Langlois S - Search Results

1

Assessment of the Effectiveness of Genetic Counseling by Telephone Compared to a Clinic Visit.

Sangha KK, Dircks A, Langlois S. Sangha KK, et al. Among authors: langlois s. J Genet Couns. 2003 Apr;12(2):171-84. doi: 10.1023/A:1022663324006. J Genet Couns. 2003. PMID: 26140847

2

Duty to re-contact: a study of families at risk for Fragile X.

Bernard LE, McGillivray B, Van Allen MI, Friedman JM, Langlois S. Bernard LE, et al. Among authors: langlois s. J Genet Couns. 1999 Feb;8(1):3-15. doi: 10.1023/a:1022878402764. J Genet Couns. 1999. PMID: 11657178 No abstract available.

3

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

4

The association between preeclampsia and placental trisomy 16 mosaicism.

Yong PJ, Langlois S, von Dadelszen P, Robinson W. Yong PJ, et al. Among authors: langlois s. Prenat Diagn. 2006 Oct;26(10):956-61. doi: 10.1002/pd.1534. Prenat Diagn. 2006. PMID: 16874839

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

Maternal serum screening in triploidy.

McFadden DE, Hulait G, Lockitch G, Langlois S. McFadden DE, et al. Among authors: langlois s. Prenat Diagn. 2002 Dec;22(12):1113-4. doi: 10.1002/pd.477. Prenat Diagn. 2002. PMID: 12454969 No abstract available.

7

Prenatal ultrasound and MRI findings of temporal and occipital lobe dysplasia in a twin with achondroplasia.

Pugash D, Lehman AM, Langlois S. Pugash D, et al. Among authors: langlois s. Ultrasound Obstet Gynecol. 2014 Sep;44(3):365-8. doi: 10.1002/uog.13359. Ultrasound Obstet Gynecol. 2014. PMID: 24616001 Free article.

8

Etiologies and outcomes of prenatally diagnosed hyperechogenic kidneys.

Digby EL, Liauw J, Dionne J, Langlois S, Nikkel SM. Digby EL, et al. Among authors: langlois s. Prenat Diagn. 2021 Mar;41(4):465-477. doi: 10.1002/pd.5883. Epub 2021 Jan 3. Prenat Diagn. 2021. PMID: 33337554

9

Current controversies in prenatal diagnosis 4: pre-conception expanded carrier screening should replace all current prenatal screening for specific single gene disorders.

Langlois S, Benn P, Wilkins-Haug L. Langlois S, et al. Prenat Diagn. 2015 Jan;35(1):23-8. doi: 10.1002/pd.4532. Prenat Diagn. 2015. PMID: 25395388 No abstract available.

10

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.

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