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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.
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.
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
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. Am J Med Genet. 1999 Dec 3;87(4):302-5. Am J Med Genet. 1999. PMID: 10588834 Review.
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. 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.
Stable non-Robertsonian dicentric chromosomes: four new cases and a review.
Lemyre E, der Kaloustian VM, Duncan AM. Lemyre E, et al. J Med Genet. 2001 Jan;38(1):76-9. doi: 10.1136/jmg.38.1.76. J Med Genet. 2001. PMID: 11335984 Free PMC article. Review. No abstract available.
Prenatal diagnosis and molecular cytogenetics in a case of partial trisomy 14 and monosomy 21.
Lee C, Fowler DJ, Lemyre E, Sandstrom MM, Holmes LB, Morton CC. Lee C, et al. Am J Med Genet. 2001 May 1;100(3):246-50. doi: 10.1002/1096-8628(20010501)100:3<246::aid-ajmg1254>3.0.co;2-n. Am J Med Genet. 2001. PMID: 11343311
Tetrasomy Y by structural rearrangement: clinical report.
DesGroseilliers M, Lemyre E, Dallaire L, Lemieux N. DesGroseilliers M, et al. Am J Med Genet. 2002 Sep 1;111(4):401-4. doi: 10.1002/ajmg.10591. Am J Med Genet. 2002. PMID: 12210299
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