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Daniel L Metzger

Showing results (51-60 of 55) with videos related to

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Pediatrics|October 8, 2021
Transgender Youth Referred to Clinics for Gender-Affirming Medical Care in CanadaGreta R Bauer, Danièle Pacaud, Robert Couch, et al.
The Journal of Clinical Endocrinology and Metabolism|May 5, 2005
Autosomal dominant resistance to thyrotropin as a distinct entity in five multigenerational kindreds: clinical characterization and exclusion of candidate lociHelmut Grasberger, Aviva Mimouni-Bloch, Marie-Christine Vantyghem, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 12, 2006
Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadismNelly Pitteloud, James S Acierno, Astrid Meysing, et al.
Journal of the American Society of Nephrology : JASN|August 19, 2005
Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemiaKarl P Schlingmann, Martin C Sassen, Stefanie Weber, et al.
The Journal of Clinical Endocrinology and Metabolism|June 30, 2012
When genetic load does not correlate with phenotypic spectrum: lessons from the GnRH receptor (GNRHR)Elena Gianetti, Janet E Hall, Margaret G Au, et al.
Pageof 6

Showing results (51-60 of 55) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 55 results.
Pediatrics|October 8, 2021
Transgender Youth Referred to Clinics for Gender-Affirming Medical Care in CanadaGreta R Bauer, Danièle Pacaud, Robert Couch, et al.
The Journal of Clinical Endocrinology and Metabolism|May 5, 2005
Autosomal dominant resistance to thyrotropin as a distinct entity in five multigenerational kindreds: clinical characterization and exclusion of candidate lociHelmut Grasberger, Aviva Mimouni-Bloch, Marie-Christine Vantyghem, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 12, 2006
Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadismNelly Pitteloud, James S Acierno, Astrid Meysing, et al.
Journal of the American Society of Nephrology : JASN|August 19, 2005
Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemiaKarl P Schlingmann, Martin C Sassen, Stefanie Weber, et al.
The Journal of Clinical Endocrinology and Metabolism|June 30, 2012
When genetic load does not correlate with phenotypic spectrum: lessons from the GnRH receptor (GNRHR)Elena Gianetti, Janet E Hall, Margaret G Au, et al.
Pageof 6