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M Leibovici

Showing results (61-70 of 65) with videos related to

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The International Journal of Developmental Biology|March 1, 1990
Genes and mechanisms involved in early embryonic development in Xenopus laevisM Méchali, G Almouzni, Y Andéol, et al.
Nature Genetics|February 1, 1997
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndromeN Neyroud, F Tesson, I Denjoy, et al.
Nature Genetics|September 6, 2000
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1CE Verpy, M Leibovici, I Zwaenepoel, et al.
Nature Genetics|November 1, 2001
Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locusE Verpy, S Masmoudi, I Zwaenepoel, et al.
Nature Genetics|February 1, 1997
A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene familyS Abdelhak, V Kalatzis, R Heilig, et al.
Pageof 7

Showing results (61-70 of 65) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 65 results.
The International Journal of Developmental Biology|March 1, 1990
Genes and mechanisms involved in early embryonic development in Xenopus laevisM Méchali, G Almouzni, Y Andéol, et al.
Nature Genetics|February 1, 1997
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndromeN Neyroud, F Tesson, I Denjoy, et al.
Nature Genetics|September 6, 2000
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1CE Verpy, M Leibovici, I Zwaenepoel, et al.
Nature Genetics|November 1, 2001
Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locusE Verpy, S Masmoudi, I Zwaenepoel, et al.
Nature Genetics|February 1, 1997
A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene familyS Abdelhak, V Kalatzis, R Heilig, et al.
Pageof 7