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The Journal of Clinical Endocrinology and Metabolism
|
September 11, 2001
Genotype versus phenotype in families with androgen insensitivity syndrome
A L Boehmer, O Brinkmann, H Brüggenwirth, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 22, 1999
17Beta-hydroxysteroid dehydrogenase-3 deficiency: diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations
A L Boehmer, A O Brinkmann, L A Sandkuijl, 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 puberty
H Kremer, J W Martens, M van Reen, et al.
Page
of 14
Search research articles
Search
Showing results (131-140 of 133) with videos related to
Sort By:
Page
of 14
You have reached the last page of results.
This site can display upto 133 results.
The Journal of Clinical Endocrinology and Metabolism
|
September 11, 2001
Genotype versus phenotype in families with androgen insensitivity syndrome
A L Boehmer, O Brinkmann, H Brüggenwirth, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 22, 1999
17Beta-hydroxysteroid dehydrogenase-3 deficiency: diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations
A L Boehmer, A O Brinkmann, L A Sandkuijl, 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 puberty
H Kremer, J W Martens, M van Reen, et al.
Page
of 14