Langlois S - Search Results

1

Clinical and molecular findings in two patients with russell-silver syndrome and UPD7: comparison with non-UPD7 cases.

Bernard LE, Peñaherrera MS, Van Allen MI, Wang MS, Yong SL, Gareis F, Langlois S, Robinson WP. Bernard LE, et al. Among authors: langlois s. Am J Med Genet. 1999 Nov 26;87(3):230-6. Am J Med Genet. 1999. PMID: 10564876

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

Characterization of six partial deletions in the low-density-lipoprotein (LDL) receptor gene causing familial hypercholesterolemia (FH).

Langlois S, Kastelein JJ, Hayden MR. Langlois S, et al. Am J Hum Genet. 1988 Jul;43(1):60-8. Am J Hum Genet. 1988. PMID: 2837085 Free PMC article.

4

A polymorphic DNA marker that represents a conserved expressed sequence in the region of the Huntington disease gene.

Hayden MR, Hewitt J, Wasmuth JJ, Kastelein JJ, Langlois S, Conneally M, Haines J, Smith B, Hilbert C, Allard D. Hayden MR, et al. Among authors: langlois s. Am J Hum Genet. 1988 Jan;42(1):125-31. Am J Hum Genet. 1988. PMID: 2892395 Free PMC article.

5

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

6

Parental origin of triploidy in human fetuses: evidence for genomic imprinting.

McFadden DE, Kwong LC, Yam IY, Langlois S. McFadden DE, et al. Among authors: langlois s. Hum Genet. 1993 Nov;92(5):465-9. doi: 10.1007/BF00216452. Hum Genet. 1993. PMID: 7902318

7

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

8

Non-invasive prenatal fetal testing by analysis of maternal blood.

Langlois S, Wilson RD. Langlois S, et al. Clin Invest Med. 1993 Oct;16(5):333-8. Clin Invest Med. 1993. PMID: 8261686

9

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.

10

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.

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