani A, Fraccaro M: Prevalence and distribution of chromosome abnormalities in a sample of first trimester internal abortions. Hum Reprod 2: 735-739 (1987). (Pubitemid 18012884)
-
(1987)
Human Reproduction
, vol.2
, Issue.8
, pp. 735-739
-
-
Guerneri, S.1
Bettio, D.2
Simoni, G.3
Brambati, B.4
Lanzani, A.5
Fraccaro, M.6
-
19
-
-
0030941126
-
European collaborative research on mosaicism in CVS (EUCROMIC) - Fetal and extrafetal cell lineages in 192 gestations with CVS mosaicism involving single autosomal trisomy
-
DOI 10.1002/(SICI)1096-8628(19970516)70:2<179::AID-AJMG15>3.0.CO;2- G
-
Hahnemann JM, Vejerslev LO: European collaborative research on mosaicism in CVS (EUROCROMIC) - fetal and extrafetal cell lineages in 192 gestations with CVS mosaicism involving single autosomal trisomy. Am J Med Genet 70: 179-187 (1997). (Pubitemid 27184576)
-
(1997)
American Journal of Medical Genetics
, vol.70
, Issue.2
, pp. 179-187
-
-
Hahnemann, J.M.1
Vejerslev, L.O.2
-
20
-
-
0035319804
-
To err (meiotically) is human: The genesis of human aneuploidy
-
DOI 10.1038/35066065
-
Hassold T, Hunt P: To err (meiotically) is human: the genesis of human aneuploidy. Nat Rev Genet 2: 280-291 (2001). (Pubitemid 33674776)
-
(2001)
Nature Reviews Genetics
, vol.2
, Issue.4
, pp. 280-291
-
-
Hassold, T.1
Hunt, P.2
-
21
-
-
0024398336
-
Analysis of non-disjunction in human trisomic spontaneous abortions
-
Hassold T, Takaesu N: Analysis of non-disjunction in human trisomic spontaneous abortions. Prog Clin Biol Res 311: 115-134 (1989).
-
(1989)
Prog Clin Biol Res
, vol.311
, pp. 115-134
-
-
Hassold, T.1
Takaesu, N.2
-
22
-
-
0019198839
-
A cytogenetic study of 1000 spontaneous abortions
-
Hassold T, Chen N, Funkhouser J, Jooss T, Manuel B, et al: A cytogenetic study of 1000 spontaneous abortions. Ann Hum Genet 44: 151-178 (1980). (Pubitemid 11215107)
-
(1980)
Annals of Human Genetics
, vol.44
, Issue.2
, pp. 151-178
-
-
Hassold, T.1
Chen, N.2
Funkhouser, J.3
-
23
-
-
0023516778
-
Cytogenetic and molecular studies of trisomy 13
-
Hassold T, Jacobs PA, Leppert M, Sheldon M: Cytogenetic and molecular studies of trisomy 13. J Med Genet 24: 725-732 (1987). (Pubitemid 18002274)
-
(1987)
Journal of Medical Genetics
, vol.24
, Issue.12
, pp. 725-732
-
-
Hassold, T.1
Jacobs, P.A.2
Leppert, M.3
Sheldon, M.4
-
24
-
-
0026030223
-
Molecular studies of non-disjunction in trisomy 16
-
Hassold T, Pettay D, Freeman SD, Grantham M, Takaesu N: Molecular studies of non-disjunction in trisomy 16. J Med Genet 28: 159-162 (1991). (Pubitemid 21922575)
-
(1991)
Journal of Medical Genetics
, vol.28
, Issue.3
, pp. 159-162
-
-
Hassold, T.J.1
Pettay, D.2
Freeman, S.B.3
Grantham, M.4
Takaesu, N.5
-
25
-
-
0029118422
-
Recombination and maternalage dependent nondisjunction: Molecular studies of trisomy 16
-
Hassold T, Merrill M, Adkins K, Freeman S, Sherman S: Recombination and maternalage dependent nondisjunction: molecular studies of trisomy 16. Am J Hum Genet 57: 867-874 (1995).
