Ads
-
Related paper
- Familial adenomatous polyposis associated APC gene mutation - A case study
- Familial Adenomatous Polyposis: Gardner Syndrome. Case Report
- Endoscopic Mucosal Resection for Treatment of Multiple Early Gastric Cancer Complicating Familial Adenomatous Polyposis: A Case Report
- The Familial Adenomatous Polyposis. A Difficult Problem, Between Prevention and Treatment
- PROGRESSIVE FAMILIAL HEART BLOCK ASSOCIATED WITH A MUTATION IN GENE TRPM4: A MOROCCAN FAMILY CASE
- A Compound Heterozygous HBB: C.79G>A Associated with HBB: C.-78A>G Mutation of HBB Gene Leading to Β-Thalassemia Intermedia in A Vietnamese Patient: A Case Study |Biomedgrid
- A familial case of Marfan syndrome: a novel variant in the FBN1 gene
- Identification of compound heterozygosity for a rare beta-globin gene mutation, codon 15 (-T) with a common mutation IVS1-5 (G>C) by direct sequencing in a Bangladeshi patient
- A New Gene Mutation of PRKAR1A was found in a Carney Complex Case
- Ovarian Cancer and Mutation 5382insC in BRCA1 Gene (Clinical Case)
