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Publications by Siti Hida Hajira Mohamad Arif
A Novel Single Gene Deletion (-αMAL3.5) Giving Rise to Silent Α Thalassemia Carrier Removing the Entire HBA2 Gene Observed in Two Chinese Patients With Hb H Disease: Case Report of Two Probands
Thalassemia Reports
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610 Α-Thalassemia SILENT CARRIER WITH HEMOGLOBINS S AND C
Pediatric Research
Child Health
Pediatrics
Perinatology
A Prospective Analysis for Prevalence of Complications in Thai Non-Transfusion-Dependent Hb E/Β-Thalassemia and Α-Thalassemia (Hb H Disease)
American Journal of Hematology
Hematology
Identification and Characterization of a Novel 43-Bp Deletion Mutation of the ATP7B Gene in a Chinese Patient With Wilson’s Disease: A Case Report
BMC Medical Genetics
Genetics
Case Report: Maple Syrup Urine Disease With a Novel DBT Gene Mutation
BMC Pediatrics
Child Health
Pediatrics
Perinatology
Deletion of Entire LMNA Gene as a Cause of Cardiomyopathy
HeartRhythm Case Reports
Cardiovascular Medicine
Cardiology
Two Novel Molecular Defects in the LCAT Gene Are Associated With Fish Eye Disease
Arteriosclerosis, Thrombosis, and Vascular Biology
Cardiovascular Medicine
Cardiology
First Report of a Deletion Encompassing an Entire Exon in the Homogentisate 1,2-Dioxygenase Gene Causing Alkaptonuria
PLoS ONE
Multidisciplinary
Two Different Molecular Organizations Account for the Single Alpha-Globin Gene of the Alpha-Thalassemia-2 Genotype.
Journal of Clinical Investigation
Medicine
Case Report: Two Novel VPS13B Mutations in a Chinese Family With Cohen Syndrome and Hyperlinear Palms
BMC Medical Genetics
Genetics
