Turleau C - Search Results

1

Rett phenotype with X/autosome translocation: possible mapping to the short arm of chromosome X.

Journel H, Melki J, Turleau C, Munnich A, de Grouchy J. Journel H, et al. Among authors: turleau c. Am J Med Genet. 1990 Jan;35(1):142-7. doi: 10.1002/ajmg.1320350130. Am J Med Genet. 1990. PMID: 2301467

2

Parental origin of the X chromosomes in Rett syndrome.

Benedetti L, Munnich A, Melki J, Tardieu M, Turleau C. Benedetti L, et al. Among authors: turleau c. Am J Med Genet. 1992 Sep 1;44(1):121-3. doi: 10.1002/ajmg.1320440131. Am J Med Genet. 1992. PMID: 1355631 No abstract available.

3

Trisomy 18qter and trisomy mapping of chromosome 18.

Turleau C, de Grouchy J. Turleau C, et al. Clin Genet. 1977 Dec;12(6):361-71. doi: 10.1111/j.1399-0004.1977.tb00955.x. Clin Genet. 1977. PMID: 589857 No abstract available.

4

Molecular detection of constitutional deletions in patients with retinoblastoma.

Blanquet V, Créau-Goldberg N, de Grouchy J, Turleau C. Blanquet V, et al. Among authors: turleau c. Am J Med Genet. 1991 Jun 1;39(3):355-61. doi: 10.1002/ajmg.1320390321. Am J Med Genet. 1991. PMID: 1867290

5

Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomalies.

Turleau C, Cabanis MO, Girault D, Ledeist F, Mettey R, Puissant H, Prieur M, de Grouchy J. Turleau C, et al. Am J Med Genet. 1989 Mar;32(3):420-4. doi: 10.1002/ajmg.1320320331. Am J Med Genet. 1989. PMID: 2729362

6

Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma.

Henry I, Jeanpierre M, Couillin P, Barichard F, Serre JL, Journel H, Lamouroux A, Turleau C, de Grouchy J, Junien C. Henry I, et al. Among authors: turleau c. Hum Genet. 1989 Feb;81(3):273-7. doi: 10.1007/BF00279003. Hum Genet. 1989. PMID: 2921038

7

Constitutional karyotypes in retinoblastoma.

Turleau C, De Grouchy J. Turleau C, et al. Ophthalmic Paediatr Genet. 1987 Mar;8(1):11-7. doi: 10.3109/13816818709028509. Ophthalmic Paediatr Genet. 1987. PMID: 3295639 Review.

8

A 45,X male with translocation of euchromatic Y chromosome material.

Turleau C, Chavin-Colin F, de Grouchy J. Turleau C, et al. Hum Genet. 1980;53(3):299-302. doi: 10.1007/BF00287044. Hum Genet. 1980. PMID: 7372332

9

Paracentric inversion of the X chromosome [inv(X)(q12q28)] in familial FG syndrome.

Briault S, Odent S, Lucas J, Le Merrer M, Turleau C, Munnich A, Moraine C. Briault S, et al. Among authors: turleau c. Am J Med Genet. 1999 Sep 10;86(2):112-4. doi: 10.1002/(sici)1096-8628(19990910)86:2<112::aid-ajmg4>3.0.co;2-3. Am J Med Genet. 1999. PMID: 10449643

10

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

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