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Publications by Samira Kalayinia
A Novel De Novo Dominant Mutation of NOTCH1 Gene in an Iranian Family With Non‐syndromic Congenital Heart Disease
Journal of Clinical Laboratory Analysis
Allergy
Immunology
Biochemistry
Public Health
Medical Laboratory Technology
Clinical Biochemistry
Hematology
Microbiology
Environmental
Occupational Health
Mosaic Trisomy 22 in a 4-Year-Old Boy With Congenital Heart Disease and General Hypotrophy: A Case Report
Journal of Clinical Laboratory Analysis
Allergy
Immunology
Biochemistry
Public Health
Medical Laboratory Technology
Clinical Biochemistry
Hematology
Microbiology
Environmental
Occupational Health