-
(1995)
Am J Hum Genet
, vol.57
, pp. 867-874
-
-
Hassold, T.1
Merrill, M.2
Adkins, K.3
Freeman, S.4
Sherman, S.5
-
26
-
-
0030049019
-
Molecular studies of the aetiology of trisomy 8 in spontaneous abortions and the liveborn population
-
DOI 10.1007/BF02185754
-
James RS, Jacobs PA: Molecular studies of the aetiology of trisomy 8 in spontaneous abortions and the liveborn population. Hum Genet 97: 283-286 (1996). (Pubitemid 26057022)
-
(1996)
Human Genetics
, vol.97
, Issue.3
, pp. 283-286
-
-
James, R.S.1
Jacobs, P.A.2
-
27
-
-
0018887287
-
Anatomic and chromosomal anomalies in 639 spontaneous abortuses
-
Kajii T, Ferrier A, Niikawa N, Takahara H, Ohama K, Avirachan S: Anatomic and chromosomal abnormalities in 639 spontaneous abortuses. Hum Genet 55: 87-98 (1980). (Pubitemid 10090195)
-
(1980)
Human Genetics
, vol.55
, Issue.1
, pp. 87-98
-
-
Kajii, T.1
Ferrier, A.2
Niikawa, N.3
-
28
-
-
0034049607
-
Pathogenesis of chromosomal mosaicism and its effect on early human development
-
DOI 10.1002/(SICI)1096-8628(20000306)91:1<39::AID-AJMG7>3.0.CO;2-L
-
Kalousek DK: Pathogenesis of chromosomal mosaicism and its effect on early human development. Am J Hum Genet 91: 39-45 (2000). (Pubitemid 30127557)
-
(2000)
American Journal of Medical Genetics
, vol.91
, Issue.1
, pp. 39-45
-
-
Kalousek, D.K.1
-
29
-
-
0020606517
-
Chromosomal mosaicism confined to the placenta in human conceptions
-
Kalousek DK, Dill FJ: Chromosomal mosaicism confined to the placenta in human conceptions. Science 221: 665-667 (1983). (Pubitemid 13026084)
-
(1983)
Science
, vol.221
, Issue.4611
, pp. 665-667
-
-
Kalousek, D.K.1
Dill, F.J.2
-
31
-
-
0026560379
-
Spontaneous abortions and confined placental mosaicism
-
Kalousek DK, Barrett IJ, Gartner AB: Spontaneous abortions and confined placental mosaicism. Hum Genet 88: 642-646 (1992).
-
(1992)
Hum Genet
, vol.88
, pp. 642-646
-
-
Kalousek, D.K.1
Barrett, I.J.2
Gartner, A.B.3
-
32
-
-
0029852041
-
Trisomy 7 CVS mosaicism: Pregnancy outcome, placental and DNA analysis in 14 cases
-
Kalousek DK, Langlois S, Robison WP, Telenius A, Bernard L, et al: Trisomy 7 CVS mosaicism: pregnancy outcome, placental and DNA analysis in 14 cases. Am J Med Genet 65: 348-352 (1996).
-
(1996)
Am J Med Genet
, vol.65
, pp. 348-352
-
-
Kalousek, D.K.1
Langlois, S.2
Robison, W.P.3
Telenius, A.4
Bernard, L.5
-
33
-
-
13144259703
-
Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism
-
Karadima G, Bugge M, Nicolaidis P, Vassilopoulos D, Avramopoulos D, et al: Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism. Eur J Hum Genet 6: 432-438 (1998). (Pubitemid 28486337)
-
(1998)
European Journal of Human Genetics
, vol.6
, Issue.5
, pp. 432-438
-
-
Karadima, G.1
Bugge, M.2
Nicolaidis, P.3
Vassilopoulos, D.4
Avramopoulos, D.5
Grigoriadou, M.6
Albrecht, B.7
Passarge, E.8
Anneren, G.9
Blennow, E.10
Clausen, N.11
Galla-Voumvouraki, A.12
Tsezou, A.13
Kitsiou-Tzeli, S.14
Hahnemann, J.M.15
Hertz, J.M.16
Houge, G.17
Kuklik, M.18
Macek, M.19
Lacombe, D.20
Miller, K.21
Moncla, A.22
Pajares, I.L.23
Patsalis, P.C.24
Prieur, M.25
Vekemans, M.26
Von Beust, G.27
Brondum-Nielsen, K.28
Petersen, M.B.29
more..
