Petit C - Search Results

1

A gene responsible for a sensorineural nonsyndromic recessive deafness maps to chromosome 2p22-23.

Chaïb H, Place C, Salem N, Chardenoux S, Vincent C, Weissenbach J, El-Zir E, Loiselet J, Petit C. Chaïb H, et al. Among authors: petit c. Hum Mol Genet. 1996 Jan;5(1):155-8. doi: 10.1093/hmg/5.1.155. Hum Mol Genet. 1996. PMID: 8789454

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

Long-range restriction map of the terminal part of the short arm of the human X chromosome.

Petit C, Levilliers J, Weissenbach J. Petit C, et al. Proc Natl Acad Sci U S A. 1990 May;87(10):3680-4. doi: 10.1073/pnas.87.10.3680. Proc Natl Acad Sci U S A. 1990. PMID: 2339111 Free PMC article.

5

Isolation of sequences from Xp22.3 and deletion mapping using sex chromosome rearrangements from human X-Y interchange sex reversals.

Petit C, Levilliers J, Rouyer F, Simmler MC, Herouin E, Weissenbach J. Petit C, et al. Genomics. 1990 Apr;6(4):651-8. doi: 10.1016/0888-7543(90)90500-t. Genomics. 1990. PMID: 2341154

6

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

7

Physical mapping of the human pseudo-autosomal region; comparison with genetic linkage map.

Petit C, Levilliers J, Weissenbach J. Petit C, et al. EMBO J. 1988 Aug;7(8):2369-76. doi: 10.1002/j.1460-2075.1988.tb03081.x. EMBO J. 1988. PMID: 2847915 Free PMC article.

8

An abnormal terminal X-Y interchange accounts for most but not all cases of human XX maleness.

Petit C, de la Chapelle A, Levilliers J, Castillo S, Noël B, Weissenbach J. Petit C, et al. Cell. 1987 Jun 5;49(5):595-602. doi: 10.1016/0092-8674(87)90535-6. Cell. 1987. PMID: 2884038

9

Exchange of terminal portions of X- and Y-chromosomal short arms in human XY females.

Levilliers J, Quack B, Weissenbach J, Petit C. Levilliers J, et al. Among authors: petit c. Proc Natl Acad Sci U S A. 1989 Apr;86(7):2296-300. doi: 10.1073/pnas.86.7.2296. Proc Natl Acad Sci U S A. 1989. PMID: 2928333 Free PMC article.

10

The pseudoautosomal region of the human sex chromosomes.

Rouyer F, Simmler MC, Vergnaud G, Johnsson C, Levilliers J, Petit C, Weissenbach J. Rouyer F, et al. Among authors: petit c. Cold Spring Harb Symp Quant Biol. 1986;51 Pt 1:221-8. doi: 10.1101/sqb.1986.051.01.027. Cold Spring Harb Symp Quant Biol. 1986. PMID: 3472718 No abstract available.

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