Langlois S - Search Results

1

Methylation profiling in individuals with Russell-Silver syndrome.

Peñaherrera MS, Weindler S, Van Allen MI, Yong SL, Metzger DL, McGillivray B, Boerkoel C, Langlois S, Robinson WP. Peñaherrera MS, et al. Among authors: langlois s. Am J Med Genet A. 2010 Feb;152A(2):347-55. doi: 10.1002/ajmg.a.33204. Am J Med Genet A. 2010. PMID: 20082469

2

Familial 5q11.2----q13.3 segmental duplication cosegregating with multiple anomalies, including schizophrenia.

McGillivray BC, Bassett AS, Langlois S, Pantzar T, Wood S. McGillivray BC, et al. Among authors: langlois s. Am J Med Genet. 1990 Jan;35(1):10-3. doi: 10.1002/ajmg.1320350103. Am J Med Genet. 1990. PMID: 1967903 Free PMC article.

3

Interstitial 7q deletion [46,XX,del(7)(pter----q21.1::q22----qter)] and the location of genes for beta-glucuronidase and cystic fibrosis.

Chitayat D, McGillivray BC, Wood S, Kalousek DK, Langlois S, Applegarth DA. Chitayat D, et al. Among authors: langlois s. Am J Med Genet. 1988 Nov;31(3):655-61. doi: 10.1002/ajmg.1320310321. Am J Med Genet. 1988. PMID: 3228144

4

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. Among authors: langlois s. Eur J Hum Genet. 1993;1(4):280-6. doi: 10.1159/000472425. Eur J Hum Genet. 1993. PMID: 8081941

5

Evidence for multi-site closure of the neural tube in humans.

Van Allen MI, Kalousek DK, Chernoff GF, Juriloff D, Harris M, McGillivray BC, Yong SL, Langlois S, MacLeod PM, Chitayat D, et al. Van Allen MI, et al. Among authors: langlois s. Am J Med Genet. 1993 Oct 1;47(5):723-43. doi: 10.1002/ajmg.1320470528. Am J Med Genet. 1993. PMID: 8267004 Review.

6

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. Among authors: langlois s. Am J Hum Genet. 1993 Sep;53(3):740-51. Am J Hum Genet. 1993. PMID: 8352279 Free PMC article.

7

Prenatal and postnatal growth failure associated with maternal heterodisomy for chromosome 7.

Langlois S, Yong SL, Wilson RD, Kwong LC, Kalousek DK. Langlois S, et al. J Med Genet. 1995 Nov;32(11):871-5. doi: 10.1136/jmg.32.11.871. J Med Genet. 1995. PMID: 8592330 Free PMC article. Review.

8

Linkage analysis of two Canadian families segregating for X linked spondyloepiphyseal dysplasia.

Bernard LE, Chitayat D, Weksberg R, Van Allen MI, Langlois S. Bernard LE, et al. Among authors: langlois s. J Med Genet. 1996 May;33(5):432-4. doi: 10.1136/jmg.33.5.432. J Med Genet. 1996. PMID: 8733060 Free PMC article.

9

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. Among authors: langlois s. Am J Hum Genet. 1996 Aug;59(2):431-6. Am J Hum Genet. 1996. PMID: 8755931 Free PMC article.

10

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. Among authors: langlois s. 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

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