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Publications by Roger G Sutcliffe
A Novel Homozygous Nonsense Mutation E135X in the Type II 3β-Hydroxysteroid Dehydrogenase Gene (3β-Hsd) of a Female Child With Salt-Losing Congenital Adrenal Hyperplasia (Cah). 32
Pediatric Research
Child Health
Pediatrics
Perinatology
Related publications
Clinical Perspectives in Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency
Endocrine
Mutation of 3β-Hydroxysteroid Dehydrogenase (3β-Hsd) at the 3′-Untranslated Region Is Associated With Adrenocortical Insufficiency
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
A Novel Somatic Mutation of the 3β-Hydroxysteroid Dehydrogenase Gene in Sporadic Cutaneous Verruciform Xanthoma
Archives of Dermatology
Rv1106c fromMycobacterium tuberculosisIs a 3β-Hydroxysteroid Dehydrogenase†
Biochemistry
Biochemistry
Serum Magnesium Level in the Salt-Losing Type of Congenital Adrenal Hyperplasia.
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Immunolocalization of Murine Type VI 3β-Hydroxysteroid Dehydrogenase in the Adrenal Gland, Testis, Skin, and Placenta
Molecular and Cellular Endocrinology
Biochemistry
Endocrinology
Molecular Biology
The ADRENOGENITAL SYNDROME WITH DEFICIENCY OF 3β-Hydroxysteroid DEHYDROGENASE*
Journal of Clinical Investigation
Medicine
A Test for Heterocygocity in Congenital Adrenal Hyperplasia (Cah)
Pediatric Research
Child Health
Pediatrics
Perinatology
Testicular Nodules in Congenital Adrenal Hyperplasia (Cah)
Pediatric Research
Child Health
Pediatrics
Perinatology
