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Human Genetics
|
June 29, 2007
Gene symbol: CYP21A2
Veronique T V Tardy
Human Genetics
|
June 29, 2007
Gene symbol: CYP21A2
Veronique T V Tardy
Human Genetics
|
June 29, 2007
Gene symbol: CYP21A2
Veronique T V Tardy
Human Genetics
|
June 29, 2007
Gene symbol: CYP21A2
Veronique T V Tardy, Yves Morel
Human Genetics
|
June 29, 2007
Gene symbol: CYP21A2
Veronique T V Tardy, Yves Morel
Human Genetics
|
June 29, 2007
Gene symbol: CYP21A2
Veronique T V Tardy, Yves Morel
Annales D'Endocrinologie
|
July 1, 2005
21-Hydroxylase deficiency: an exemplary model of the contribution of molecular biology in the understanding and management of the disease
M G Forest, V Tardy, M Nicolino, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 3, 2001
How a patient homozygous for a 30-kb deletion of the C4-CYP 21 genomic region can have a nonclassic form of 21-hydroxylase deficiency
D L'Allemand, V Tardy, A Grüters, et al.
Annales D'Endocrinologie
|
April 7, 2004
[21 hydroxylase deficiency: new strategies emerging from molecular studies]
Y Morel, V Tardy, J-M Costa, et al.
Annales D'Endocrinologie
|
January 15, 2010
Detection and management of late-onset 21-hydroxylase deficiency in women with hyperandrogenism
J Young, V Tardy, A-B de la Perrière, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 22) with videos related to
Sort By:
Page
of 3
Human Genetics
|
June 29, 2007
Gene symbol: CYP21A2
Veronique T V Tardy
Human Genetics
|
June 29, 2007
Gene symbol: CYP21A2
Veronique T V Tardy
Human Genetics
|
June 29, 2007
Gene symbol: CYP21A2
Veronique T V Tardy
Human Genetics
|
June 29, 2007
Gene symbol: CYP21A2
Veronique T V Tardy, Yves Morel
Human Genetics
|
June 29, 2007
Gene symbol: CYP21A2
Veronique T V Tardy, Yves Morel
Human Genetics
|
June 29, 2007
Gene symbol: CYP21A2
Veronique T V Tardy, Yves Morel
Annales D'Endocrinologie
|
July 1, 2005
21-Hydroxylase deficiency: an exemplary model of the contribution of molecular biology in the understanding and management of the disease
M G Forest, V Tardy, M Nicolino, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 3, 2001
How a patient homozygous for a 30-kb deletion of the C4-CYP 21 genomic region can have a nonclassic form of 21-hydroxylase deficiency
D L'Allemand, V Tardy, A Grüters, et al.
Annales D'Endocrinologie
|
April 7, 2004
[21 hydroxylase deficiency: new strategies emerging from molecular studies]
Y Morel, V Tardy, J-M Costa, et al.
Annales D'Endocrinologie
|
January 15, 2010
Detection and management of late-onset 21-hydroxylase deficiency in women with hyperandrogenism
J Young, V Tardy, A-B de la Perrière, et al.
Page
of 3