Bruyere H - Search Results

1

Familial cryptic translocation (2;17) ascertained through recurrent spontaneous abortions.

Bruyere H, Rajcan-Separovic E, Doyle J, Pantzar T, Langlois S. Bruyere H, et al. Am J Med Genet A. 2003 Dec 15;123A(3):285-9. doi: 10.1002/ajmg.a.20228. Am J Med Genet A. 2003. PMID: 14608651

2

Molecular cytogenetics in reproductive pathology.

Bruyère H, Rajcan-Separovic E, Kalousek DK. Bruyère H, et al. Methods Mol Biol. 2002;204:299-307. doi: 10.1385/1-59259-300-3:299. Methods Mol Biol. 2002. PMID: 12397806

3

An association between skewed X-chromosome inactivation and abnormal outcome in mosaic trisomy 16 confined predominantly to the placenta.

Peñaherrera MS, Barrett IJ, Brown CJ, Langlois S, Yong SL, Lewis S, Bruyère H, Howard-Peebles PN, Kalousek DK, Robinson WP. Peñaherrera MS, et al. Among authors: bruyere h. Clin Genet. 2000 Dec;58(6):436-46. doi: 10.1034/j.1399-0004.2000.580603.x. Clin Genet. 2000. PMID: 11149612

4

Risk of mosaicism and uniparental disomy associated with the prenatal diagnosis of a non-homologous Robertsonian translocation carrier.

Bruyère H, Wilson RD, Langlois S. Bruyère H, et al. Fetal Diagn Ther. 2004 Sep-Oct;19(5):399-403. doi: 10.1159/000078991. Fetal Diagn Ther. 2004. PMID: 15305095 Review.

5

V37I connexin 26 allele in patients with sensorineural hearing loss: evidence of its pathogenicity.

Huculak C, Bruyere H, Nelson TN, Kozak FK, Langlois S. Huculak C, et al. Among authors: bruyere h. Am J Med Genet A. 2006 Nov 15;140(22):2394-400. doi: 10.1002/ajmg.a.31486. Am J Med Genet A. 2006. PMID: 17036313

6

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. Clin Genet. 1999 Mar;55(3):173-81. doi: 10.1034/j.1399-0004.1999.550305.x. Clin Genet. 1999. PMID: 10334471

7

Origin of amnion and implications for evaluation of the fetal genotype in cases of mosaicism.

Robinson WP, McFadden DE, Barrett IJ, Kuchinka B, Peñaherrera MS, Bruyère H, Best RG, Pedreira DA, Langlois S, Kalousek DK. Robinson WP, et al. Among authors: bruyere h. Prenat Diagn. 2002 Dec;22(12):1076-85. doi: 10.1002/pd.483. Prenat Diagn. 2002. PMID: 12454962

8

Philadelphia-negative clonal hematopoiesis following imatinib therapy in patients with chronic myeloid leukemia: a report of nine cases and analysis of predictive factors.

Lin Y, Bruyère H, Horsman DE, Pantzar T, Barnett MJ, Hogge DE, Nevill TJ, Nantel SH, Sutherland HJ, Toze CL, Shepherd JD, Lavoie JC, Song KW, Smith CA, Forrest DL. Lin Y, et al. Among authors: bruyere h. Cancer Genet Cytogenet. 2006 Oct 1;170(1):16-23. doi: 10.1016/j.cancergencyto.2006.04.012. Cancer Genet Cytogenet. 2006. PMID: 16965950

9

Isodicentric Yp: prenatal diagnosis and outcome in 12 cases.

Bruyère H, Speevak MD, Winsor EJ, de Fréminville B, Farrell SA, McGowan-Jordan J, McGillivray B, Chitayat D, McFadden D, Adouard V, Terespolsky D, Prieur F, Pantzar T, Hrynchak M. Bruyère H, et al. Prenat Diagn. 2006 Apr;26(4):324-9. doi: 10.1002/pd.1406. Prenat Diagn. 2006. PMID: 16521154 Review.

10

Increasing evidence for a new X-linked mental retardation/epilepsy gene localized to Xp21.3-Xp22.1.

Bruyère H, Lewis ME, Wood S, MacLeod P, Langlois S. Bruyère H, et al. Am J Med Genet. 1999 Oct 8;86(4):401. Am J Med Genet. 1999. PMID: 10494100 No abstract available.

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