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Gudrun A Rappold

Showing results (1-10 of 77) with videos related to

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Endocrine Journal|September 1, 2024
Celebrating the 100<sup>th</sup> anniversary of the Japan Endocrine Society and international collaborationsGudrun A Rappold
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|September 11, 2024
10 Years of International Albinism Awareness: United Nations celebrate an anniversary and a decade of collective progress, but challenges remainGudrun A Rappold
Nature Reviews. Endocrinology|January 23, 2013
Height matters-from monogenic disorders to normal variationClaudia Durand, Gudrun A Rappold
Molecular Psychiatry|May 29, 2020
Emerging evidence for gene mutations driving both brain and gut dysfunction in autism spectrum disorderBeate Niesler, Gudrun A Rappold
Human Genetics|June 28, 2012
The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disordersClaire Bacon, Gudrun A Rappold
Science in Context|September 1, 2022
Representing vulnerable populations in genetic studies: The case of the RomaVeronika Lipphardt, Gudrun A Rappold, Mihai Surdu
Endocrine Reviews|June 30, 2016
A Track Record on SHOX: From Basic Research to Complex Models and TherapyAntonio Marchini, Tsutomu Ogata, Gudrun A Rappold
Mechanisms of Development|November 7, 2012
The cellular function of srGAP3 and its role in neuronal morphogenesisClaire Bacon, Volker Endris, Gudrun A Rappold
The Journal of Pediatrics|October 18, 2005
All shook up by SHOX deficiencyGudrun A Rappold, Alan Shanske, Paul Saenger
Human Mutation|October 29, 2002
The human SHOX mutation databaseBeate Niesler, Christine Fischer, Gudrun A Rappold
Pageof 8

Showing results (1-10 of 77) with videos related to

Sort By:
Pageof 8
Endocrine Journal|September 1, 2024
Celebrating the 100<sup>th</sup> anniversary of the Japan Endocrine Society and international collaborationsGudrun A Rappold
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|September 11, 2024
10 Years of International Albinism Awareness: United Nations celebrate an anniversary and a decade of collective progress, but challenges remainGudrun A Rappold
Nature Reviews. Endocrinology|January 23, 2013
Height matters-from monogenic disorders to normal variationClaudia Durand, Gudrun A Rappold
Molecular Psychiatry|May 29, 2020
Emerging evidence for gene mutations driving both brain and gut dysfunction in autism spectrum disorderBeate Niesler, Gudrun A Rappold
Human Genetics|June 28, 2012
The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disordersClaire Bacon, Gudrun A Rappold
Science in Context|September 1, 2022
Representing vulnerable populations in genetic studies: The case of the RomaVeronika Lipphardt, Gudrun A Rappold, Mihai Surdu
Endocrine Reviews|June 30, 2016
A Track Record on SHOX: From Basic Research to Complex Models and TherapyAntonio Marchini, Tsutomu Ogata, Gudrun A Rappold
Mechanisms of Development|November 7, 2012
The cellular function of srGAP3 and its role in neuronal morphogenesisClaire Bacon, Volker Endris, Gudrun A Rappold
The Journal of Pediatrics|October 18, 2005
All shook up by SHOX deficiencyGudrun A Rappold, Alan Shanske, Paul Saenger
Human Mutation|October 29, 2002
The human SHOX mutation databaseBeate Niesler, Christine Fischer, Gudrun A Rappold
Pageof 8