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J P Hardelin

Showing results (21-30 of 27) with videos related to

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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.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|May 26, 1999
Anosmin-1 is a regionally restricted component of basement membranes and interstitial matrices during organogenesis: implications for the developmental anomalies of X chromosome-linked Kallmann syndromeJ P Hardelin, A K Julliard, B Moniot, 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.
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.
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.
Gene|July 16, 2013
Biallelic nonsense mutations in the otogelin-like gene (OTOGL) in a child affected by mild to moderate hearing impairmentC Bonnet, M Louha, N Loundon, et al.
Nature|April 1, 2026
Dopaminergic mechanisms of dynamical social specializationC Solié, A Nicolson, R Justo, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
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.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|May 26, 1999
Anosmin-1 is a regionally restricted component of basement membranes and interstitial matrices during organogenesis: implications for the developmental anomalies of X chromosome-linked Kallmann syndromeJ P Hardelin, A K Julliard, B Moniot, 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.
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.
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.
Gene|July 16, 2013
Biallelic nonsense mutations in the otogelin-like gene (OTOGL) in a child affected by mild to moderate hearing impairmentC Bonnet, M Louha, N Loundon, et al.
Nature|April 1, 2026
Dopaminergic mechanisms of dynamical social specializationC Solié, A Nicolson, R Justo, et al.
Pageof 3