Langlois S - Search Results

1

Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization.

Friedman J, Adam S, Arbour L, Armstrong L, Baross A, Birch P, Boerkoel C, Chan S, Chai D, Delaney AD, Flibotte S, Gibson WT, Langlois S, Lemyre E, Li HI, MacLeod P, Mathers J, Michaud JL, McGillivray BC, Patel MS, Qian H, Rouleau GA, Van Allen MI, Yong SL, Zahir FR, Eydoux P, Marra MA. Friedman J, et al. Among authors: langlois s. BMC Genomics. 2009 Nov 16;10:526. doi: 10.1186/1471-2164-10-526. BMC Genomics. 2009. PMID: 19917086 Free PMC article.

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

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.

5

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.

6

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.

7

Renal tubular dysgenesis with calvarial hypoplasia: report of two additional cases and review.

McFadden DE, Pantzar JT, Van Allen MI, Langlois S. McFadden DE, et al. Among authors: langlois s. J Med Genet. 1997 Oct;34(10):846-8. doi: 10.1136/jmg.34.10.846. J Med Genet. 1997. PMID: 9350819 Free PMC article.

8

Linkage of malignant hyperthermia and hyperkalemic periodic paralysis to the adult skeletal muscle sodium channel (SCN4A) gene in a large pedigree.

Moslehi R, Langlois S, Yam I, Friedman JM. Moslehi R, et al. Among authors: langlois s. Am J Med Genet. 1998 Feb 26;76(1):21-7. Am J Med Genet. 1998. PMID: 9508059

9

Thalassemia carrier screening and prenatal diagnosis among the British Columbia (Canada) population of Chinese descent.

Yong KN, Wadsworth D, Langlois S, Yong SL, Wilson RD. Yong KN, et al. Among authors: langlois s. Clin Genet. 1999 Jan;55(1):20-5. doi: 10.1034/j.1399-0004.1999.550104.x. Clin Genet. 1999. PMID: 10066027

10

Confirmation of linkage in X-linked infantile spasms (West syndrome) and refinement of the disease locus to Xp21.3-Xp22.1.

Bruyere H, Lewis S, Wood S, MacLeod PJ, Langlois S. Bruyere H, et al. Among authors: langlois s. Clin Genet. 1999 Mar;55(3):173-81. doi: 10.1034/j.1399-0004.1999.550305.x. Clin Genet. 1999. PMID: 10334471

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

367 results

Search Page

Filters