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C A Stratakis

Showing results (161-170 of 166) with videos related to

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Human Mutation|January 15, 1999
Mutation analyses of North American APS-1 patientsM Heino, H S Scott, Q Chen, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Report and abstracts of the Fourth International Workshop on Human Chromosome 2 Mapping 1996N K Spur, R Bashir, K Bushby, et al.
The Journal of Clinical Endocrinology and Metabolism|August 26, 1998
Carney complex, Peutz-Jeghers syndrome, Cowden disease, and Bannayan-Zonana syndrome share cutaneous and endocrine manifestations, but not genetic lociC A Stratakis, L S Kirschner, S E Taymans, et al.
Clinical Genetics|May 29, 2010
The role of germline AIP, MEN1, PRKAR1A, CDKN1B and CDKN2C mutations in causing pituitary adenomas in a large cohort of children, adolescents, and patients with genetic syndromesC A Stratakis, M A Tichomirowa, S Boikos, et al.
Journal of Medical Genetics|December 14, 2004
A transgenic mouse bearing an antisense construct of regulatory subunit type 1A of protein kinase A develops endocrine and other tumours: comparison with Carney complex and other PRKAR1A induced lesionsK J Griffin, L S Kirschner, L Matyakhina, et al.
Journal of Medical Genetics|May 4, 2004
Inhibin alpha-subunit (INHA) gene and locus changes in paediatric adrenocortical tumours from TP53 R337H mutation heterozygote carriersC A Longui, S H V Lemos-Marini, B Figueiredo, et al.
Pageof 17

Showing results (161-170 of 166) with videos related to

Sort By:
Pageof 17
You have reached the last page of results.This site can display upto 166 results.
Human Mutation|January 15, 1999
Mutation analyses of North American APS-1 patientsM Heino, H S Scott, Q Chen, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Report and abstracts of the Fourth International Workshop on Human Chromosome 2 Mapping 1996N K Spur, R Bashir, K Bushby, et al.
The Journal of Clinical Endocrinology and Metabolism|August 26, 1998
Carney complex, Peutz-Jeghers syndrome, Cowden disease, and Bannayan-Zonana syndrome share cutaneous and endocrine manifestations, but not genetic lociC A Stratakis, L S Kirschner, S E Taymans, et al.
Clinical Genetics|May 29, 2010
The role of germline AIP, MEN1, PRKAR1A, CDKN1B and CDKN2C mutations in causing pituitary adenomas in a large cohort of children, adolescents, and patients with genetic syndromesC A Stratakis, M A Tichomirowa, S Boikos, et al.
Journal of Medical Genetics|December 14, 2004
A transgenic mouse bearing an antisense construct of regulatory subunit type 1A of protein kinase A develops endocrine and other tumours: comparison with Carney complex and other PRKAR1A induced lesionsK J Griffin, L S Kirschner, L Matyakhina, et al.
Journal of Medical Genetics|May 4, 2004
Inhibin alpha-subunit (INHA) gene and locus changes in paediatric adrenocortical tumours from TP53 R337H mutation heterozygote carriersC A Longui, S H V Lemos-Marini, B Figueiredo, et al.
Pageof 17