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Publications by Bruce Smoller
A Novel Somatic Mutation of the 3β-Hydroxysteroid Dehydrogenase Gene in Sporadic Cutaneous Verruciform Xanthoma
Archives of Dermatology
Related publications
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
Rv1106c fromMycobacterium tuberculosisIs a 3β-Hydroxysteroid Dehydrogenase†
Biochemistry
Biochemistry
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
Vulvar Verruciform Xanthoma
Archives of Dermatology
The ADRENOGENITAL SYNDROME WITH DEFICIENCY OF 3β-Hydroxysteroid DEHYDROGENASE*
Journal of Clinical Investigation
Medicine
A Case of Verruciform Xanthoma in the Ventral Tongue.
Japanese Journal of Oral & Maxillofacial Surgery
Verruciform Xanthoma Behaving Badly
Pathology
Forensic Medicine
Pathology
Verruciform Xanthoma Located in Anterior Gingiva
Journal of Clinical and Experimental Dentistry
Dentistry
Conversion of Human Steroid 5β-Reductase (AKR1D1) Into 3β-Hydroxysteroid Dehydrogenase by Single Point Mutation E120H
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