-
34
-
-
0345521056
-
Epidemiology of chromosomal anomalies in spontaneous abortion: Prevalence, manifestation and determinants
-
Bennett MJ, Edmonds DK (eds), Blackwell Scientific Publishers, Oxford
-
Kline J, Stein Z: Epidemiology of chromosomal anomalies in spontaneous abortion: Prevalence, manifestation and determinants, in Bennett MJ, Edmonds DK (eds): Spontaneous and Recurrent Abortion, pp 29-50 (Blackwell Scientific Publishers, Oxford 1987).
-
(1987)
Spontaneous and Recurrent Abortion
, pp. 29-50
-
-
Kline, J.1
Stein, Z.2
-
35
-
-
10544226872
-
Susceptible chiasmate configurations of chromosome 21 predispose to non- disjunction in both maternal meiosis I and meiosis II
-
DOI 10.1038/ng1296-400
-
Lamb NE, Freeman SB, Savage-Austin A, Pettay D, Taft L, Hersey J: Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II. Nat Genet 14: 400-405 (1996). (Pubitemid 26414583)
-
(1996)
Nature Genetics
, vol.14
, Issue.4
, pp. 400-405
-
-
Lamb, N.E.1
Freeman, S.B.2
Savage-Austin, A.3
Pettay, D.4
Taft, L.5
Hersey, J.6
Gu, Y.7
Shen, J.8
Saker, D.9
May, K.M.10
Avramopoulos, D.11
Petersen, M.B.12
Hallberg, A.13
Mikkelsen, M.14
Hassold, T.J.15
Sherman, S.L.16
-
36
-
-
4043128880
-
Features of chromosomal abnormalities in spontaneous abortion cell culture failures detected by interphase FISH analysis
-
DOI 10.1038/sj.ejhg.5201178
-
Lebedev IN, Ostroverkhova NV, Nikitina TV, Sukhanova NN, Nazarenko SA: Features of chromosomal abnormalities in spontaneous abortion cell culture failures detected by interphase FISH analysis. Eur J Hum Genet 12: 513-520 (2004). (Pubitemid 39077158)
-
(2004)
European Journal of Human Genetics
, vol.12
, Issue.7
, pp. 513-520
-
-
Lebedev, I.N.1
Ostroverkhova, N.V.2
Nikitina, T.V.3
Sukhanova, N.N.4
Nazarenko, S.A.5
-
37
-
-
0026682553
-
Cytogenetic results from the U.S. collaborative study on CVS
-
Ledbetter DH, Zachary JM, Simpson JL, Golbus MS, Pergament E, et al: Cytogenetic results from the U.S. collaborative study on CVS. Prenat Diagn 12: 317-345 (1992).
