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J Levilliers

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American Journal of Human Genetics|October 1, 1990
Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232T Meitinger, B Heye, C Petit, et al.
Nucleic Acids Research|October 11, 1991
A dinucleotide repeat polymorphism at the Kallmann locus (Xp22.3)P M Bouloux, J P Hardelin, P Munroe, et al.
Cell|October 18, 1991
The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion moleculesR Legouis, J P Hardelin, J Levilliers, et al.
Human Molecular Genetics|October 1, 1994
A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR geneC Vincent, V Kalatzis, S Compain, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1992
X chromosome-linked Kallmann syndrome: stop mutations validate the candidate geneJ P Hardelin, J Levilliers, I del Castillo, et al.
Genomics|June 1, 1993
Construction of a yeast artificial chromosome contig spanning the pseudoautosomal region and isolation of 25 new sequence-tagged sitesR Slim, D Le Paslier, S Compain, et al.
Journal of Cell Science|July 1, 1996
Initial characterization of anosmin-1, a putative extracellular matrix protein synthesized by definite neuronal cell populations in the central nervous systemN Soussi-Yanicostas, J P Hardelin, M M Arroyo-Jimenez, et al.
Genomics|March 20, 1995
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)I Wang, B Franco, G B Ferrero, et al.
Cell|April 7, 1995
A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathyB Franco, G Meroni, G Parenti, et al.
Human Molecular Genetics|October 23, 1997
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 geneF Denoyelle, D Weil, M A Maw, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
American Journal of Human Genetics|October 1, 1990
Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232T Meitinger, B Heye, C Petit, et al.
Nucleic Acids Research|October 11, 1991
A dinucleotide repeat polymorphism at the Kallmann locus (Xp22.3)P M Bouloux, J P Hardelin, P Munroe, et al.
Cell|October 18, 1991
The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion moleculesR Legouis, J P Hardelin, J Levilliers, et al.
Human Molecular Genetics|October 1, 1994
A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR geneC Vincent, V Kalatzis, S Compain, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1992
X chromosome-linked Kallmann syndrome: stop mutations validate the candidate geneJ P Hardelin, J Levilliers, I del Castillo, et al.
Genomics|June 1, 1993
Construction of a yeast artificial chromosome contig spanning the pseudoautosomal region and isolation of 25 new sequence-tagged sitesR Slim, D Le Paslier, S Compain, et al.
Journal of Cell Science|July 1, 1996
Initial characterization of anosmin-1, a putative extracellular matrix protein synthesized by definite neuronal cell populations in the central nervous systemN Soussi-Yanicostas, J P Hardelin, M M Arroyo-Jimenez, et al.
Genomics|March 20, 1995
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)I Wang, B Franco, G B Ferrero, et al.
Cell|April 7, 1995
A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathyB Franco, G Meroni, G Parenti, et al.
Human Molecular Genetics|October 23, 1997
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 geneF Denoyelle, D Weil, M A Maw, et al.
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