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Pediatric Research
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May 1, 1992
Prevalence of human growth hormone-1 gene deletions among patients with isolated growth hormone deficiency from different populations
P E Mullis, A Akinci, C Kanaka, et al.
Pediatric Research
|
April 1, 1991
Constitutionally short stature: analysis of the insulin-like growth factor-I gene and the human growth hormone gene cluster
P E Mullis, M S Patel, P M Brickell, et al.
American Journal of Nephrology
|
January 1, 1994
Hypermagnesiuria in children with newly diagnosed insulin-dependent diabetes mellitus
M Roffi, C Kanaka, P E Mullis, et al.
Human Molecular Genetics
|
April 1, 1994
BamHI RFLP for the GHRHR locus
Y Cao, J K Wagner, A Eblé, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 24, 1999
Aromatase deficiency caused by a novel P450arom gene mutation: impact of absent estrogen production on serum gonadotropin concentration in a boy
J Deladoëy, C Flück, M Bex, et al.
European Journal of Pediatrics
|
June 1, 1994
Persistent microalbuminuria in adolescents with type I (insulin-dependent) diabetes mellitus is associated to early rather than late puberty. Results of a prospective longitudinal study
M Janner, S E Knill, P Diem, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 1, 1997
Aromatase deficiency in a female who is compound heterozygote for two new point mutations in the P450arom gene: impact of estrogens on hypergonadotropic hypogonadism, multicystic ovaries, and bone densitometry in childhood
P E Mullis, N Yoshimura, B Kuhlmann, et al.
Pediatric Research
|
December 1, 1995
Isolated growth hormone deficiency: testing the little mouse hypothesis in man and exclusion of mutations within the extracellular domain of the growth hormone-releasing hormone receptor
Y Cao, J K Wagner, P C Hindmarsh, et al.
Molecular and Cellular Endocrinology
|
April 9, 1999
Regulation of human growth hormone receptor gene transcription by triiodothyronine (T3)
P E Mullis, A Eblé, U Marti, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 1, 1992
Isolated growth hormone (GH) deficiency type IA associated with a 45-kilobase gene deletion within the human GH gene cluster
A Akinci, C Kanaka, A Eblé, et al.
Page
of 8
Search research articles
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Showing results (41-50 of 78) with videos related to
Sort By:
Page
of 8
Pediatric Research
|
May 1, 1992
Prevalence of human growth hormone-1 gene deletions among patients with isolated growth hormone deficiency from different populations
P E Mullis, A Akinci, C Kanaka, et al.
Pediatric Research
|
April 1, 1991
Constitutionally short stature: analysis of the insulin-like growth factor-I gene and the human growth hormone gene cluster
P E Mullis, M S Patel, P M Brickell, et al.
American Journal of Nephrology
|
January 1, 1994
Hypermagnesiuria in children with newly diagnosed insulin-dependent diabetes mellitus
M Roffi, C Kanaka, P E Mullis, et al.
Human Molecular Genetics
|
April 1, 1994
BamHI RFLP for the GHRHR locus
Y Cao, J K Wagner, A Eblé, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 24, 1999
Aromatase deficiency caused by a novel P450arom gene mutation: impact of absent estrogen production on serum gonadotropin concentration in a boy
J Deladoëy, C Flück, M Bex, et al.
European Journal of Pediatrics
|
June 1, 1994
Persistent microalbuminuria in adolescents with type I (insulin-dependent) diabetes mellitus is associated to early rather than late puberty. Results of a prospective longitudinal study
M Janner, S E Knill, P Diem, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 1, 1997
Aromatase deficiency in a female who is compound heterozygote for two new point mutations in the P450arom gene: impact of estrogens on hypergonadotropic hypogonadism, multicystic ovaries, and bone densitometry in childhood
P E Mullis, N Yoshimura, B Kuhlmann, et al.
Pediatric Research
|
December 1, 1995
Isolated growth hormone deficiency: testing the little mouse hypothesis in man and exclusion of mutations within the extracellular domain of the growth hormone-releasing hormone receptor
Y Cao, J K Wagner, P C Hindmarsh, et al.
Molecular and Cellular Endocrinology
|
April 9, 1999
Regulation of human growth hormone receptor gene transcription by triiodothyronine (T3)
P E Mullis, A Eblé, U Marti, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 1, 1992
Isolated growth hormone (GH) deficiency type IA associated with a 45-kilobase gene deletion within the human GH gene cluster
A Akinci, C Kanaka, A Eblé, et al.
Page
of 8