Robinson WP - Search Results

1

Analysis of nine pregnancies with confined placental mosaicism for trisomy 2.

Shaffer LG, Langlois S, McCaskill C, Main DM, Robinson WP, Barrett IJ, Kalousek DK. Shaffer LG, et al. Among authors: robinson wp. Prenat Diagn. 1996 Oct;16(10):899-905. doi: 10.1002/(SICI)1097-0223(199610)16:10<899::AID-PD960>3.0.CO;2-M. Prenat Diagn. 1996. PMID: 8938058

2

Increased parental ages and uniparental disomy 15: a paternal age effect?

Robinson WP, Lorda-Sanchez I, Malcolm S, Langlois S, Schuffenhauer S, Knoblauch H, Horsthemke B, Schinzel AA. Robinson WP, et al. Eur J Hum Genet. 1993;1(4):280-6. doi: 10.1159/000472425. Eur J Hum Genet. 1993. PMID: 8081941

3

Parental origin of the supernumerary chromosome in trisomy 18.

Ya-gang X, Robinson WP, Spiegel R, Binkert F, Ruefenacht U, Schinzel AA. Ya-gang X, et al. Among authors: robinson wp. Clin Genet. 1993 Aug;44(2):57-61. doi: 10.1111/j.1399-0004.1993.tb03847.x. Clin Genet. 1993. PMID: 8275560

4

Nondisjunction of chromosome 15: origin and recombination.

Robinson WP, Bernasconi F, Mutirangura A, Ledbetter DH, Langlois S, Malcolm S, Morris MA, Schinzel AA. Robinson WP, et al. Am J Hum Genet. 1993 Sep;53(3):740-51. Am J Hum Genet. 1993. PMID: 8352279 Free PMC article.

5

Molecular studies of translocations and trisomy involving chromosome 13.

Robinson WP, Bernasconi F, Dutly F, Lefort G, Romain DR, Binkert F, Schinzel AA. Robinson WP, et al. Am J Med Genet. 1996 Jan 11;61(2):158-63. doi: 10.1002/(SICI)1096-8628(19960111)61:2<158::AID-AJMG11>3.0.CO;2-T. Am J Med Genet. 1996. PMID: 8669444

6

Complete paternal isodisomy for chromosome 8 unmasked by lipoprotein lipase deficiency.

Benlian P, Foubert L, Gagné E, Bernard L, De Gennes JL, Langlois S, Robinson W, Hayden M. Benlian P, et al. Am J Hum Genet. 1996 Aug;59(2):431-6. Am J Hum Genet. 1996. PMID: 8755931 Free PMC article.

7

Mosaicism most likely accounts for extended survival of trisomy 22.

Robinson WP, Kalousek DK. Robinson WP, et al. Am J Med Genet. 1996 Mar 1;62(1):100-1. doi: 10.1002/(SICI)1096-8628(19960301)62:1<100::AID-AJMG21>3.0.CO;2-V. Am J Med Genet. 1996. PMID: 8779317 No abstract available.

8

Cytogenetic and age-dependent risk factors associated with uniparental disomy 15.

Robinson WP, Langlois S, Schuffenhauer S, Horsthemke B, Michaelis RC, Christian S, Ledbetter DH, Schinzel A. Robinson WP, et al. Prenat Diagn. 1996 Sep;16(9):837-44. doi: 10.1002/(SICI)1097-0223(199609)16:9<837::AID-PD956>3.0.CO;2-7. Prenat Diagn. 1996. PMID: 8905898

9

Comparison of phenotype in uniparental disomy and deletion Prader-Willi syndrome: sex specific differences.

Mitchell J, Schinzel A, Langlois S, Gillessen-Kaesbach G, Schuffenhauer S, Michaelis R, Abeliovich D, Lerer I, Christian S, Guitart M, McFadden DE, Robinson WP. Mitchell J, et al. Among authors: robinson wp. Am J Med Genet. 1996 Oct 16;65(2):133-6. doi: 10.1002/(SICI)1096-8628(19961016)65:2<133::AID-AJMG10>3.0.CO;2-R. Am J Med Genet. 1996. PMID: 8911605

10

Trisomy 7 CVS mosaicism: pregnancy outcome, placental and DNA analysis in 14 cases.

Kalousek DK, Langlois S, Robinson WP, Telenius A, Bernard L, Barrett IJ, Howard-Peebles PN, Wilson RD. Kalousek DK, et al. Among authors: robinson wp. Am J Med Genet. 1996 Nov 11;65(4):348-52. doi: 10.1002/(SICI)1096-8628(19961111)65:4<348::AID-AJMG19>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8923948

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