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Nature Genetics
|
May 1, 1997
A dominant-negative mutation of the growth hormone receptor causes familial short stature
R M Ayling, R Ross, P Towner, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
April 2, 1999
New growth hormone receptor exon 9 mutation causes genetic short stature
R M Ayling, R J Ross, P Towner, et al.
The EMBO Journal
|
March 15, 1994
A single amino acid substitution in the exoplasmic domain of the human growth hormone (GH) receptor confers familial GH resistance (Laron syndrome) with positive GH-binding activity by abolishing receptor homodimerization
P Duquesnoy, M L Sobrier, B Duriez, et al.
Psychological Medicine
|
June 13, 2023
White matter, cognition and psychotic-like experiences in UK Biobank
M J Bosma, S R Cox, T Ziermans, et al.
Clinical Endocrinology
|
March 1, 2012
Temozolomide in the management of dopamine agonist-resistant prolactinomas
B C Whitelaw, D Dworakowska, N W Thomas, et al.
Journal of Inherited Metabolic Disease
|
August 16, 2008
Recurrent acute liver failure and mitochondriopathy in a case of Wolcott-Rallison syndrome
G Engelmann, J Meyburg, N Shahbek, et al.
Translational Psychiatry
|
April 29, 2020
Psychotic-like experiences, polygenic risk scores for schizophrenia, and structural properties of the salience, default mode, and central-executive networks in healthy participants from UK Biobank
C Alloza, M Blesa-Cábez, M E Bastin, et al.
Molecular Psychiatry
|
January 5, 2021
Three major dimensions of human brain cortical ageing in relation to cognitive decline across the eighth decade of life
S R Cox, M A Harris, S J Ritchie, et al.
Page
of 4
Search research articles
Search
Showing results (31-40 of 38) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 38 results.
Nature Genetics
|
May 1, 1997
A dominant-negative mutation of the growth hormone receptor causes familial short stature
R M Ayling, R Ross, P Towner, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
April 2, 1999
New growth hormone receptor exon 9 mutation causes genetic short stature
R M Ayling, R J Ross, P Towner, et al.
The EMBO Journal
|
March 15, 1994
A single amino acid substitution in the exoplasmic domain of the human growth hormone (GH) receptor confers familial GH resistance (Laron syndrome) with positive GH-binding activity by abolishing receptor homodimerization
P Duquesnoy, M L Sobrier, B Duriez, et al.
Psychological Medicine
|
June 13, 2023
White matter, cognition and psychotic-like experiences in UK Biobank
M J Bosma, S R Cox, T Ziermans, et al.
Clinical Endocrinology
|
March 1, 2012
Temozolomide in the management of dopamine agonist-resistant prolactinomas
B C Whitelaw, D Dworakowska, N W Thomas, et al.
Journal of Inherited Metabolic Disease
|
August 16, 2008
Recurrent acute liver failure and mitochondriopathy in a case of Wolcott-Rallison syndrome
G Engelmann, J Meyburg, N Shahbek, et al.
Translational Psychiatry
|
April 29, 2020
Psychotic-like experiences, polygenic risk scores for schizophrenia, and structural properties of the salience, default mode, and central-executive networks in healthy participants from UK Biobank
C Alloza, M Blesa-Cábez, M E Bastin, et al.
Molecular Psychiatry
|
January 5, 2021
Three major dimensions of human brain cortical ageing in relation to cognitive decline across the eighth decade of life
S R Cox, M A Harris, S J Ritchie, et al.
Page
of 4