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Jan M Wit

Showing results (211-220 of 216) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|October 20, 2009
Efficacy and safety of long-term continuous growth hormone treatment in children with Prader-Willi syndromeRoderick F A de Lind van Wijngaarden, Elbrich P C Siemensma, Dederieke A M Festen, et al.
Hormone Research in Paediatrics|September 13, 2019
Diagnosis, Genetics, and Therapy of Short Stature in Children: A Growth Hormone Research Society International PerspectivePaulo F Collett-Solberg, Geoffrey Ambler, Philippe F Backeljauw, et al.
The Journal of Clinical Endocrinology and Metabolism|January 9, 2025
Loss-of-Function GHSR Variants Are Associated With Short Stature and Low IGF-ILauren D Punt, Sander Kooijman, Noa J M Mutsters, et al.
American Journal of Human Genetics|December 14, 2020
SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signalingYuh-Charn Lin, Marcello Niceta, Valentina Muto, et al.
Nature Genetics|November 13, 2012
Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargementYu Sun, Beata Bak, Nadia Schoenmakers, et al.
Orphanet Journal of Rare Diseases|April 30, 2013
The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAPSarah M Nikkel, Andrew Dauber, Sonja de Munnik, et al.
Pageof 22

Showing results (211-220 of 216) with videos related to

Sort By:
Pageof 22
You have reached the last page of results.This site can display upto 216 results.
The Journal of Clinical Endocrinology and Metabolism|October 20, 2009
Efficacy and safety of long-term continuous growth hormone treatment in children with Prader-Willi syndromeRoderick F A de Lind van Wijngaarden, Elbrich P C Siemensma, Dederieke A M Festen, et al.
Hormone Research in Paediatrics|September 13, 2019
Diagnosis, Genetics, and Therapy of Short Stature in Children: A Growth Hormone Research Society International PerspectivePaulo F Collett-Solberg, Geoffrey Ambler, Philippe F Backeljauw, et al.
The Journal of Clinical Endocrinology and Metabolism|January 9, 2025
Loss-of-Function GHSR Variants Are Associated With Short Stature and Low IGF-ILauren D Punt, Sander Kooijman, Noa J M Mutsters, et al.
American Journal of Human Genetics|December 14, 2020
SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signalingYuh-Charn Lin, Marcello Niceta, Valentina Muto, et al.
Nature Genetics|November 13, 2012
Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargementYu Sun, Beata Bak, Nadia Schoenmakers, et al.
Orphanet Journal of Rare Diseases|April 30, 2013
The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAPSarah M Nikkel, Andrew Dauber, Sonja de Munnik, et al.
Pageof 22