W M But

Molecular analysis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Hong Kong Chinese patients

Angel OK Chan, W M But, KL Ng et al. · Steroids · 2011 · 39 citations

Adrenal Gland, Urology, Congenital Adrenal Hyperplasia +7

Glucose‐6‐phosphatase gene (727G→T) splicing mutation is prevalent in Hong Kong Chinese patients with glycogen storage disease type la

Ching‐Wan Lam, W M But, Chi‐Chung Shek et al. · Clinical Genetics · 1998 · 36 citations

Delayed diagnosis of adrenal insufficiency in a patient with severe penoscrotal hypospadias due to two novel P450 side-change cleavage enzyme (CYP11A1) mutations (p.R360W; p.R405X)

Silvia Parajes, A. O. Chan, W M But et al. · European Journal of Endocrinology · 2012 · 28 citations · Full text

Ambiguous genitalia, impaired steroidogenesis, and Antley-Bixler syndrome in a patient with P450 oxidoreductase deficiency.

W M But, Ivan F. M. Lo, CC Shek et al. · PubMed · 2010 · 20 citations

Infertility, Urology, Andrology +13

A novel nonsense mutation in the LPL gene in a Chinese neonate with hypertriglyceridemia

Angel On-Kei Chan, W M But, Wing-yee Tse et al. · Clinica Chimica Acta · 2006 · 16 citations

Metabolic Syndrome, Metabolic Disorder, Genetic Disorder +9