Petit C - Search Results

1

An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21.

Mustapha M, Weil D, Chardenoux S, Elias S, El-Zir E, Beckmann JS, Loiselet J, Petit C. Mustapha M, et al. Among authors: petit c. Hum Mol Genet. 1999 Mar;8(3):409-12. doi: 10.1093/hmg/8.3.409. Hum Mol Genet. 1999. PMID: 9949200

2

Structure of the X-linked Kallmann syndrome gene and its homologous pseudogene on the Y chromosome.

del Castillo I, Cohen-Salmon M, Blanchard S, Lutfalla G, Petit C. del Castillo I, et al. Among authors: petit c. Nat Genet. 1992 Dec;2(4):305-10. doi: 10.1038/ng1292-305. Nat Genet. 1992. PMID: 1303284

3

X-linked recessive chondrodysplasia punctata with XY translocation in a stillborn fetus.

Van Maldergem L, Espeel M, Roels F, Petit C, Dacremont G, Wanders RJ, Verloes A, Gillerot Y. Van Maldergem L, et al. Among authors: petit c. Hum Genet. 1991 Oct;87(6):661-4. doi: 10.1007/BF00201721. Hum Genet. 1991. PMID: 1937466

4

An interstitial deletion in Xp22.3 in a family with X-linked recessive chondrodysplasia punctata and short stature.

Petit C, Melki J, Levilliers J, Serville F, Weissenbach J, Maroteaux P. Petit C, et al. Hum Genet. 1990 Jul;85(2):247-50. doi: 10.1007/BF00193206. Hum Genet. 1990. PMID: 2370057

5

Prevalence and molecular analysis of two hot spots for ectopic recombination leading to XX maleness.

Wang I, Weil D, Levilliers J, Affara NA, de la Chapelle A, Petit C. Wang I, et al. Among authors: petit c. Genomics. 1995 Jul 1;28(1):52-8. doi: 10.1006/geno.1995.1105. Genomics. 1995. PMID: 7590747

6

High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1).

Wang I, Franco B, Ferrero GB, Chinault AC, Weissenbach J, Chumakov I, Le Paslier D, Levilliers J, Klink A, Rappold GA, Ballabio A, Petit C. Wang I, et al. Among authors: petit c. Genomics. 1995 Mar 20;26(2):229-38. doi: 10.1016/0888-7543(95)80205-z. Genomics. 1995. PMID: 7601447

7

A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval.

Chaïb H, Lina-Granade G, Guilford P, Plauchu H, Levilliers J, Morgon A, Petit C. Chaïb H, et al. Among authors: petit c. Hum Mol Genet. 1994 Dec;3(12):2219-22. doi: 10.1093/hmg/3.12.2219. Hum Mol Genet. 1994. PMID: 7881423

8

Highly homologous loci on the X and Y chromosomes are hot-spots for ectopic recombinations leading to XX maleness.

Weil D, Wang I, Dietrich A, Poustka A, Weissenbach J, Petit C. Weil D, et al. Among authors: petit c. Nat Genet. 1994 Jul;7(3):414-9. doi: 10.1038/ng0794-414. Nat Genet. 1994. PMID: 7920661

9

A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene.

Guilford P, Ayadi H, Blanchard S, Chaib H, Le Paslier D, Weissenbach J, Drira M, Petit C. Guilford P, et al. Among authors: petit c. Hum Mol Genet. 1994 Jun;3(6):989-93. doi: 10.1093/hmg/3.6.989. Hum Mol Genet. 1994. PMID: 7951250

10

A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.

Guilford P, Ben Arab S, Blanchard S, Levilliers J, Weissenbach J, Belkahia A, Petit C. Guilford P, et al. Among authors: petit c. Nat Genet. 1994 Jan;6(1):24-8. doi: 10.1038/ng0194-24. Nat Genet. 1994. PMID: 8136828

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