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Svetlana Ten

Showing results (51-60 of 56) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|November 9, 2021
Profile of Daughters and Sisters of Women With Polycystic Ovary Syndrome: The Role of Proband's Glucose ToleranceSoren Harnois-Leblanc, Maria Isabel Hernandez, Ethel Codner, et al.
Fertility and Sterility|May 26, 2009
Complete androgen insensitivity syndrome is frequently due to premature stop codons in exon 1 of the androgen receptor gene: an international collaborative report of 13 new mutationsPascal Philibert, Françoise Audran, Catherine Pienkowski, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 8, 2012
Retinol binding protein 4 is associated with adiposity-related co-morbidity risk factors in childrenRushika Conroy, Yomery Espinal, Ilene Fennoy, et al.
The Journal of Clinical Endocrinology and Metabolism|July 2, 2009
Expanding the spectrum of mutations in GH1 and GHRHR: genetic screening in a large cohort of patients with congenital isolated growth hormone deficiencyKyriaki S Alatzoglou, James P Turton, Daniel Kelberman, et al.
Human Molecular Genetics|July 10, 2012
An ancient founder mutation in PROKR2 impairs human reproductionMagdalena Avbelj Stefanija, Marc Jeanpierre, Gerasimos P Sykiotis, et al.
The Journal of Clinical Endocrinology and Metabolism|September 2, 2011
GnRH-deficient phenotypes in humans and mice with heterozygous variants in KISS1/Kiss1Yee-Ming Chan, Sarabeth Broder-Fingert, Sophia Paraschos, et al.
Pageof 6

Showing results (51-60 of 56) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 56 results.
The Journal of Clinical Endocrinology and Metabolism|November 9, 2021
Profile of Daughters and Sisters of Women With Polycystic Ovary Syndrome: The Role of Proband's Glucose ToleranceSoren Harnois-Leblanc, Maria Isabel Hernandez, Ethel Codner, et al.
Fertility and Sterility|May 26, 2009
Complete androgen insensitivity syndrome is frequently due to premature stop codons in exon 1 of the androgen receptor gene: an international collaborative report of 13 new mutationsPascal Philibert, Françoise Audran, Catherine Pienkowski, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 8, 2012
Retinol binding protein 4 is associated with adiposity-related co-morbidity risk factors in childrenRushika Conroy, Yomery Espinal, Ilene Fennoy, et al.
The Journal of Clinical Endocrinology and Metabolism|July 2, 2009
Expanding the spectrum of mutations in GH1 and GHRHR: genetic screening in a large cohort of patients with congenital isolated growth hormone deficiencyKyriaki S Alatzoglou, James P Turton, Daniel Kelberman, et al.
Human Molecular Genetics|July 10, 2012
An ancient founder mutation in PROKR2 impairs human reproductionMagdalena Avbelj Stefanija, Marc Jeanpierre, Gerasimos P Sykiotis, et al.
The Journal of Clinical Endocrinology and Metabolism|September 2, 2011
GnRH-deficient phenotypes in humans and mice with heterozygous variants in KISS1/Kiss1Yee-Ming Chan, Sarabeth Broder-Fingert, Sophia Paraschos, et al.
Pageof 6