Lemyre E - Search Results

1

Prenatal detection of subtelomeric rearrangements by multi-subtelomere FISH in a cohort of fetuses with major malformations.

Gignac J, Danis K, Tihy F, Lemyre E. Gignac J, et al. Among authors: lemyre e. Am J Med Genet A. 2006 Dec 15;140(24):2768-75. doi: 10.1002/ajmg.a.31472. Am J Med Genet A. 2006. PMID: 17103433

2

Del(14)(q22.1q23.2) in a patient with anophthalmia and pituitary hypoplasia.

Lemyre E, Lemieux N, Décarie JC, Lambert M. Lemyre E, et al. Am J Med Genet. 1998 May 1;77(2):162-5. Am J Med Genet. 1998. PMID: 9605291 Review.

3

Clinical spectrum of infantile free sialic acid storage disease.

Lemyre E, Russo P, Melançon SB, Gagné R, Potier M, Lambert M. Lemyre E, et al. Am J Med Genet. 1999 Feb 19;82(5):385-91. Am J Med Genet. 1999. PMID: 10069709 Review.

4

De novo dup(X)(q22.1q25) in a girl with an abnormal phenotype.

Tihy F, Lemyre E, Lemieux N, Dallaire L. Tihy F, et al. Among authors: lemyre e. Am J Med Genet. 1999 Dec 3;87(4):302-5. Am J Med Genet. 1999. PMID: 10588834 Review.

5

Supernumerary chromosome inherited from a maternal balanced translocation leading to pure trisomy 9p.

Tihy F, Lemyre E, Dallaire L, Lemieux N. Tihy F, et al. Among authors: lemyre e. Am J Med Genet. 2000 Apr 24;91(5):383-6. doi: 10.1002/(sici)1096-8628(20000424)91:5<383::aid-ajmg12>3.0.co;2-g. Am J Med Genet. 2000. PMID: 10767003

6

Tetrasomy Y by structural rearrangement: clinical report.

DesGroseilliers M, Lemyre E, Dallaire L, Lemieux N. DesGroseilliers M, et al. Among authors: lemyre e. Am J Med Genet. 2002 Sep 1;111(4):401-4. doi: 10.1002/ajmg.10591. Am J Med Genet. 2002. PMID: 12210299

7

Complex chromosome rearrangement and recombinant balanced translocation in a mother and a daughter with the same phenotypic abnormalities.

Tihy F, Lemieux N, Lemyre E. Tihy F, et al. Among authors: lemyre e. Am J Med Genet A. 2005 Jun 15;135(3):317-9. doi: 10.1002/ajmg.a.30697. Am J Med Genet A. 2005. PMID: 15887259

8

Male pseudohermaphroditism and gonadal mosaicism in a 47,XY,+22 fetus.

Beaulieu Bergeron M, Tran-Thanh D, Fournet JC, Lemyre E, Lemieux N, Bouron-Dal Soglio D. Beaulieu Bergeron M, et al. Among authors: lemyre e. Am J Med Genet A. 2006 Aug 15;140(16):1768-72. doi: 10.1002/ajmg.a.31338. Am J Med Genet A. 2006. PMID: 16835917

9

Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype.

D'Amours G, Kibar Z, Mathonnet G, Fetni R, Tihy F, Désilets V, Nizard S, Michaud JL, Lemyre E. D'Amours G, et al. Among authors: lemyre e. Clin Genet. 2012 Feb;81(2):128-41. doi: 10.1111/j.1399-0004.2011.01687.x. Epub 2011 May 16. Clin Genet. 2012. PMID: 21496010

10

Correlation of intercentromeric distance, mosaicism, and sexual phenotype: molecular localization of breakpoints in isodicentric Y chromosomes.

Beaulieu Bergeron M, Brochu P, Lemyre E, Lemieux N. Beaulieu Bergeron M, et al. Among authors: lemyre e. Am J Med Genet A. 2011 Nov;155A(11):2705-12. doi: 10.1002/ajmg.a.34260. Epub 2011 Sep 30. Am J Med Genet A. 2011. PMID: 21964771

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