عامل زواج الاقارب و دوره الرئیسی فی ارتفاع الامراض الوراثیة لنتزوج بوعی لیکن لدینا جیل سالم.

للاطباء : دراسات المختبر

فی هذا القسم قد بزل جهدا لتجمیع الدراسات المتخذه فی هذا المرکز و التی بثت بشکل مقالات و بوسترات و ملصقات لکی یستفید منها المحققی و الباحثی لهذا القسم.

Molecular detection of BRCA1 and BRCA 2 mutations in Iran

Beta-thalassemia minor due to HBB deletions with increased HbA2 and HbF

Results of molecular PGD in a private medical genetic lab report of 4 years results

Possible gonadal mosaism in two cases with unusual mutation pattern of PAH

Uniparental disomy of chromosome 12 which leads to a phenylketonuria case

Development and Validation of the “KBC-Aneuquick-V2 A QF-PCR assay for rapid prenatal diagnosis of aneuploidies

Coexistence of SMN1 deletion and duplication in unrelated cases

Frequency and heterozygosity of 10 STR markers linked to the HLA-gene-cluster for

Genetic screening and early cancer prevention in familiar cancers Authors

Molecular diagnosis of Factor VII gene in 5 Iranian families

NEW HUMAN IDENTIFICATION KIT WITH 30 MARKERS USING SHORT TANDEM REPEAT (STR) ANALYSIS

Variable Phenotypes Associated with Mutations in PAH Gene

 Detection of A New Mutation in TREX1 Gene Associated with Aicardi-Goutieres Syndrome

Rapid hla typing within family members, using 42 novel and highly informative microsatellites markers in multiplex pcr

Multiplex ligation-dependent probe amplification (MLPA): next step in the molecular diagnosis of thalassemias 

Validation of the Rizfiler PCR Amplification Kit-DNA Typing for Degraded Specimens

Identification of novel and reported mutations in usher related genes in two Iranian deaf families using targeted next-generation sequencing

Molecular analysis of ARSB gene in Iranian patients affected by Maroteaux–Lamy syndrome