Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

R M Couch

Showing results (11-20 of 20) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 20 results.
Experimental Cell Research|March 15, 1973
Androgen-stimulated labelling of chromosomal proteins by isolated prostate nucleiK M Anderson, M Slavik, A K Evans, et al.
Diabetes Care|March 1, 1997
High incidence of IDDM over 6 years in Edmonton, Alberta, CanadaE L Toth, K C Lee, R M Couch, et al.
The Journal of Pediatrics|June 1, 1984
Prolonged remission of Cushing disease after treatment with cyproheptadineR M Couch, P J Smail, H J Dean, et al.
American Journal of Medical Genetics|September 1, 1990
Syndrome of mental retardation, facial anomalies, hypopituitarism, and distal arthrogryposis in sibsD Chitayat, J G Hall, R M Couch, et al.
Clinical Endocrinology|February 1, 1991
Allgrove syndrome: an autosomal recessive syndrome of ACTH insensitivity, achalasia and alacrimaP S Moore, R M Couch, Y S Perry, et al.
American Journal of Human Genetics|December 1, 1986
An autosomal dominant form of adolescent multinodular goiterR M Couch, I A Hughes, D J DeSa, et al.
American Journal of Medical Genetics|September 15, 1991
Hepatic dysfunction in Alström diseaseM B Connolly, J E Jan, R M Couch, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1989
Combined 17-hydroxylase and 17,20-desmolase deficiencies: evidence for synthesis of a defective cytochrome P450c17J S Winter, R M Couch, J Muller, et al.
American Journal of Medical Genetics|August 1, 1990
Apparent postnatal onset of some manifestations of the Wiedemann-Beckwith syndromeD Chitayat, A Rothchild, E Ling, et al.
Thyroid : Official Journal of the American Thyroid Association|February 12, 1998
A novel point mutation of thyroid hormone receptor beta gene in a family with resistance to thyroid hormoneT Nagashima, H Yagi, K Nagashima, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Experimental Cell Research|March 15, 1973
Androgen-stimulated labelling of chromosomal proteins by isolated prostate nucleiK M Anderson, M Slavik, A K Evans, et al.
Diabetes Care|March 1, 1997
High incidence of IDDM over 6 years in Edmonton, Alberta, CanadaE L Toth, K C Lee, R M Couch, et al.
The Journal of Pediatrics|June 1, 1984
Prolonged remission of Cushing disease after treatment with cyproheptadineR M Couch, P J Smail, H J Dean, et al.
American Journal of Medical Genetics|September 1, 1990
Syndrome of mental retardation, facial anomalies, hypopituitarism, and distal arthrogryposis in sibsD Chitayat, J G Hall, R M Couch, et al.
Clinical Endocrinology|February 1, 1991
Allgrove syndrome: an autosomal recessive syndrome of ACTH insensitivity, achalasia and alacrimaP S Moore, R M Couch, Y S Perry, et al.
American Journal of Human Genetics|December 1, 1986
An autosomal dominant form of adolescent multinodular goiterR M Couch, I A Hughes, D J DeSa, et al.
American Journal of Medical Genetics|September 15, 1991
Hepatic dysfunction in Alström diseaseM B Connolly, J E Jan, R M Couch, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1989
Combined 17-hydroxylase and 17,20-desmolase deficiencies: evidence for synthesis of a defective cytochrome P450c17J S Winter, R M Couch, J Muller, et al.
American Journal of Medical Genetics|August 1, 1990
Apparent postnatal onset of some manifestations of the Wiedemann-Beckwith syndromeD Chitayat, A Rothchild, E Ling, et al.
Thyroid : Official Journal of the American Thyroid Association|February 12, 1998
A novel point mutation of thyroid hormone receptor beta gene in a family with resistance to thyroid hormoneT Nagashima, H Yagi, K Nagashima, et al.
Pageof 2