Lemyre E - Search Results

1

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

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

Prevalence of congenital anomalies at birth among offspring of women at risk for a genetic disorder and with a normal second-trimester ultrasound.

Lemyre E, Infante-Rivard C, Dallaire L. Lemyre E, et al. Teratology. 1999 Oct;60(4):240-4. doi: 10.1002/(SICI)1096-9926(199910)60:4<240::AID-TERA8>3.0.CO;2-T. Teratology. 1999. PMID: 10508977

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

Phenotype of a patient with pure partial trisomy 2p(p23-->pter).

Al-Saffar M, Lemyre E, Koenekoop R, Duncan AM, Der Kaloustian VM. Al-Saffar M, et al. Among authors: lemyre e. Am J Med Genet. 2000 Oct 23;94(5):428-32. doi: 10.1002/1096-8628(20001023)94:5<428::aid-ajmg16>3.0.co;2-m. Am J Med Genet. 2000. PMID: 11050631 Review.

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

Complex mosaicism in sex reversed SRY+ male twins.

DesGroseilliers M, Fortin F, Lemyre E, Lemieux N. DesGroseilliers M, et al. Among authors: lemyre e. Cytogenet Genome Res. 2006;112(1-2):176-9. doi: 10.1159/000087532. Cytogenet Genome Res. 2006. PMID: 16276109

9

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

10

Familial deletion 18p syndrome: case report.

Maranda B, Lemieux N, Lemyre E. Maranda B, et al. Among authors: lemyre e. BMC Med Genet. 2006 Jul 14;7:60. doi: 10.1186/1471-2350-7-60. BMC Med Genet. 2006. PMID: 16842614 Free PMC article.

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