Weil D - Search Results

1

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: weil d. Genomics. 1995 Jul 1;28(1):52-8. doi: 10.1006/geno.1995.1105. Genomics. 1995. PMID: 7590747

2

Human type I procollagen genes are located on different chromosomes.

Huerre C, Junien C, Weil D, Chu ML, Morabito M, Van Cong N, Myers JC, Foubert C, Gross MS, Prockop DJ, Boué A, Kaplan JC, de la Chapelle A, Ramirez F. Huerre C, et al. Among authors: weil d. Proc Natl Acad Sci U S A. 1982 Nov;79(21):6627-30. doi: 10.1073/pnas.79.21.6627. Proc Natl Acad Sci U S A. 1982. PMID: 6292910 Free PMC article.

3

Defective myosin VIIA gene responsible for Usher syndrome type 1B.

Weil D, Blanchard S, Kaplan J, Guilford P, Gibson F, Walsh J, Mburu P, Varela A, Levilliers J, Weston MD, et al. Weil D, et al. Nature. 1995 Mar 2;374(6517):60-1. doi: 10.1038/374060a0. Nature. 1995. PMID: 7870171

4

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. Nat Genet. 1994 Jul;7(3):414-9. doi: 10.1038/ng0794-414. Nat Genet. 1994. PMID: 7920661

5

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. Hum Mol Genet. 1993 Nov;2(11):1853-6. doi: 10.1093/hmg/2.11.1853. Hum Mol Genet. 1993. PMID: 8281147

6

A YAC contig and an EST map in the pericentromeric region of chromosome 13 surrounding the loci for neurosensory nonsyndromic deafness (DFNB1 and DFNA3) and limb-girdle muscular dystrophy type 2C (LGMD2C).

Guilford P, Dodé C, Crozet F, Blanchard S, Chaïb H, Levilliers J, Levi-Acobas F, Weil D, Weissenbach J, Cohen D, et al. Guilford P, et al. Among authors: weil d. Genomics. 1995 Sep 1;29(1):163-9. doi: 10.1006/geno.1995.1227. Genomics. 1995. PMID: 8530067

7

Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia.

Weil D, Levy G, Sahly I, Levi-Acobas F, Blanchard S, El-Amraoui A, Crozet F, Philippe H, Abitbol M, Petit C. Weil D, et al. Proc Natl Acad Sci U S A. 1996 Apr 16;93(8):3232-7. doi: 10.1073/pnas.93.8.3232. Proc Natl Acad Sci U S A. 1996. PMID: 8622919 Free PMC article.

8

Myosin VIIA gene: heterogeneity of the mutations responsible for Usher syndrome type IB.

Lévy G, Levi-Acobas F, Blanchard S, Gerber S, Larget-Piet D, Chenal V, Liu XZ, Newton V, Steel KP, Brown SD, Munnich A, Kaplan J, Petit C, Weil D. Lévy G, et al. Among authors: weil d. Hum Mol Genet. 1997 Jan;6(1):111-6. doi: 10.1093/hmg/6.1.111. Hum Mol Genet. 1997. PMID: 9002678

9

A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family.

Abdelhak S, Kalatzis V, Heilig R, Compain S, Samson D, Vincent C, Weil D, Cruaud C, Sahly I, Leibovici M, Bitner-Glindzicz M, Francis M, Lacombe D, Vigneron J, Charachon R, Boven K, Bedbeder P, Van Regemorter N, Weissenbach J, Petit C. Abdelhak S, et al. Among authors: weil d. Nat Genet. 1997 Feb;15(2):157-64. doi: 10.1038/ng0297-157. Nat Genet. 1997. PMID: 9020840

10

Cloning of the genes encoding two murine and human cochlear unconventional type I myosins.

Crozet F, el Amraoui A, Blanchard S, Lenoir M, Ripoll C, Vago P, Hamel C, Fizames C, Levi-Acobas F, Depétris D, Mattei MG, Weil D, Pujol R, Petit C. Crozet F, et al. Among authors: weil d. Genomics. 1997 Mar 1;40(2):332-41. doi: 10.1006/geno.1996.4526. Genomics. 1997. PMID: 9119401

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