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Colm Costigan

Showing results (11-20 of 17) with videos related to

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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 humansClaire 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 studyStephen 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 deficiencyLi 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 growthSally 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 IAntonella 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 developmentGwang-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 IAnne Puel, Rainer Döffinger, Angels Natividad, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 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 humansClaire 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 studyStephen 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 deficiencyLi 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 growthSally 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 IAntonella 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 developmentGwang-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 IAnne Puel, Rainer Döffinger, Angels Natividad, et al.
Pageof 2