-
1
-
-
0028244914
-
Cytogenetic analysis of chorionic villi for prenatal diagnosis: An ACC collaborative study of U.K. data
-
Association of Clinical Cytogeneticists Working Party on Chorionic Villi in Prenatal Diagnosis (1994): Cytogenetic analysis of chorionic villi for prenatal diagnosis: An ACC collaborative study of U.K. data. Prenat Diagn 14:363-379.
-
(1994)
Prenat Diagn
, vol.14
, pp. 363-379
-
-
-
2
-
-
0026445152
-
Association between confined placental trisomy, fetal uniparental disomy, and early intrauterine growth retardation
-
Bennett P, Vaughan J, Henderson D, Loughna S, Moore G (1992): Association between confined placental trisomy, fetal uniparental disomy, and early intrauterine growth retardation. Lancet 340:1284-1285.
-
(1992)
Lancet
, vol.340
, pp. 1284-1285
-
-
Bennett, P.1
Vaughan, J.2
Henderson, D.3
Loughna, S.4
Moore, G.5
-
3
-
-
0026629938
-
Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy
-
Cassidy SB, Lai L, Erickson RP, Magnuson L, Thomas E, Gendron R, Herrmann J (1992): Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy. Am J Hum Genet 51:701-708.
-
(1992)
Am J Hum Genet
, vol.51
, pp. 701-708
-
-
Cassidy, S.B.1
Lai, L.2
Erickson, R.P.3
Magnuson, L.4
Thomas, E.5
Gendron, R.6
Herrmann, J.7
-
4
-
-
0028211039
-
Trisomy 12 mosaicism in a 7-year-old girl with dysmorphic features and normal mental development
-
English CJ, Goodship JA, Jackson A, Lowry M, Wolstenholme J (1994): Trisomy 12 mosaicism in a 7-year-old girl with dysmorphic features and normal mental development. J Med Genet 31:253-254.
-
(1994)
J Med Genet
, vol.31
, pp. 253-254
-
-
English, C.J.1
Goodship, J.A.2
Jackson, A.3
Lowry, M.4
Wolstenholme, J.5
-
5
-
-
0029077269
-
Maternal uniparental disomy of chromosome 2 in a baby with trisomy 2 mosaicism in amniotic fluid culture
-
Harrison K, Eisenger K, Anyane-Yeboa K, Brown S (1995): Maternal uniparental disomy of chromosome 2 in a baby with trisomy 2 mosaicism in amniotic fluid culture. Am J Med Genet 58:147-151.
-
(1995)
Am J Med Genet
, vol.58
, pp. 147-151
-
-
Harrison, K.1
Eisenger, K.2
Anyane-Yeboa, K.3
Brown, S.4
-
6
-
-
0025753402
-
A revisit of trisomy 20 mosaicism in prenatal diagnosis - An overview of 103 cases
-
Hsu LYF, Kaffe S, Perlis TE (1991): A revisit of trisomy 20 mosaicism in prenatal diagnosis - an overview of 103 cases. Prenat Diagn 11:7-15.
-
(1991)
Prenat Diagn
, vol.11
, pp. 7-15
-
-
Hsu, L.Y.F.1
Kaffe, S.2
Perlis, T.E.3
-
7
-
-
0002711242
-
Mosaicism confined to chorionic tissue in human gestations
-
Fraccaro M, ed. Berlin: Springer-Verlag
-
Kalousek DK (1985): Mosaicism confined to chorionic tissue in human gestations. In "First Trimester Fetal Diagnosis." Fraccaro M, ed. Berlin: Springer-Verlag, pp 130-136.
