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Jan M Wit

Showing results (191-200 of 216) with videos related to

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American Journal of Human Genetics|July 24, 2018
Bi-allelic Loss-of-Function Mutations in the NPR-C Receptor Result in Enhanced Growth and Connective Tissue AbnormalitiesEveline Boudin, Tjeerd R de Jong, Tim C R Prickett, et al.
American Journal of Medical Genetics. Part A|November 16, 2022
Growth charts for Marfan syndrome in the Netherlands and analysis of genotype-phenotype relationshipsPeter Lauffer, Gerard Pals, Aeilko H Zwinderman, et al.
Endocrine-Related Cancer|December 21, 2014
Is IGSF1 involved in human pituitary tumor formation?Fabio R Faucz, Anelia D Horvath, Monalisa F Azevedo, et al.
The Journal of Clinical Endocrinology and Metabolism|September 24, 2013
An activating mutation in the kinase homology domain of the natriuretic peptide receptor-2 causes extremely tall stature without skeletal deformitiesSabine E Hannema, Hermine A van Duyvenvoorde, Thomas Premsler, et al.
Hormone Research|September 29, 2004
Genotype-phenotype correlation in patients suspected of having Sotos syndromeLonneke de Boer, Sarina G Kant, Marcel Karperien, et al.
European Journal of Human Genetics : EJHG|September 26, 2013
Copy number variants in patients with short statureHermine A van Duyvenvoorde, Julian C Lui, Sarina G Kant, et al.
Pediatric Endocrinology Reviews : PER|May 13, 2015
"Proceedings of the 22nd Aschauer Soiree on Growth and Health Screening", held at Altenhof, Germany, November 15th, 2014Michael Hermanussen, Anna Anisimova, Christian Abmann, et al.
Pediatrics|September 4, 2007
Functional outcomes and participation in young adulthood for very preterm and very low birth weight infants: the Dutch Project on Preterm and Small for Gestational Age Infants at 19 years of ageElysée T M Hille, Nynke Weisglas-Kuperus, J B van Goudoever, et al.
European Journal of Endocrinology|October 19, 2012
Long-term effects of previous oxandrolone treatment in adult women with Turner syndromeKim Freriks, Theo C J Sas, Maaike A F Traas, et al.
The Journal of Clinical Endocrinology and Metabolism|September 8, 2016
Mutations in TBL1X Are Associated With Central HypothyroidismCharlotte A Heinen, Monique Losekoot, Yu Sun, et al.
Pageof 22

Showing results (191-200 of 216) with videos related to

Sort By:
Pageof 22
American Journal of Human Genetics|July 24, 2018
Bi-allelic Loss-of-Function Mutations in the NPR-C Receptor Result in Enhanced Growth and Connective Tissue AbnormalitiesEveline Boudin, Tjeerd R de Jong, Tim C R Prickett, et al.
American Journal of Medical Genetics. Part A|November 16, 2022
Growth charts for Marfan syndrome in the Netherlands and analysis of genotype-phenotype relationshipsPeter Lauffer, Gerard Pals, Aeilko H Zwinderman, et al.
Endocrine-Related Cancer|December 21, 2014
Is IGSF1 involved in human pituitary tumor formation?Fabio R Faucz, Anelia D Horvath, Monalisa F Azevedo, et al.
The Journal of Clinical Endocrinology and Metabolism|September 24, 2013
An activating mutation in the kinase homology domain of the natriuretic peptide receptor-2 causes extremely tall stature without skeletal deformitiesSabine E Hannema, Hermine A van Duyvenvoorde, Thomas Premsler, et al.
Hormone Research|September 29, 2004
Genotype-phenotype correlation in patients suspected of having Sotos syndromeLonneke de Boer, Sarina G Kant, Marcel Karperien, et al.
European Journal of Human Genetics : EJHG|September 26, 2013
Copy number variants in patients with short statureHermine A van Duyvenvoorde, Julian C Lui, Sarina G Kant, et al.
Pediatric Endocrinology Reviews : PER|May 13, 2015
"Proceedings of the 22nd Aschauer Soiree on Growth and Health Screening", held at Altenhof, Germany, November 15th, 2014Michael Hermanussen, Anna Anisimova, Christian Abmann, et al.
Pediatrics|September 4, 2007
Functional outcomes and participation in young adulthood for very preterm and very low birth weight infants: the Dutch Project on Preterm and Small for Gestational Age Infants at 19 years of ageElysée T M Hille, Nynke Weisglas-Kuperus, J B van Goudoever, et al.
European Journal of Endocrinology|October 19, 2012
Long-term effects of previous oxandrolone treatment in adult women with Turner syndromeKim Freriks, Theo C J Sas, Maaike A F Traas, et al.
The Journal of Clinical Endocrinology and Metabolism|September 8, 2016
Mutations in TBL1X Are Associated With Central HypothyroidismCharlotte A Heinen, Monique Losekoot, Yu Sun, et al.
Pageof 22