Petit C - Search Results

1

A subtracted cDNA library from the zebrafish (Danio rerio) embryonic inner ear.

Coimbra RS, Weil D, Brottier P, Blanchard S, Levi M, Hardelin JP, Weissenbach J, Petit C. Coimbra RS, et al. Among authors: petit c. Genome Res. 2002 Jun;12(6):1007-11. doi: 10.1101/gr.227502. Genome Res. 2002. PMID: 12045154 Free PMC article.

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

A dinucleotide repeat polymorphism at the Kallmann locus (Xp22.3).

Bouloux PM, Hardelin JP, Munroe P, Kirk JM, Legouis R, Levilliers J, Hazan J, Weissenbach J, Petit C. Bouloux PM, et al. Among authors: petit c. Nucleic Acids Res. 1991 Oct 11;19(19):5453. doi: 10.1093/nar/19.19.5453. Nucleic Acids Res. 1991. PMID: 1923841 Free PMC article.

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

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.

9

Normal and abnormal interchanges between the human X and Y chromosomes.

Weissenbach J, Levilliers J, Petit C, Rouyer F, Simmler MC. Weissenbach J, et al. Among authors: petit c. Development. 1987;101 Suppl:67-74. Development. 1987. PMID: 3503725

10

A molecular approach to the pathophysiology of the X chromosome-linked Kallmann's syndrome.

Hardelin JP, Petit C. Hardelin JP, et al. Among authors: petit c. Baillieres Clin Endocrinol Metab. 1995 Jul;9(3):489-507. doi: 10.1016/s0950-351x(95)80553-2. Baillieres Clin Endocrinol Metab. 1995. PMID: 7575329 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,069 results

Search Page

Filters