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La Revue De Medecine Interne
|
July 24, 2012
[Myelopathy due to Schistosoma mansoni]
F A Cisse, Y Morel, M A Bangoura, et al.
Archives Francaises De Pediatrie
|
August 1, 1985
[Value of the assay of urinary gonadotropins in pediatric endocrinology]
Y Morel, H La Selve, P Chatelain, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 1, 1995
Nonsalt-losing male pseudohermaphroditism due to the novel homozygous N100S mutation in the type II 3 beta-hydroxysteroid dehydrogenase gene
F Mébarki, R Sanchez, E Rhéaume, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
April 6, 2005
[Adrenal hypoplasia congenita: four new cases in children]
P Pélissier, E Merlin, F Prieur, et al.
Praxis
|
September 10, 1999
["I want to lose weight"]
A Golay, D Painot, Y Morel, et al.
Human Molecular Genetics
|
September 1, 1994
Functional characterization of the novel L108W and P186L mutations detected in the type II 3 beta-hydroxysteroid dehydrogenase gene of a male pseudohermaphrodite with congenital adrenal hyperplasia
R Sanchez, F Mébarki, E Rhéaume, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
December 1, 1995
Structure-function relationships and molecular genetics of the 3 beta-hydroxysteroid dehydrogenase gene family
J Simard, R Sanchez, F Durocher, et al.
Clinical Genetics
|
March 25, 2010
Only two mutations detected in 15 Tunisian patients with 11β-hydroxylase deficiency: the p.Q356X and the novel p.G379V
M Kharrat, S Trabelsi, M Chaabouni, et al.
The Journal of Clinical Investigation
|
February 1, 1989
Rearrangements and point mutations of P450c21 genes are distinguished by five restriction endonuclease haplotypes identified by a new probing strategy in 57 families with congenital adrenal hyperplasia
Y Morel, J André, B Uring-Lambert, et al.
The Journal of Endocrinology
|
September 1, 1996
Molecular biology and genetics of the 3 beta-hydroxysteroid dehydrogenase/delta5-delta4 isomerase gene family
J Simard, F Durocher, F Mébarki, et al.
Page
of 14
Search research articles
Search
Showing results (121-130 of 138) with videos related to
Sort By:
Page
of 14
La Revue De Medecine Interne
|
July 24, 2012
[Myelopathy due to Schistosoma mansoni]
F A Cisse, Y Morel, M A Bangoura, et al.
Archives Francaises De Pediatrie
|
August 1, 1985
[Value of the assay of urinary gonadotropins in pediatric endocrinology]
Y Morel, H La Selve, P Chatelain, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 1, 1995
Nonsalt-losing male pseudohermaphroditism due to the novel homozygous N100S mutation in the type II 3 beta-hydroxysteroid dehydrogenase gene
F Mébarki, R Sanchez, E Rhéaume, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
April 6, 2005
[Adrenal hypoplasia congenita: four new cases in children]
P Pélissier, E Merlin, F Prieur, et al.
Praxis
|
September 10, 1999
["I want to lose weight"]
A Golay, D Painot, Y Morel, et al.
Human Molecular Genetics
|
September 1, 1994
Functional characterization of the novel L108W and P186L mutations detected in the type II 3 beta-hydroxysteroid dehydrogenase gene of a male pseudohermaphrodite with congenital adrenal hyperplasia
R Sanchez, F Mébarki, E Rhéaume, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
December 1, 1995
Structure-function relationships and molecular genetics of the 3 beta-hydroxysteroid dehydrogenase gene family
J Simard, R Sanchez, F Durocher, et al.
Clinical Genetics
|
March 25, 2010
Only two mutations detected in 15 Tunisian patients with 11β-hydroxylase deficiency: the p.Q356X and the novel p.G379V
M Kharrat, S Trabelsi, M Chaabouni, et al.
The Journal of Clinical Investigation
|
February 1, 1989
Rearrangements and point mutations of P450c21 genes are distinguished by five restriction endonuclease haplotypes identified by a new probing strategy in 57 families with congenital adrenal hyperplasia
Y Morel, J André, B Uring-Lambert, et al.
The Journal of Endocrinology
|
September 1, 1996
Molecular biology and genetics of the 3 beta-hydroxysteroid dehydrogenase/delta5-delta4 isomerase gene family
J Simard, F Durocher, F Mébarki, et al.
Page
of 14