-
(1992)
Prenat Diagn
, vol.12
, pp. 317-345
-
-
Ledbetter, D.H.1
Zachary, J.M.2
Simpson, J.L.3
Golbus, M.S.4
Pergament, E.5
-
39
-
-
18344393473
-
Incidence and spectrum of chromosome abnormalities in spontaneous abortions: New insights from a 12-year study
-
DOI 10.1097/01.GIM.0000160075.96707.04
-
Menasha J, Levy B, Hirschhorn K, Kardon NB: Incidence and spectrum of chromosomal abnormalities in spontaneous abortions: New insights from a 12-year study. Genet Med 7: 251-263 (2005). (Pubitemid 40638071)
-
(2005)
Genetics in Medicine
, vol.7
, Issue.4
, pp. 251-263
-
-
Menasha, J.1
Levy, B.2
Hirschhorn, K.3
Kardon, N.B.4
-
40
-
-
0020447841
-
Parental origin of chromosome abnormalities in spontaneous abortions
-
Meulenbroeck GHM, Geraedts JPM: Parental origin of chromosome abnormalities in spontaneous abortions. Hum Genet 62: 129-133 (1982). (Pubitemid 13221420)
-
(1982)
Human Genetics
, vol.62
, Issue.2
, pp. 129-133
-
-
Meulenbroek, G.H.M.1
Geraedts, J.P.M.2
-
41
-
-
0027234613
-
Cytogenetic findings in echographically defined blighted ovum abortions
-
Minelli E, Buchi C, Granata P, Meroni E, Righi R, et al: Cytogenetic findings in echographically defined blighted ovum abortions. Ann Genet 36: 107-110 (1993). (Pubitemid 23276144)
-
(1993)
Annales de Genetique
, vol.36
, Issue.2
, pp. 107-110
-
-
Minelli, E.1
Buchi, C.2
Granata, P.3
Meroni, E.4
Righi, R.5
Portentoso, P.6
Giudici, A.7
Ercoli, A.8
Sartor, M.G.9
Rossi, A.10
Fasola, M.11
Campagna, C.12
Casalone, R.13
-
42
-
-
0031890840
-
Origin and mechanisms of non-disjunction in human autosomal trisomies
-
Nicolaidis P, Petersen MB: Origin and mechanisms of non-disjunction in human autosomal trisomies. Hum Reprod 13: 313-319 (1998).
-
(1998)
Hum Reprod
, vol.13
, pp. 313-319
-
-
Nicolaidis, P.1
Petersen, M.B.2
-
43
-
-
0026057960
-
A cytogenetic study of spontaneous abortions with direct analysis of chorionic villi
-
Ohno M, Maeda T, Matsunobi A: A cytogenetic study of spontaneous abortions with direct analysis of chorionic villi. Obstet Gynecol 77: 394-398 (1991).
-
(1991)
Obstet Gynecol
, vol.77
, pp. 394-398
-
-
Ohno, M.1
Maeda, T.2
Matsunobi, A.3
-
44
-
-
0028036242
-
Understanding the mechanism(s) of mosaic trisomy 21 by using DNA polymorphism analysis
-
Pangalos C, Avramopoulos D, Blouin JL, Raoul O, de Blois MC, et al: Understanding mechanism(s) of mosaic trisomy 21 by using DNA polymorphism analysis. Am J Hum Genet 54: 473-481 (1994). (Pubitemid 24068228)
-
(1994)
American Journal of Human Genetics
, vol.54
, Issue.3
, pp. 473-481
-
-
Pangalos, C.1
Avramopoulos, D.2
Blouin, J.-L.3
Raoul, O.4
DeBlois, M.-C.5
Prieur, M.6
Schinzel, A.A.7
Gika, M.8
Abazis, D.9
Antonarakis, S.E.10
-
45
-
-
0024322076
-
Is there a correlation between morphological and cytogenetic findings in placental tissue from early missed abortions?
