Vekemans M - Search Results

1

Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature.

Brisset S, Joly G, Ozilou C, Lapierre JM, Gosset P, LeLorc'h M, Raoul O, Turleau C, Vekemans M, Romana SP. Brisset S, et al. Among authors: vekemans m. Am J Med Genet. 2002 Dec 15;113(4):339-45. doi: 10.1002/ajmg.b.10740. Am J Med Genet. 2002. PMID: 12457405 Review.

2

Overgrowth and trisomy 15q26.1-qter including the IGF1 receptor gene: report of two families and review of the literature.

Faivre L, Gosset P, Cormier-Daire V, Odent S, Amiel J, Giurgea I, Nassogne MC, Pasquier L, Munnich A, Romana S, Prieur M, Vekemans M, De Blois MC, Turleau C. Faivre L, et al. Among authors: vekemans m. Eur J Hum Genet. 2002 Nov;10(11):699-706. doi: 10.1038/sj.ejhg.5200879. Eur J Hum Genet. 2002. PMID: 12404101

3

Chromosome 10p11.2-p12.2 duplication: report of a patient and review of the literature.

Mégarbané A, Gosset P, Souraty N, Lapierre JM, Korban R, Zahed L, Samaras L, Vekemans M, Prieur M. Mégarbané A, et al. Among authors: vekemans m. Am J Med Genet. 2001 Dec 1;104(3):204-8. Am J Med Genet. 2001. PMID: 11754045 Review.

4

A CGH study of 27 patients with CHARGE association.

Sanlaville D, Romana SP, Lapierre JM, Amiel J, Genevieve D, Ozilou C, Le Lorch M, Brisset S, Gosset P, Baumann C, Turleau C, Lyonnet S, Vekemans M. Sanlaville D, et al. Among authors: vekemans m. Clin Genet. 2002 Feb;61(2):135-8. doi: 10.1034/j.1399-0004.2002.610208.x. Clin Genet. 2002. PMID: 11940088

5

Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation.

Rio M, Molinari F, Heuertz S, Ozilou C, Gosset P, Raoul O, Cormier-Daire V, Amiel J, Lyonnet S, Le Merrer M, Turleau C, de Blois MC, Prieur M, Romana S, Vekemans M, Munnich A, Colleaux L. Rio M, et al. Among authors: vekemans m. J Med Genet. 2002 Apr;39(4):266-70. doi: 10.1136/jmg.39.4.266. J Med Genet. 2002. PMID: 11950856 Free PMC article.

6

Molecular cytogenetic analysis of five 2q37 deletions: refining the brachydactyly candidate region.

Chaabouni M, Le Merrer M, Raoul O, Prieur M, de Blois MC, Philippe A, Vekemans M, Romana SP. Chaabouni M, et al. Among authors: vekemans m. Eur J Med Genet. 2006 May-Jun;49(3):255-63. doi: 10.1016/j.ejmg.2005.07.001. Epub 2005 Aug 18. Eur J Med Genet. 2006. PMID: 16762827

7

Apparent Sotos syndrome (cerebral gigantism) in a child with trisomy 20p11.2-p12.1 mosaicism.

Faivre L, Viot G, Prieur M, Turleau C, Gosset P, Romana S, Munnich A, Vekemans M, Cormier-Daire V. Faivre L, et al. Among authors: vekemans m. Am J Med Genet. 2000 Apr 10;91(4):273-6. Am J Med Genet. 2000. PMID: 10766982

8

Chromosome 7q22-q31 duplication: report of a new case and review.

Mégarbané A, Gosset P, Souraty N, Lapierre JM, Turleau C, Vekemans M, Loiselet J, Prieur M. Mégarbané A, et al. Among authors: vekemans m. Am J Med Genet. 2000 Nov 13;95(2):164-8. Am J Med Genet. 2000. PMID: 11078569

9

Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotype.

Joly G, Lapierre JM, Ozilou C, Gosset P, Aurias A, de Blois MC, Prieur M, Raoul O, Colleaux L, Munnich A, Romana S, Vekemans M, Turleau C. Joly G, et al. Among authors: vekemans m. Clin Genet. 2001 Sep;60(3):212-9. doi: 10.1034/j.1399-0004.2001.600307.x. Clin Genet. 2001. PMID: 11595023

10

PMX2B, a new candidate gene for Hirschsprung's disease.

Benailly HK, Lapierre JM, Laudier B, Amiel J, Attié T, De Blois MC, Vekemans M, Romana SP. Benailly HK, et al. Among authors: vekemans m. Clin Genet. 2003 Sep;64(3):204-9. doi: 10.1034/j.1399-0004.2003.00105.x. Clin Genet. 2003. PMID: 12919134

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