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Endocrine Journal
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September 1, 2024
Celebrating the 100<sup>th</sup> anniversary of the Japan Endocrine Society and international collaborations
Gudrun 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 remain
Gudrun A Rappold
Nature Reviews. Endocrinology
|
January 23, 2013
Height matters-from monogenic disorders to normal variation
Claudia Durand, Gudrun A Rappold
Molecular Psychiatry
|
May 29, 2020
Emerging evidence for gene mutations driving both brain and gut dysfunction in autism spectrum disorder
Beate Niesler, Gudrun A Rappold
Human Genetics
|
June 28, 2012
The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders
Claire Bacon, Gudrun A Rappold
Science in Context
|
September 1, 2022
Representing vulnerable populations in genetic studies: The case of the Roma
Veronika Lipphardt, Gudrun A Rappold, Mihai Surdu
Endocrine Reviews
|
June 30, 2016
A Track Record on SHOX: From Basic Research to Complex Models and Therapy
Antonio Marchini, Tsutomu Ogata, Gudrun A Rappold
Mechanisms of Development
|
November 7, 2012
The cellular function of srGAP3 and its role in neuronal morphogenesis
Claire Bacon, Volker Endris, Gudrun A Rappold
The Journal of Pediatrics
|
October 18, 2005
All shook up by SHOX deficiency
Gudrun A Rappold, Alan Shanske, Paul Saenger
Human Mutation
|
October 29, 2002
The human SHOX mutation database
Beate Niesler, Christine Fischer, Gudrun A Rappold
Page
of 8
Search research articles
Search
Showing results (1-10 of 77) with videos related to
Sort By:
Page
of 8
Endocrine Journal
|
September 1, 2024
Celebrating the 100<sup>th</sup> anniversary of the Japan Endocrine Society and international collaborations
Gudrun 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 remain
Gudrun A Rappold
Nature Reviews. Endocrinology
|
January 23, 2013
Height matters-from monogenic disorders to normal variation
Claudia Durand, Gudrun A Rappold
Molecular Psychiatry
|
May 29, 2020
Emerging evidence for gene mutations driving both brain and gut dysfunction in autism spectrum disorder
Beate Niesler, Gudrun A Rappold
Human Genetics
|
June 28, 2012
The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders
Claire Bacon, Gudrun A Rappold
Science in Context
|
September 1, 2022
Representing vulnerable populations in genetic studies: The case of the Roma
Veronika Lipphardt, Gudrun A Rappold, Mihai Surdu
Endocrine Reviews
|
June 30, 2016
A Track Record on SHOX: From Basic Research to Complex Models and Therapy
Antonio Marchini, Tsutomu Ogata, Gudrun A Rappold
Mechanisms of Development
|
November 7, 2012
The cellular function of srGAP3 and its role in neuronal morphogenesis
Claire Bacon, Volker Endris, Gudrun A Rappold
The Journal of Pediatrics
|
October 18, 2005
All shook up by SHOX deficiency
Gudrun A Rappold, Alan Shanske, Paul Saenger
Human Mutation
|
October 29, 2002
The human SHOX mutation database
Beate Niesler, Christine Fischer, Gudrun A Rappold
Page
of 8