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J P Hardelin

Showing results (1-10 of 27) with videos related to

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Molecular and Cellular Endocrinology|June 23, 2001
Kallmann syndrome: towards molecular pathogenesisJ P Hardelin
Human Reproduction (Oxford, England)|January 20, 1998
Kallmann's syndromeJ P Hardelin
Annales D'Endocrinologie|April 6, 2010
Clinical genetics of Kallmann syndromeC Dodé, J-P Hardelin
Bailliere'S Clinical Endocrinology and Metabolism|July 1, 1995
A molecular approach to the pathophysiology of the X chromosome-linked Kallmann's syndromeJ P Hardelin, C Petit
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|November 7, 2008
The complex genetics of Kallmann syndrome: KAL1, FGFR1, FGF8, PROKR2, PROK2, et alJ-P Hardelin, C Dodé
Annual Review of Genetics|November 9, 2001
Molecular genetics of hearing lossC Petit, J Levilliers, J P Hardelin
La Revue Du Praticien|September 17, 1999
[Genetic anomalies of the gonadotropic axis]N de Roux, Y Morel, J P Hardelin
Anatomy and Embryology|December 1, 1994
Early expression of the KAL gene during embryonic development of the chickR Legouis, J P Hardelin, C Petit, et al.
Advances in Oto-Rhino-Laryngology|June 27, 2000
Kallmann syndromeJ P Hardelin, N Soussi-Yanicostas, O Ardouin, et al.
The Journal of Biological Chemistry|February 11, 1994
Analysis of a brain-specific isozyme. Expression and chromatin structure of the rat aldolase C gene and transgenesI Makeh, M Thomas, J P Hardelin, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Molecular and Cellular Endocrinology|June 23, 2001
Kallmann syndrome: towards molecular pathogenesisJ P Hardelin
Human Reproduction (Oxford, England)|January 20, 1998
Kallmann's syndromeJ P Hardelin
Annales D'Endocrinologie|April 6, 2010
Clinical genetics of Kallmann syndromeC Dodé, J-P Hardelin
Bailliere'S Clinical Endocrinology and Metabolism|July 1, 1995
A molecular approach to the pathophysiology of the X chromosome-linked Kallmann's syndromeJ P Hardelin, C Petit
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|November 7, 2008
The complex genetics of Kallmann syndrome: KAL1, FGFR1, FGF8, PROKR2, PROK2, et alJ-P Hardelin, C Dodé
Annual Review of Genetics|November 9, 2001
Molecular genetics of hearing lossC Petit, J Levilliers, J P Hardelin
La Revue Du Praticien|September 17, 1999
[Genetic anomalies of the gonadotropic axis]N de Roux, Y Morel, J P Hardelin
Anatomy and Embryology|December 1, 1994
Early expression of the KAL gene during embryonic development of the chickR Legouis, J P Hardelin, C Petit, et al.
Advances in Oto-Rhino-Laryngology|June 27, 2000
Kallmann syndromeJ P Hardelin, N Soussi-Yanicostas, O Ardouin, et al.
The Journal of Biological Chemistry|February 11, 1994
Analysis of a brain-specific isozyme. Expression and chromatin structure of the rat aldolase C gene and transgenesI Makeh, M Thomas, J P Hardelin, et al.
Pageof 3