-
(1985)
First Trimester Fetal Diagnosis
, pp. 130-136
-
-
Kalousek, D.K.1
-
9
-
-
0027474269
-
Uniparental disomy for chromosome 16 in humans
-
Kalousek DK, Langlois S, Barrett I, Yam I, Wilson DR, Howard Peebles PN, Johnson MP, Giorgiutti E (1993): Uniparental disomy for chromosome 16 in humans. Am J Hum Genet 52:8-16.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 8-16
-
-
Kalousek, D.K.1
Langlois, S.2
Barrett, I.3
Yam, I.4
Wilson, D.R.5
Howard Peebles, P.N.6
Johnson, M.P.7
Giorgiutti, E.8
-
10
-
-
0028867372
-
Prenatal and postnatal growth failure associated with maternal heterodisomy for chromosome 7
-
Langlois S, Yong SL, Wilson RD, Kalousek DK (1995): Prenatal and postnatal growth failure associated with maternal heterodisomy for chromosome 7. J Med Genet 32:871-875.
-
(1995)
J Med Genet
, vol.32
, pp. 871-875
-
-
Langlois, S.1
Yong, S.L.2
Wilson, R.D.3
Kalousek, D.K.4
-
11
-
-
0026682553
-
Cytogenetic results from the U.S. Collaborative Study on CVS
-
Ledbetter DH, Zachary JM, Simpson JL, Golbus MS, Pergament E, Jackson L, Mahoney MJ, Desnick RJ, Schulman J, Copeland KL, et al. (1992): Cytogenetic results from the U.S. Collaborative Study on CVS. Prenat Diagn 12:317-345.
-
(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
Jackson, L.6
Mahoney, M.J.7
Desnick, R.J.8
Schulman, J.9
Copeland, K.L.10
-
12
-
-
0018198093
-
Manufactured hexaparental mice show that adults are derived from three embryonic cells
-
Markert CL, Petters RM (1978): Manufactured hexaparental mice show that adults are derived from three embryonic cells. Science 202:56-58.
-
(1978)
Science
, vol.202
, pp. 56-58
-
-
Markert, C.L.1
Petters, R.M.2
-
13
-
-
0025767956
-
Medical Research Council European Trial of chorion villus sampling
-
MRC Working Party On the Evaluation of Chorionic Villus Sampling (1991): Medical Research Council European Trial of chorion villus sampling. Lancet 337:1491-1499.
-
(1991)
Lancet
, vol.337
, pp. 1491-1499
-
-
-
14
-
-
0028207074
-
The predictive value of cytogenetic diagnosis after CVS based on 4860 cases with both direct and culture methods
-
Pittalis MC, Dalpra L, Torricelli F, Rizzo N, Nocera G, Cariati E, Santarini L, Tibiletti MG, Agosti S, Bovicelli L, Forabosco A (1994): The predictive value of cytogenetic diagnosis after CVS based on 4860 cases with both direct and culture methods. Prenat Diagn 14:267-278.
-
(1994)
Prenat Diagn
, vol.14
, pp. 267-278
-
-
Pittalis, M.C.1
Dalpra, L.2
Torricelli, F.3
Rizzo, N.4
Nocera, G.5
Cariati, E.6
Santarini, L.7
Tibiletti, M.G.8
Agosti, S.9
Bovicelli, L.10
Forabosco, A.11
-
15
-
-
0026680691
-
Uniparental disomy 15 resulting from "correction" of an initial trisomy 15
-
Purvis-Smith SG, Saville T, Manass S, Yip MY, Lam Po Tang PR, Duffy B, Johnston H, Leigh D, McDonald B (1992): Uniparental disomy 15 resulting from "correction" of an initial trisomy 15 [Letter]. Am J Hum Genet 50:1348-1350.
-
(1992)
Am J Hum Genet
, vol.50
, pp. 1348-1350
-
-
Purvis-Smith, S.G.1
Saville, T.2
Manass, S.3
Yip, M.Y.4
Lam Po Tang, P.R.5
Duffy, B.6
Johnston, H.7
Leigh, D.8
McDonald, B.9
-
16
-
-
0027981768
-
True trisomy 15 mosaicism, detected by amniocentesis at 12 weeks of gestation and fetal echocardiography
-
Sundberg K, Brocks V, Ramsøe Jacobsen J, Beck B (1994): True trisomy 15 mosaicism, detected by amniocentesis at 12 weeks of gestation and fetal echocardiography. Prenat Diagn 14:559-563.
