Langlois S - Search Results

1

Transferrin receptor 2 (TfR2) and HFE mutational analysis in non-C282Y iron overload: identification of a novel TfR2 mutation.

Mattman A, Huntsman D, Lockitch G, Langlois S, Buskard N, Ralston D, Butterfield Y, Rodrigues P, Jones S, Porto G, Marra M, De Sousa M, Vatcher G. Mattman A, et al. Among authors: langlois s. Blood. 2002 Aug 1;100(3):1075-7. doi: 10.1182/blood-2002-01-0133. Blood. 2002. PMID: 12130528 Free article.

2

Frequency of fetal cells in sorted subpopulations of nucleated erythroid and CD34+ hematopoietic progenitor cells from maternal peripheral blood.

Little MT, Langlois S, Wilson RD, Lansdorp PM. Little MT, et al. Among authors: langlois s. Blood. 1997 Apr 1;89(7):2347-58. Blood. 1997. PMID: 9116278 Free article.

3

Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation.

Friedman JM, Baross A, Delaney AD, Ally A, Arbour L, Armstrong L, Asano J, Bailey DK, Barber S, Birch P, Brown-John M, Cao M, Chan S, Charest DL, Farnoud N, Fernandes N, Flibotte S, Go A, Gibson WT, Holt RA, Jones SJ, Kennedy GC, Krzywinski M, Langlois S, Li HI, McGillivray BC, Nayar T, Pugh TJ, Rajcan-Separovic E, Schein JE, Schnerch A, Siddiqui A, Van Allen MI, Wilson G, Yong SL, Zahir F, Eydoux P, Marra MA. Friedman JM, et al. Among authors: langlois s. Am J Hum Genet. 2006 Sep;79(3):500-13. doi: 10.1086/507471. Epub 2006 Jul 25. Am J Hum Genet. 2006. PMID: 16909388 Free PMC article.

4

Novel deletions of 14q11.2 associated with developmental delay, cognitive impairment and similar minor anomalies in three children.

Zahir F, Firth HV, Baross A, Delaney AD, Eydoux P, Gibson WT, Langlois S, Martin H, Willatt L, Marra MA, Friedman JM. Zahir F, et al. Among authors: langlois s. J Med Genet. 2007 Sep;44(9):556-61. doi: 10.1136/jmg.2007.050823. Epub 2007 Jun 1. J Med Genet. 2007. PMID: 17545556 Free PMC article.

5

An evaluation of the decision-making process regarding amniocentesis following a screen-positive maternal serum screen result.

Kobelka C, Mattman A, Langlois S. Kobelka C, et al. Among authors: langlois s. Prenat Diagn. 2009 May;29(5):514-9. doi: 10.1002/pd.2235. Prenat Diagn. 2009. PMID: 19242922

6

A novel de novo 1.1 Mb duplication of 17q21.33 associated with cognitive impairment and other anomalies.

Zahir FR, Langlois S, Gall K, Eydoux P, Marra MA, Friedman JM. Zahir FR, et al. Among authors: langlois s. Am J Med Genet A. 2009 Jun;149A(6):1257-62. doi: 10.1002/ajmg.a.32827. Am J Med Genet A. 2009. PMID: 19449402

7

Steroid sulfatase deficiency and contiguous gene deletion syndrome amongst pregnant patients with low serum unconjugated estriols.

Langlois S, Armstrong L, Gall K, Hulait G, Livingston J, Nelson T, Power P, Pugash D, Siciliano D, Steinraths M, Mattman A. Langlois S, et al. Prenat Diagn. 2009 Oct;29(10):966-74. doi: 10.1002/pd.2326. Prenat Diagn. 2009. PMID: 19609942

8

Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardation.

Tucker T, Montpetit A, Chai D, Chan S, Chénier S, Coe BP, Delaney A, Eydoux P, Lam WL, Langlois S, Lemyre E, Marra M, Qian H, Rouleau GA, Vincent D, Michaud JL, Friedman JM. Tucker T, et al. Among authors: langlois s. BMC Med Genomics. 2011 Mar 25;4:25. doi: 10.1186/1755-8794-4-25. BMC Med Genomics. 2011. PMID: 21439053 Free PMC article.

9

Life-history chronicle for a patient with the recently described chromosome 4q21 microdeletion syndrome.

Tsang E, Rupps R, McGillivray B, Eydoux P, Marra M, Arbour L, Langlois S, Friedman JM, Zahir FR. Tsang E, et al. Among authors: langlois s. Am J Med Genet A. 2012 Oct;158A(10):2606-9. doi: 10.1002/ajmg.a.35568. Epub 2012 Aug 17. Am J Med Genet A. 2012. PMID: 22903878

10

Single exon-resolution targeted chromosomal microarray analysis of known and candidate intellectual disability genes.

Tucker T, Zahir FR, Griffith M, Delaney A, Chai D, Tsang E, Lemyre E, Dobrzeniecka S, Marra M, Eydoux P, Langlois S, Hamdan FF, Michaud JL, Friedman JM. Tucker T, et al. Among authors: langlois s. Eur J Hum Genet. 2014 Jun;22(6):792-800. doi: 10.1038/ejhg.2013.248. Epub 2013 Nov 20. Eur J Hum Genet. 2014. PMID: 24253858 Free PMC article.

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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

363 results

Search Page