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J S Parks

Showing results (161-170 of 164) with videos related to

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Science (New York, N.Y.)|August 21, 1992
Mutation of the POU-specific domain of Pit-1 and hypopituitarism without pituitary hypoplasiaR W Pfäffle, G E DiMattia, J S Parks, et al.
The Journal of Pediatrics|October 25, 2000
US newborn screening system guidelines II: follow-up of children, diagnosis, management, and evaluation. Statement of the Council of Regional Networks for Genetic Services (CORN)K A Pass, P A Lane, P M Fernhoff, et al.
Nature Genetics|February 14, 1998
Mutations in PROP1 cause familial combined pituitary hormone deficiencyW Wu, J D Cogan, R W Pfäffle, et al.
The Journal of Clinical Endocrinology and Metabolism|March 20, 1999
A limited repertoire of mutations of the luteinizing hormone (LH) receptor gene in familial and sporadic patients with male LH-independent precocious pubertyH Kremer, J W Martens, M van Reen, et al.
Pageof 17

Showing results (161-170 of 164) with videos related to

Sort By:
Pageof 17
You have reached the last page of results.This site can display upto 164 results.
Science (New York, N.Y.)|August 21, 1992
Mutation of the POU-specific domain of Pit-1 and hypopituitarism without pituitary hypoplasiaR W Pfäffle, G E DiMattia, J S Parks, et al.
The Journal of Pediatrics|October 25, 2000
US newborn screening system guidelines II: follow-up of children, diagnosis, management, and evaluation. Statement of the Council of Regional Networks for Genetic Services (CORN)K A Pass, P A Lane, P M Fernhoff, et al.
Nature Genetics|February 14, 1998
Mutations in PROP1 cause familial combined pituitary hormone deficiencyW Wu, J D Cogan, R W Pfäffle, et al.
The Journal of Clinical Endocrinology and Metabolism|March 20, 1999
A limited repertoire of mutations of the luteinizing hormone (LH) receptor gene in familial and sporadic patients with male LH-independent precocious pubertyH Kremer, J W Martens, M van Reen, et al.
Pageof 17