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C A Stratakis

Showing results (141-150 of 166) with videos related to

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Journal of Medical Genetics|August 3, 2004
A pleiomorphic GH pituitary adenoma from a Carney complex patient displays universal allelic loss at the protein kinase A regulatory subunit 1A (PRKARIA) locusI Bossis, A Voutetakis, L Matyakhina, et al.
Human Genetics|August 1, 1996
Sporadic cardiac myxomas and tumors from patients with Carney complex are not associated with activating mutations of the Gs alpha geneL DeMarco, C A Stratakis, W L Boson, et al.
Endocrine-Related Cancer|March 15, 2015
Integrity of the pheochromocytoma susceptibility TMEM127 gene in patients with pediatric malignanciesE E King, Y Qin, R A Toledo, et al.
American Journal of Medical Genetics|July 16, 1999
Small deletions in the type II collagen triple helix produce kniest dysplasiaD J Wilkin, A S Artz, S South, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1996
Nelson's syndrome associated with a somatic frame shift mutation in the glucocorticoid receptor geneM Karl, G Von Wichert, E Kempter, et al.
The Journal of Clinical Endocrinology and Metabolism|November 10, 2001
Spectrum of mutations of the AAAS gene in Allgrove syndrome: lack of mutations in six kindreds with isolated resistance to corticotropinF Sandrini, C Farmakidis, L S Kirschner, et al.
The Journal of Clinical Endocrinology and Metabolism|September 16, 2015
Lipoprotein Particles in Adolescents and Young Women With PCOS Provide Insights Into Their Cardiovascular RiskE Gourgari, M Lodish, R Shamburek, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 2, 2001
An inherited p53 mutation that contributes in a tissue-specific manner to pediatric adrenal cortical carcinomaR C Ribeiro, F Sandrini, B Figueiredo, et al.
Human Mutation|June 30, 2000
Genetic heterogeneity in Peutz-Jeghers syndromeL A Boardman, F J Couch, L J Burgart, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|January 23, 2016
GPR101 Mutations are not a Frequent Cause of Congenital Isolated Growth Hormone DeficiencyF Castinetti, A F Daly, C A Stratakis, et al.
Pageof 17

Showing results (141-150 of 166) with videos related to

Sort By:
Pageof 17
Journal of Medical Genetics|August 3, 2004
A pleiomorphic GH pituitary adenoma from a Carney complex patient displays universal allelic loss at the protein kinase A regulatory subunit 1A (PRKARIA) locusI Bossis, A Voutetakis, L Matyakhina, et al.
Human Genetics|August 1, 1996
Sporadic cardiac myxomas and tumors from patients with Carney complex are not associated with activating mutations of the Gs alpha geneL DeMarco, C A Stratakis, W L Boson, et al.
Endocrine-Related Cancer|March 15, 2015
Integrity of the pheochromocytoma susceptibility TMEM127 gene in patients with pediatric malignanciesE E King, Y Qin, R A Toledo, et al.
American Journal of Medical Genetics|July 16, 1999
Small deletions in the type II collagen triple helix produce kniest dysplasiaD J Wilkin, A S Artz, S South, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1996
Nelson's syndrome associated with a somatic frame shift mutation in the glucocorticoid receptor geneM Karl, G Von Wichert, E Kempter, et al.
The Journal of Clinical Endocrinology and Metabolism|November 10, 2001
Spectrum of mutations of the AAAS gene in Allgrove syndrome: lack of mutations in six kindreds with isolated resistance to corticotropinF Sandrini, C Farmakidis, L S Kirschner, et al.
The Journal of Clinical Endocrinology and Metabolism|September 16, 2015
Lipoprotein Particles in Adolescents and Young Women With PCOS Provide Insights Into Their Cardiovascular RiskE Gourgari, M Lodish, R Shamburek, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 2, 2001
An inherited p53 mutation that contributes in a tissue-specific manner to pediatric adrenal cortical carcinomaR C Ribeiro, F Sandrini, B Figueiredo, et al.
Human Mutation|June 30, 2000
Genetic heterogeneity in Peutz-Jeghers syndromeL A Boardman, F J Couch, L J Burgart, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|January 23, 2016
GPR101 Mutations are not a Frequent Cause of Congenital Isolated Growth Hormone DeficiencyF Castinetti, A F Daly, C A Stratakis, et al.
Pageof 17