-
Rehder H, Coerdt W, Eggert R, Klink F, Schwinger E: Is there a correlation between morphological and cytogenetic findings in placental tissue from early missed abortions? Hum Genet 82: 377-385 (1989). (Pubitemid 19181977)
-
(1989)
Human Genetics
, vol.82
, Issue.4
, pp. 377-385
-
-
Rehder, H.1
Coerdt, W.2
Eggers, R.3
Klink, F.4
Schwinger, E.5
-
46
-
-
16944367292
-
Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction
-
Robinson WP, Barrett IJ, Bernard L, Telenius A, Bernasconi F, et al: Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast and increased risk of fetal intrauterine growth restriction. Am J Hum Genet 60: 917-927 (1997). (Pubitemid 27146501)
-
(1997)
American Journal of Human Genetics
, vol.60
, Issue.4
, pp. 917-927
-
-
Robinson, W.P.1
Barrett, I.J.2
Bernard, L.3
Telenius, A.4
Bernasconi, F.5
Wilson, R.D.6
Best, R.G.7
Howard-Peebles, P.N.8
Langlois, S.9
Kalousek, D.K.10
-
47
-
-
0033532078
-
Frequency of meiotic trisomy depends on involved chromosome and mode of ascertainment
-
DOI 10.1002/(SICI)1096-8628(19990507)84:1<34::AID-AJMG8>3.0.CO;2-7
-
Robinson WP, Bernasconi F, Lau A, McFadden DE: Frequency of meiotic trisomy depends on involved chromosome and mode of ascertainment. Am J Med Genet 88: 34-42 (1999). (Pubitemid 29169232)
-
(1999)
American Journal of Medical Genetics
, vol.84
, Issue.1
, pp. 34-42
-
-
Robinson, W.P.1
Bernasconi, F.2
Lau, A.3
McFadden, D.E.4
-
48
-
-
0026000975
-
Trisomy 21: Association between reduced recombination and nondisjunction
-
Sherman SL, Takaesu N, Freeman SB, Grantham M, Phillips C, et al: Trisomy 21: association between reduced recombination and nondisjunction. Am J Hum Genet 49: 608-620 (1991). (Pubitemid 21891706)
-
(1991)
American Journal of Human Genetics
, vol.49
, Issue.3
, pp. 608-620
-
-
Sherman, S.L.1
Takaesu, N.2
Freeman, S.B.3
Grantham, M.4
Phillips, C.5
Blackston, R.D.6
Jacobs, P.A.7
Cockwell, A.E.8
Freeman, V.9
Uchida, I.10
Mikkelsen, M.11
Kurnit, D.M.12
Buraczynska, M.13
Keats, B.J.B.14
Hassold, T.J.15
-
49
-
-
0028675022
-
Confined placental mosaicism
-
Simoni G, Sirchia SM: Confined placental mosaicism. Prenat Diagn 14: 1185-1189 (1994).
-
(1994)
Prenat Diagn
, vol.14
, pp. 1185-1189
-
-
Simoni, G.1
Sirchia, S.M.2
-
51
-
-
33746129843
-
Probable origins, pregnancy outcome and risk of fetal UPD: European Collaborative Research on Mosaicism in CVS (EUCROMIC)
-
Trisomy CPM: probable origins, pregnancy outcome and risk of fetal UPD: European Collaborative Research on Mosaicism in CVS (EUCROMIC). Prenat Diagn 19: 29-35 (1999).
-
(1999)
Prenat Diagn
, vol.19
, pp. 29-35
-
-
Trisomy, C.P.M.1
-
52
-
-
14844304699
-
Evidence for high frequency of chromosomal mosaicism in spontaneous abortions revealed by interphase FISH analysis
-
DOI 10.1369/jhc.4A6424.2005
-
Vorsanova SG, Kolotii AD, Iourov IY, Monakhov VV, Kirillova EA, et al: Evidence for high frequency of chromosomal mosaicism in spontaneous abortions revealed by interphase FISH analysis. J Histochem Cytochem 53: 375-380 (2005). (Pubitemid 40344079)
-
(2005)
Journal of Histochemistry and Cytochemistry
, vol.53
, Issue.3
, pp. 375-380
-
-
Vorsanova, S.G.1
Kolotii, A.D.2
Iourov, I.Y.3
Monakhov, V.V.4
Kirillova, E.A.5
Soloviev, I.V.6
Yurov, Y.B.7
-
53
-
-
84961014776
-
Spontaneous abortion risks in man: Data from reproductive histories in a medical genetics unit
-
Warburton D, Fraser FC: Spontaneous abortion risks in man: data from reproductive histories in a medical genetics unit. Am J Hum Genet 16: 1-24 (1964).
