Gosset P - Search Results

1

Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann features.

Fert-Ferrer S, Guichet A, Tantau J, Delezoide AL, Ozilou C, Romana SP, Gosset P, Viot G, Loison S, Moraine C, Morichon-Delvallez N, Turleau C, Vekemans M, Prieur M. Fert-Ferrer S, et al. Among authors: gosset p. Prenat Diagn. 2000 Jun;20(6):511-5. doi: 10.1002/1097-0223(200006)20:6<511::aid-pd849>3.0.co;2-b. Prenat Diagn. 2000. PMID: 10861719

2

Prenatal diagnosis and characterization of an analphoid marker chromosome 16.

Tabet AC, Gosset P, Elghezal H, Fontaine S, Martinovic J, Encha Razavi F, Romana S, Vekemans M, Morichon-Delvallez N. Tabet AC, et al. Among authors: gosset p. Prenat Diagn. 2004 Sep;24(9):733-6. doi: 10.1002/pd.804. Prenat Diagn. 2004. PMID: 15386469

3

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: gosset p. 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.

4

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: gosset p. Eur J Hum Genet. 2002 Nov;10(11):699-706. doi: 10.1038/sj.ejhg.5200879. Eur J Hum Genet. 2002. PMID: 12404101

5

Functional disomy of the Xq28 chromosome region.

Sanlaville D, Prieur M, de Blois MC, Genevieve D, Lapierre JM, Ozilou C, Picq M, Gosset P, Morichon-Delvallez N, Munnich A, Cormier-Daire V, Baujat G, Romana S, Vekemans M, Turleau C. Sanlaville D, et al. Among authors: gosset p. Eur J Hum Genet. 2005 May;13(5):579-85. doi: 10.1038/sj.ejhg.5201384. Eur J Hum Genet. 2005. PMID: 15741994 Review.

6

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: gosset p. Am J Med Genet. 2000 Apr 10;91(4):273-6. Am J Med Genet. 2000. PMID: 10766982

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: gosset p. 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

A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardation.

Colleaux L, Rio M, Heuertz S, Moindrault S, Turleau C, Ozilou C, Gosset P, Raoult O, Lyonnet S, Cormier-Daire V, Amiel J, Le Merrer M, Picq M, de Blois MC, Prieur M, Romana S, Cornelis F, Vekemans M, Munnich A. Colleaux L, et al. Among authors: gosset p. Eur J Hum Genet. 2001 May;9(5):319-27. doi: 10.1038/sj.ejhg.5200591. Eur J Hum Genet. 2001. PMID: 11378819

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

10

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

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