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You searched for: Author/Creator Harun, Fatimah

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1. A multicenter study of endocrine abnormalities in septo-optic dysplasia (SOD) in Asean countries. (December 2015)

2. A Novel, Homozygous c.1502T>G (p.Val501Gly) Mutation in the Thyroid peroxidase Gene in Malaysian Sisters with Congenital Hypothyroidism and Multinodular Goiter. (28th April 2013)

3. Congenital Hypothyroidism: An Audit and Study of Different Cord Blood Screening TSH Values in a Tertiary Medical Centre in Malaysia. (27th October 2015)

7. Prevalence of c.2268dup and detection of two novel alterations, c.670_672del and c.1186C>T, in the TPO gene in a cohort of Malaysian–Chinese with thyroid dyshormonogenesis. Issue 1 (5th January 2015)