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Martin Zenker

Showing results (31-40 of 338) with videos related to

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Endocrine Connections|May 29, 2026
Maternal methyl-donor supplementation and hypothalamic methylation stabilityThomas Gerhard Brune, Bettina Schloesser, Marianne Volleth, et al.
Archives of Disease in Childhood|March 5, 2022
Noonan syndrome: improving recognition and diagnosisMartin Zenker, Thomas Edouard, Joanne C Blair, et al.
European Journal of Medical Genetics|December 28, 2018
Hypopigmented patches in Roberts/SC phocomelia syndrome occur via aneuploidy susceptibilityAbdullah Sezer, Gulsum Kayhan, Martin Zenker, et al.
Endocrinology and Metabolism Clinics of North America|April 25, 2006
Developmental and metabolic disorders of the pancreasMarkus M Lerch, Martin Zenker, Stefan Turi, et al.
Endocrinology and Metabolism Clinics of North America|April 25, 2006
Genetic basis and pancreatic biology of Johanson-Blizzard syndromeMartin Zenker, Julia Mayerle, André Reis, et al.
Frontiers in Endocrinology|January 23, 2023
Editorial: Endocrine aspects of Noonan syndrome and related syndromesGiorgio Radetti, Thomas Edouard, Laura Mazzanti, et al.
American Journal of Medical Genetics. Part A|April 6, 2006
Genotype-epigenotype-phenotype correlations in females with frontometaphyseal dysplasiaMartin Zenker, Lutz Nährlich, Heinrich Sticht, et al.
American Journal of Medical Genetics. Part A|November 15, 2006
A variable combination of features of Noonan syndrome and neurofibromatosis type I are caused by mutations in the NF1 geneUlrike Hüffmeier, Martin Zenker, Juliane Hoyer, et al.
Acta Dermato-Venereologica|January 17, 2018
A Postzygotic SMO Mutation Caused the Original Case of Happle-Tinschert SyndromeMartin Zenker, Sigrid Tinschert, Ilse Wieland, et al.
Thrombosis Research|September 19, 2012
Bleeding diathesis in Noonan syndrome: is acquired von Willebrand syndrome the clue?Gesa Wiegand, Michael Hofbeck, Martin Zenker, et al.
Pageof 34

Showing results (31-40 of 338) with videos related to

Sort By:
Pageof 34
Endocrine Connections|May 29, 2026
Maternal methyl-donor supplementation and hypothalamic methylation stabilityThomas Gerhard Brune, Bettina Schloesser, Marianne Volleth, et al.
Archives of Disease in Childhood|March 5, 2022
Noonan syndrome: improving recognition and diagnosisMartin Zenker, Thomas Edouard, Joanne C Blair, et al.
European Journal of Medical Genetics|December 28, 2018
Hypopigmented patches in Roberts/SC phocomelia syndrome occur via aneuploidy susceptibilityAbdullah Sezer, Gulsum Kayhan, Martin Zenker, et al.
Endocrinology and Metabolism Clinics of North America|April 25, 2006
Developmental and metabolic disorders of the pancreasMarkus M Lerch, Martin Zenker, Stefan Turi, et al.
Endocrinology and Metabolism Clinics of North America|April 25, 2006
Genetic basis and pancreatic biology of Johanson-Blizzard syndromeMartin Zenker, Julia Mayerle, André Reis, et al.
Frontiers in Endocrinology|January 23, 2023
Editorial: Endocrine aspects of Noonan syndrome and related syndromesGiorgio Radetti, Thomas Edouard, Laura Mazzanti, et al.
American Journal of Medical Genetics. Part A|April 6, 2006
Genotype-epigenotype-phenotype correlations in females with frontometaphyseal dysplasiaMartin Zenker, Lutz Nährlich, Heinrich Sticht, et al.
American Journal of Medical Genetics. Part A|November 15, 2006
A variable combination of features of Noonan syndrome and neurofibromatosis type I are caused by mutations in the NF1 geneUlrike Hüffmeier, Martin Zenker, Juliane Hoyer, et al.
Acta Dermato-Venereologica|January 17, 2018
A Postzygotic SMO Mutation Caused the Original Case of Happle-Tinschert SyndromeMartin Zenker, Sigrid Tinschert, Ilse Wieland, et al.
Thrombosis Research|September 19, 2012
Bleeding diathesis in Noonan syndrome: is acquired von Willebrand syndrome the clue?Gesa Wiegand, Michael Hofbeck, Martin Zenker, et al.
Pageof 34