-
(1994)
Prenat Diagn
, vol.14
, pp. 559-563
-
-
Sundberg, K.1
Brocks, V.2
Ramsøe Jacobsen, J.3
Beck, B.4
-
17
-
-
0026856030
-
Canadian multicenter randomized clinical trial of chorion villus sampling and amniocentesis. Chromosome mosaicism in CVS and amniocentesis samples
-
Teshima IE, Kalousek DK, Vekemans MJJ, Markovic V, Cox DM, Dallaire L, Gagne R, Lin JCC, Ray M, Sergovich FR, Uchida IA, Wang H, Tomkins DJ (1992): Canadian multicenter randomized clinical trial of chorion villus sampling and amniocentesis. Chromosome mosaicism in CVS and amniocentesis samples. Prenat Diagn 12:443-466.
-
(1992)
Prenat Diagn
, vol.12
, pp. 443-466
-
-
Teshima, I.E.1
Kalousek, D.K.2
Vekemans, M.J.J.3
Markovic, V.4
Cox, D.M.5
Dallaire, L.6
Gagne, R.7
Lin, J.C.C.8
Ray, M.9
Sergovich, F.R.10
Uchida, I.A.11
Wang, H.12
Tomkins, D.J.13
-
18
-
-
0027941823
-
Human uniparental disomy for chromosome 16 and fetal development
-
Vaughan J, Ali Z, Bower S, Bennett P, Chard T, Moore G (1994): Human uniparental disomy for chromosome 16 and fetal development. Prenat Diagn 14:751-756.
-
(1994)
Prenat Diagn
, vol.14
, pp. 751-756
-
-
Vaughan, J.1
Ali, Z.2
Bower, S.3
Bennett, P.4
Chard, T.5
Moore, G.6
-
19
-
-
0024421774
-
The European collaborative study on mosaicism in chorionic villus sampling: Data from 1986 to 1987
-
Vejerslev LO, Mikkelsen M (1989): The European collaborative study on mosaicism in chorionic villus sampling: Data from 1986 to 1987. Prenat Diagn 9:575-588.
-
(1989)
Prenat Diagn
, vol.9
, pp. 575-588
-
-
Vejerslev, L.O.1
Mikkelsen, M.2
-
20
-
-
0029797559
-
Maternal uniparental disomy for chromosome 2 in association with confined placental mosaicism for trisomy 2 and severe intrauterine growth retardation
-
Webb AL, Sturgiss S, Warwicker P, Robson SC, Goodship JA, Wolstenholme J (1996): Maternal uniparental disomy for chromosome 2 in association with confined placental mosaicism for trisomy 2 and severe intrauterine growth retardation. Prenat Diagn 16:958-962.
-
(1996)
Prenat Diagn
, vol.16
, pp. 958-962
-
-
Webb, A.L.1
Sturgiss, S.2
Warwicker, P.3
Robson, S.C.4
Goodship, J.A.5
Wolstenholme, J.6
-
21
-
-
0028925188
-
An audit of trisomy 16 in man
-
Review article
-
Wolstenholme J (1995): An audit of trisomy 16 in man. (Review article). Prenat Diagn 15:109-121.
-
(1995)
Prenat Diagn
, vol.15
, pp. 109-121
-
-
Wolstenholme, J.1
-
22
-
-
0029950129
-
Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16, and 22: Their incidence, likely origins, and mechanisms for cell lineage compartmentalization
-
Wolstenholme J (1996): 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)
Prenat Diagn
, vol.16
, pp. 511-524
-
-
Wolstenholme, J.1
|