-
(1964)
Am J Hum Genet
, vol.16
, pp. 1-24
-
-
Warburton, D.1
Fraser, F.C.2
-
54
-
-
0018257650
-
Mosaic autosomal trisomy in cultures from spontaneous abortions
-
Warburton D, Yu CY, Kline J, Stein Z: Mosaic autosomal trisomy in cultures from spontaneous abortions. Am J Hum Genet 30: 609-617 (1978). (Pubitemid 9133201)
-
(1978)
American Journal of Human Genetics
, vol.30
, Issue.6
, pp. 609-617
-
-
Warburton, D.1
Yu, C.2
Kline, J.3
Stein, Z.4
-
55
-
-
0029886674
-
A case of maternal uniparental disomy of chromosome 9 in association with confined placental mosaicism for trisomy 9
-
DOI 10.1002/(SICI)1097-0223(199604)16:4<371::AID-PD866>3.0.CO;2-S
-
Wilkinson TA, James RS, Crolla JA, Cockwell AE, Cambell PL, Temple IK: A case of maternal uniparental disomy of chromosome 9 in association with confined placental mosaicism for trisomy 9. Prenat Diagn 16: 371-374 (1996). (Pubitemid 26154555)
-
(1996)
Prenatal Diagnosis
, vol.16
, Issue.4
, pp. 371-374
-
-
Wilkinson, T.A.1
James, R.S.2
Crolla, J.A.3
Cockwell, A.E.4
Campbell, P.L.5
Temple, I.K.6
-
56
-
-
0029950129
-
Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16, and 22: Their incidence, likely origins, and mechanisms for cell lineage compartmentalization
-
DOI 10.1002/(SICI)1097-0223(199606)16:6<511::AID-PD904>3.0.CO;2-8
-
Wolstenholme J: Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16 and 22: their incidence, likely origins and mechanisms for cell lineage compartmentalization. Prenat Diagn 16: 511-524 (1996). (Pubitemid 26187701)
-
(1996)
Prenatal Diagnosis
, vol.16
, Issue.6
, pp. 511-524
-
-
Wolstenholme, J.1
-
57
-
-
0028290914
-
Confined placental mosaicism, IUGR, and adverse pregnancy outcome: A controlled retrospective U.K. collaborative survey
-
DOI 10.1002/pd.1970140505
-
Wolstenholme J, Rooney DE, Davison EV: Confined placental mosaicism, IUGR and adverse pregnancy outcome: a controlled retrospective U.K. collaborative study. Prenat Diagn 14: 345-361 (1994). (Pubitemid 24178852)
-
(1994)
Prenatal Diagnosis
, vol.14
, Issue.5
, pp. 345-361
-
-
Wolstenholme, J.1
Rooney, D.E.2
Davison, E.V.3
-
58
-
-
0027937004
-
Nondisjunction of human acrocentric chromosomes: Studies of 432 trisomic fetuses and liveborns
-
Zaragoza MV, Jacobs PA, James RS, Rogan P, Sherman S, Hassold TJ: Nondisjunction of human acrocentric chromosomes: studies of 432 fetuses and liveborns. Hum Genet 94: 411-417 (1994). (Pubitemid 24297729)
-
(1994)
Human Genetics
, vol.94
, Issue.4
, pp. 411-417
-
-
Zaragoza, M.V.1
Jacobs, P.A.2
James, R.S.3
Rogan, P.4
Sherman, S.5
Hassold, T.6
-
59
-
-
0031791685
-
Studies of non-disjunction in trisomies 2, 7, 15, and 22: Does the parental origin of trisomy influence placental morphology?
-
Zaragoza MV, Millie E, Redline RW, Hassold TJ: Studies of non-disjunction in trisomies 2, 7, 15 and 22: does the parental origin of trisomy influence placental morphology? J Med Genet 35: 924-931 (1998). (Pubitemid 28486621)
-
(1998)
Journal of Medical Genetics
, vol.35
, Issue.11
, pp. 924-931
-
-
Zaragoza, M.V.1
Millie, E.2
Redline, R.W.3
Hassold, T.J.4
|