Levilliers J - Search Results

1

Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232.

Meitinger T, Heye B, Petit C, Levilliers J, Golla A, Moraine C, Dalla Piccola B, Sippell WG, Murken J, Ballabio A. Meitinger T, et al. Among authors: levilliers j. Am J Hum Genet. 1990 Oct;47(4):664-9. Am J Hum Genet. 1990. PMID: 1977309 Free PMC article.

2

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. Among authors: levilliers j. Hum Genet. 1990 Jul;85(2):247-50. doi: 10.1007/BF00193206. Hum Genet. 1990. PMID: 2370057

3

Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome.

Hardelin JP, Levilliers J, Blanchard S, Carel JC, Leutenegger M, Pinard-Bertelletto JP, Bouloux P, Petit C. Hardelin JP, et al. Among authors: levilliers j. Hum Mol Genet. 1993 Apr;2(4):373-7. doi: 10.1093/hmg/2.4.373. Hum Mol Genet. 1993. PMID: 8504298

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. Among authors: levilliers j. 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

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: levilliers j. Hum Mol Genet. 1994 Dec;3(12):2219-22. doi: 10.1093/hmg/3.12.2219. Hum Mol Genet. 1994. PMID: 7881423

6

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. Among authors: levilliers j. Genomics. 1990 Apr;6(4):651-8. doi: 10.1016/0888-7543(90)90500-t. Genomics. 1990. PMID: 2341154

7

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

Petit C, Levilliers J, Weissenbach J. Petit C, et al. Among authors: levilliers j. 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

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: levilliers j. Genomics. 1995 Mar 20;26(2):229-38. doi: 10.1016/0888-7543(95)80205-z. Genomics. 1995. PMID: 7601447

9

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: levilliers j. Nat Genet. 1994 Jan;6(1):24-8. doi: 10.1038/ng0194-24. Nat Genet. 1994. PMID: 8136828

10

A 45,X male with an X;Y translocation: implications for the mapping of the genes responsible for Turner syndrome and X-linked chondrodysplasia punctata.

Weil D, Portnoï MF, Levilliers J, Wang I, Mathieu M, Taillemite JL, Meier M, Boudailliez B, Petit C. Weil D, et al. Among authors: levilliers j. Hum Mol Genet. 1993 Nov;2(11):1853-6. doi: 10.1093/hmg/2.11.1853. Hum Mol Genet. 1993. PMID: 8281147

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