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J Levilliers

Showing results (31-40 of 50) with videos related to

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Genomics|August 1, 1993
Characterization of the chicken and quail homologues of the human gene responsible for the X-linked Kallmann syndromeR Legouis, M Cohen-Salmon, I del Castillo, et al.
Advances in Nephrology From the Necker Hospital|January 16, 1999
Molecular approach to the pathogenesis of renal anomalies in Kallmann's syndrome and in the branchio-oto-renal syndromeJ P Hardelin, N Soussi-Yanicostas, J Levilliers, et al.
Genomics|February 18, 1998
Sequence characterization of a newly identified human alpha-tubulin gene (TUBA2)C Dodé, D Weil, J Levilliers, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1993
Xp22.3 deletions in isolated familial Kallmann's syndromeJ P Hardelin, J Levilliers, J Young, et al.
Genomics|April 1, 1993
A human pseudoautosomal gene encodes the ANT3 ADP/ATP translocase and escapes X-inactivationR Slim, J Levilliers, H J Lüdecke, et al.
Human Molecular Genetics|November 1, 1993
A 45,X male with an X;Y translocation: implications for the mapping of the genes responsible for Turner syndrome and X-linked chondrodysplasia punctataD Weil, M F Portnoï, J Levilliers, et al.
Human Molecular Genetics|April 1, 1993
Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndromeJ P Hardelin, J Levilliers, S Blanchard, et al.
Genomics|September 1, 1995
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)P Guilford, C Dodé, F Crozet, et al.
Nature|March 2, 1995
Defective myosin VIIA gene responsible for Usher syndrome type 1BD Weil, S Blanchard, J Kaplan, et al.
American Journal of Medical Genetics|July 1, 1993
No evidence for linkage to the type 1 or type 2 neurofibromatosis loci in Noonan syndrome familiesW F Flintoff, M Bahuau, S Lyonnet, et al.
Pageof 5

Showing results (31-40 of 50) with videos related to

Sort By:
Pageof 5
Genomics|August 1, 1993
Characterization of the chicken and quail homologues of the human gene responsible for the X-linked Kallmann syndromeR Legouis, M Cohen-Salmon, I del Castillo, et al.
Advances in Nephrology From the Necker Hospital|January 16, 1999
Molecular approach to the pathogenesis of renal anomalies in Kallmann's syndrome and in the branchio-oto-renal syndromeJ P Hardelin, N Soussi-Yanicostas, J Levilliers, et al.
Genomics|February 18, 1998
Sequence characterization of a newly identified human alpha-tubulin gene (TUBA2)C Dodé, D Weil, J Levilliers, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1993
Xp22.3 deletions in isolated familial Kallmann's syndromeJ P Hardelin, J Levilliers, J Young, et al.
Genomics|April 1, 1993
A human pseudoautosomal gene encodes the ANT3 ADP/ATP translocase and escapes X-inactivationR Slim, J Levilliers, H J Lüdecke, et al.
Human Molecular Genetics|November 1, 1993
A 45,X male with an X;Y translocation: implications for the mapping of the genes responsible for Turner syndrome and X-linked chondrodysplasia punctataD Weil, M F Portnoï, J Levilliers, et al.
Human Molecular Genetics|April 1, 1993
Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndromeJ P Hardelin, J Levilliers, S Blanchard, et al.
Genomics|September 1, 1995
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)P Guilford, C Dodé, F Crozet, et al.
Nature|March 2, 1995
Defective myosin VIIA gene responsible for Usher syndrome type 1BD Weil, S Blanchard, J Kaplan, et al.
American Journal of Medical Genetics|July 1, 1993
No evidence for linkage to the type 1 or type 2 neurofibromatosis loci in Noonan syndrome familiesW F Flintoff, M Bahuau, S Lyonnet, et al.
Pageof 5