B H Rich - JoVE Visualize

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Filters

B H Rich

Showing results (11-20 of 14) with videos related to

Pageof 2

Sort By:

You have reached the last page of results.This site can display upto 14 results.

The Journal of Clinical Endocrinology and Metabolism|August 1, 1980

Pubertal presentation of congenital delta 5-3 beta-hydroxysteroid dehydrogenase deficiencyR L Rosenfield, B H Rich, J I Wolfsdorf, et al.

Hormone Research|March 4, 1998

Central hypothyroidism reveals compound heterozygous mutations in the Pit-1 geneM R Brown, J S Parks, M E Adess, et al.

The New England Journal of Medicine|May 8, 1998

Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase geneC A Stanley, Y K Lieu, B Y Hsu, et al.

The Journal of Pediatrics|July 1, 1979

Familial nesidioblastosis: severe neonatal hypoglycemia in two familiesS S Schwartz, B H Rich, A W Lucky, et al.

Pageof 2

Search research articles

Showing results (11-20 of 14) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 14 results.

The Journal of Clinical Endocrinology and Metabolism|August 1, 1980

Pubertal presentation of congenital delta 5-3 beta-hydroxysteroid dehydrogenase deficiencyR L Rosenfield, B H Rich, J I Wolfsdorf, et al.

Hormone Research|March 4, 1998

Central hypothyroidism reveals compound heterozygous mutations in the Pit-1 geneM R Brown, J S Parks, M E Adess, et al.

The New England Journal of Medicine|May 8, 1998

Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase geneC A Stanley, Y K Lieu, B Y Hsu, et al.

The Journal of Pediatrics|July 1, 1979

Familial nesidioblastosis: severe neonatal hypoglycemia in two familiesS S Schwartz, B H Rich, A W Lucky, et al.

Pageof 2