Fatimah Harun
Kuala Lumpur, Malaysia
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 8 publications
Malaysian Females With Congenital Adrenal Hyperplasia: Surgical Outcomes and Attitudes.
Journal: Frontiers in pediatrics
Published: September 10, 2018
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.
Journal: BMJ open
Published: January 08, 2015
Metabolic syndrome among 13 year old adolescents: prevalence and risk factors.
Journal: BMC public health
Published: December 02, 2014
Late onset X-linked adrenal hypoplasia congenita with hypogonadotropic hypgonadism due to a novel 4-bp deletion in exon 2 of NR0B1.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: April 10, 2014
Variable clinical phenotypes in a family with homozygous c.1159G>A mutation in the thyroid peroxidase gene.
Journal: Hormone research in paediatrics
Published: November 06, 2013
Functional analyses of C.2268dup in thyroid peroxidase gene associated with goitrous congenital hypothyroidism.
Journal: BioMed research international
Published: September 03, 2013
A Novel, Homozygous c.1502T>G (p.Val501Gly) Mutation in the Thyroid peroxidase Gene in Malaysian Sisters with Congenital Hypothyroidism and Multinodular Goiter.
Journal: International journal of endocrinology
Published: December 29, 2012
Permanent neonatal diabetes due to a novel insulin signal peptide mutation.
Journal: Pediatric diabetes
Published: May 29, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026