Turleau C - Search Results

1

Prenatal diagnosis of a satellited non-acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literature.

Faivre L, Morichon-Delvallez N, Viot G, Larget-Piet A, Narcy F, Turleau C, Pinson MP, Dumez Y, Munnich A, Vekemans M. Faivre L, et al. Among authors: turleau c. Prenat Diagn. 1999 Mar;19(3):282-6. Prenat Diagn. 1999. PMID: 10210132 Review.

2

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: turleau c. 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

3

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

4

Prenatal overgrowth and mosaic trisomy 15q25-qter including the IGF1 receptor gene.

Faivre L, Rousseau T, Laurent N, Gosset P, Sanlaville D, Thauvin-Robinet C, Cusin V, Lionnais S, Callier P, Khau Van Kien P, Huet F, Turleau C, Sagot P, Mugneret F. Faivre L, et al. Among authors: turleau c. Prenat Diagn. 2004 May;24(5):393-5. doi: 10.1002/pd.891. Prenat Diagn. 2004. PMID: 15164417

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: turleau c. 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

[New developments in cytogenetics].

Turleau C, Vekemans M. Turleau C, et al. Med Sci (Paris). 2005 Nov;21(11):940-6. doi: 10.1051/medsci/20052111940. Med Sci (Paris). 2005. PMID: 16274645 Free article. Review. French.

7

[Problems posed by genetic diseases: trisomy 21].

Morichon-Delvallez N, Turleau C. Morichon-Delvallez N, et al. Among authors: turleau c. Rev Prat. 2006 Jun 30;56(12):1357-62. Rev Prat. 2006. PMID: 16948227 Review. French. No abstract available.

8

[Trisomy 21: fifty years between medicine and science].

Turleau C, Vekemans M. Turleau C, et al. Med Sci (Paris). 2010 Mar;26(3):267-72. doi: 10.1051/medsci/2010263267. Med Sci (Paris). 2010. PMID: 20346276 Free article. Review. French.

9

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

10

Partial maternal heterodisomy of chromosome 17q25 in a case of severe mental retardation.

Rio M, Ozilou C, Cormier-Daire V, Turleau C, Prieur M, Vekemans M, Chauveau P, Munnich A, Colleaux L. Rio M, et al. Among authors: turleau c. Hum Genet. 2001 Jun;108(6):511-5. doi: 10.1007/s004390100522. Hum Genet. 2001. PMID: 11499677

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