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Rogier A Oldenburg

Showing results (21-30 of 43) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|December 17, 2015
Complex MAX Rearrangement in a Family With Malignant Pheochromocytoma, Renal Oncocytoma, and ErythrocytosisEsther Korpershoek, Djamailys Koffy, Bert H Eussen, et al.
The Journal of Clinical Endocrinology and Metabolism|November 28, 2017
Clinical Aspects of SDHA-Related Pheochromocytoma and Paraganglioma: A Nationwide StudyKarin van der Tuin, Arjen R Mensenkamp, Carli M J Tops, et al.
Investigative Ophthalmology & Visual Science|October 1, 2010
Expanding the spectrum of FOXC1 and PITX2 mutations and copy number changes in patients with anterior segment malformationsBarbara D'haene, Françoise Meire, Ilse Claerhout, et al.
Breast Cancer Research : BCR|November 11, 2010
A genome-wide association scan on estrogen receptor-negative breast cancerJingmei Li, Keith Humphreys, Hatef Darabi, et al.
Journal of the American College of Cardiology|May 29, 2012
Aggressive cardiovascular phenotype of aneurysms-osteoarthritis syndrome caused by pathogenic SMAD3 variantsDenise van der Linde, Ingrid M B H van de Laar, Aida M Bertoli-Avella, et al.
European Journal of Human Genetics : EJHG|July 11, 2018
Lack of evidence for a causal role of CALR3 in monogenic cardiomyopathyJudith M A Verhagen, Job H Veldman, Paul A van der Zwaag, et al.
Nature Genetics|January 11, 2011
Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritisIngrid M B H van de Laar, Rogier A Oldenburg, Gerard Pals, et al.
Circulation. Cardiovascular Genetics|August 10, 2017
<i>Lamin A/C</i>-Related Cardiac Disease: Late Onset With a Variable and Mild Phenotype in a Large Cohort of Patients With the Lamin A/C p.(Arg331Gln) Founder MutationEdgar T Hoorntje, Ilse A Bollen, Daniela Q Barge-Schaapveld, et al.
Journal of Medical Genetics|December 15, 2011
Phenotypic spectrum of the SMAD3-related aneurysms-osteoarthritis syndromeIngrid M B H van de Laar, Denise van der Linde, Edwin H G Oei, et al.
The Lancet. Oncology|July 7, 2009
An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysisFrancien H van Nederveen, José Gaal, Judith Favier, et al.
Pageof 5

Showing results (21-30 of 43) with videos related to

Sort By:
Pageof 5
The Journal of Clinical Endocrinology and Metabolism|December 17, 2015
Complex MAX Rearrangement in a Family With Malignant Pheochromocytoma, Renal Oncocytoma, and ErythrocytosisEsther Korpershoek, Djamailys Koffy, Bert H Eussen, et al.
The Journal of Clinical Endocrinology and Metabolism|November 28, 2017
Clinical Aspects of SDHA-Related Pheochromocytoma and Paraganglioma: A Nationwide StudyKarin van der Tuin, Arjen R Mensenkamp, Carli M J Tops, et al.
Investigative Ophthalmology & Visual Science|October 1, 2010
Expanding the spectrum of FOXC1 and PITX2 mutations and copy number changes in patients with anterior segment malformationsBarbara D'haene, Françoise Meire, Ilse Claerhout, et al.
Breast Cancer Research : BCR|November 11, 2010
A genome-wide association scan on estrogen receptor-negative breast cancerJingmei Li, Keith Humphreys, Hatef Darabi, et al.
Journal of the American College of Cardiology|May 29, 2012
Aggressive cardiovascular phenotype of aneurysms-osteoarthritis syndrome caused by pathogenic SMAD3 variantsDenise van der Linde, Ingrid M B H van de Laar, Aida M Bertoli-Avella, et al.
European Journal of Human Genetics : EJHG|July 11, 2018
Lack of evidence for a causal role of CALR3 in monogenic cardiomyopathyJudith M A Verhagen, Job H Veldman, Paul A van der Zwaag, et al.
Nature Genetics|January 11, 2011
Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritisIngrid M B H van de Laar, Rogier A Oldenburg, Gerard Pals, et al.
Circulation. Cardiovascular Genetics|August 10, 2017
<i>Lamin A/C</i>-Related Cardiac Disease: Late Onset With a Variable and Mild Phenotype in a Large Cohort of Patients With the Lamin A/C p.(Arg331Gln) Founder MutationEdgar T Hoorntje, Ilse A Bollen, Daniela Q Barge-Schaapveld, et al.
Journal of Medical Genetics|December 15, 2011
Phenotypic spectrum of the SMAD3-related aneurysms-osteoarthritis syndromeIngrid M B H van de Laar, Denise van der Linde, Edwin H G Oei, et al.
The Lancet. Oncology|July 7, 2009
An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysisFrancien H van Nederveen, José Gaal, Judith Favier, et al.
Pageof 5