Lapierre JM - Search Results

1

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: lapierre jm. Clin Genet. 2002 Feb;61(2):135-8. doi: 10.1034/j.1399-0004.2002.610208.x. Clin Genet. 2002. PMID: 11940088

2

Comparative genomic hybridization: technical development and cytogenetic aspects for routine use in clinical laboratories.

Lapierre JM, Cacheux V, Da Silva F, Collot N, Hervy N, Wiss J, Tachdjian G. Lapierre JM, et al. Ann Genet. 1998;41(1):56-62. Ann Genet. 1998. PMID: 9599653

3

Identification and characterization of a de novo partial trisomy 10p by comparative genomic hybridization (CGH).

Benzacken B, Lapierre JM, Siffroi JP, Chalvon A, Tachdjian G. Benzacken B, et al. Among authors: lapierre jm. Clin Genet. 1998 Oct;54(4):334-40. doi: 10.1034/j.1399-0004.1998.5440412.x. Clin Genet. 1998. PMID: 9831346

4

Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalities.

Lapierre JM, Cacheux V, Collot N, Da Silva F, Hervy N, Rivet D, Romana S, Wiss J, Benzaken B, Aurias A, Tachdjian G. Lapierre JM, et al. Ann Genet. 1998;41(3):133-40. Ann Genet. 1998. PMID: 9833066

5

De novo inverted duplication 9p21pter involving telomeric repeated sequences.

Sanlaville D, Baumann C, Lapierre JM, Romana S, Collot N, Cacheux V, Turleau C, Tachdjian G. Sanlaville D, et al. Among authors: lapierre jm. Am J Med Genet. 1999 Mar 12;83(2):125-31. doi: 10.1002/(sici)1096-8628(19990312)83:2<125::aid-ajmg8>3.0.co;2-0. Am J Med Genet. 1999. PMID: 10190483 Review.

6

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: lapierre jm. Am J Med Genet. 2000 Nov 13;95(2):164-8. Am J Med Genet. 2000. PMID: 11078569

7

[Value of molecular cytogenetics in pre- and postnatal diagnostic of chromosome abnormalities].

Romana SP, Gosset P, Elghezal H, Le Lorc'h M, Ozilou C, Lapierre JM, Sanlaville D, Brisset S, Turleau C, Vekemans M. Romana SP, et al. Among authors: lapierre jm. J Gynecol Obstet Biol Reprod (Paris). 2001 Feb;30(1 Suppl):75-9. J Gynecol Obstet Biol Reprod (Paris). 2001. PMID: 11240520 Free article. Review. French. No abstract available.

8

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: lapierre jm. Clin Genet. 2001 Sep;60(3):212-9. doi: 10.1034/j.1399-0004.2001.600307.x. Clin Genet. 2001. PMID: 11595023

9

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: lapierre jm. Am J Med Genet. 2001 Dec 1;104(3):204-8. Am J Med Genet. 2001. PMID: 11754045 Review.

10

Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype.

Faivre L, Cormier-Daire V, Lapierre JM, Colleaux L, Jacquemont S, Geneviéve D, Saunier P, Munnich A, Turleau C, Romana S, Prieur M, De Blois MC, Vekemans M. Faivre L, et al. Among authors: lapierre jm. J Med Genet. 2002 Aug;39(8):594-6. doi: 10.1136/jmg.39.8.594. J Med Genet. 2002. PMID: 12161602 Free PMC article. No abstract available.

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