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The Journal of Clinical Investigation
|
February 23, 2012
MCM4 mutation causes adrenal failure, short stature, and natural killer cell deficiency in humans
Claire R Hughes, Leonardo Guasti, Eirini Meimaridou, et al.
Diabetes Care
|
March 13, 2009
Validation of continuous glucose monitoring in children and adolescents with cystic fibrosis: a prospective cohort study
Stephen M P O'Riordan, Peter Hindmarsh, Nathan R Hill, et al.
Clinical Endocrinology
|
January 28, 2009
Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiency
Li F Chan, Louise A Metherell, Heiko Krude, et al.
European Journal of Human Genetics : EJHG
|
January 27, 2011
The 12q14 microdeletion syndrome: six new cases confirming the role of HMGA2 in growth
Sally Ann Lynch, Nicola Foulds, Ann-Charlotte Thuresson, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 30, 2008
Autoantibodies against type I interferons as an additional diagnostic criterion for autoimmune polyendocrine syndrome type I
Antonella Meloni, Maria Furcas, Filomena Cetani, et al.
Journal of Medical Genetics
|
January 22, 2015
Copy number variation of two separate regulatory regions upstream of SOX9 causes isolated 46,XY or 46,XX disorder of sex development
Gwang-Jin Kim, Elisabeth Sock, Astrid Buchberger, et al.
The Journal of Experimental Medicine
|
February 4, 2010
Autoantibodies against IL-17A, IL-17F, and IL-22 in patients with chronic mucocutaneous candidiasis and autoimmune polyendocrine syndrome type I
Anne Puel, Rainer Döffinger, Angels Natividad, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 17) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 17 results.
The Journal of Clinical Investigation
|
February 23, 2012
MCM4 mutation causes adrenal failure, short stature, and natural killer cell deficiency in humans
Claire R Hughes, Leonardo Guasti, Eirini Meimaridou, et al.
Diabetes Care
|
March 13, 2009
Validation of continuous glucose monitoring in children and adolescents with cystic fibrosis: a prospective cohort study
Stephen M P O'Riordan, Peter Hindmarsh, Nathan R Hill, et al.
Clinical Endocrinology
|
January 28, 2009
Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiency
Li F Chan, Louise A Metherell, Heiko Krude, et al.
European Journal of Human Genetics : EJHG
|
January 27, 2011
The 12q14 microdeletion syndrome: six new cases confirming the role of HMGA2 in growth
Sally Ann Lynch, Nicola Foulds, Ann-Charlotte Thuresson, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 30, 2008
Autoantibodies against type I interferons as an additional diagnostic criterion for autoimmune polyendocrine syndrome type I
Antonella Meloni, Maria Furcas, Filomena Cetani, et al.
Journal of Medical Genetics
|
January 22, 2015
Copy number variation of two separate regulatory regions upstream of SOX9 causes isolated 46,XY or 46,XX disorder of sex development
Gwang-Jin Kim, Elisabeth Sock, Astrid Buchberger, et al.
The Journal of Experimental Medicine
|
February 4, 2010
Autoantibodies against IL-17A, IL-17F, and IL-22 in patients with chronic mucocutaneous candidiasis and autoimmune polyendocrine syndrome type I
Anne Puel, Rainer Döffinger, Angels Natividad, et al.
Page
of 2