Genomics Research Group

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Current research:

1.     Screening for human Heparan Sulfate proteoglycan gene mutations associated with Familial Schwartz Jampel Syndrome among Jordanian families.

2.     Screening for ATP1A2 gene mutations Associated with Familial Hemiplegic among Jordanian families.

3.     Screening for beta globin gene mutations Associated with β-thalassemia in Jordanian families.

4.     Screening for SERPING1 gene mutations Associated with Angioedema in Jordanian families.

5.     Screening for SPINK5 gene mutations Associated with Netherton Syndrome among Jordanian families.

6.     Screening for FBN1 gene mutations Associated with Marfan Syndrome among Jordanian families.

7.     Screening for MKS1 and MKS3 genes mutations Associated with Meckel Gruber Syndrome among Jordanian families.

8.     Screening for PKHD1 gene mutations Associated with polycystic kidney among Jordanian families.

9.     FV Leiden, MTHFR and F II mutation detection by molecular beacon real-time PCR assay. 

10.  Telomere length measurement and its relation to early ageing in Down syndrome patients.

 

 

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