Comparison of three methods to estimate genetic ancestry and control for stratification in genetic association studies among admixed populations. Read more about Comparison of three methods to estimate genetic ancestry and control for stratification in genetic association studies among admixed populations.
Gene symbol: KCNQ2. Disease: Benign neonatal familial convulsion. Read more about Gene symbol: KCNQ2. Disease: Benign neonatal familial convulsion.
Argininosuccinate lyase (ASL) deficiency: mutation analysis in 27 patients and a completed structure of the human ASL gene. Read more about Argininosuccinate lyase (ASL) deficiency: mutation analysis in 27 patients and a completed structure of the human ASL gene.
A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects. Read more about A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects.
Prevalence of BRCA1 and BRCA2 mutations among clinic-based African American families with breast cancer. Read more about Prevalence of BRCA1 and BRCA2 mutations among clinic-based African American families with breast cancer.
Fine-resolution mapping by haplotype evaluation: the examples of PFIC1 and BRIC. Read more about Fine-resolution mapping by haplotype evaluation: the examples of PFIC1 and BRIC.
Benign recurrent intrahepatic cholestasis (BRIC): evidence of genetic heterogeneity and delimitation of the BRIC locus to a 7-cM interval between D18S69 and D18S64. Read more about Benign recurrent intrahepatic cholestasis (BRIC): evidence of genetic heterogeneity and delimitation of the BRIC locus to a 7-cM interval between D18S69 and D18S64.
Carrier and prenatal diagnosis of X-linked severe combined immunodeficiency: mutation detection methods and utilization. Read more about Carrier and prenatal diagnosis of X-linked severe combined immunodeficiency: mutation detection methods and utilization.
Genetic analysis of the catalytic domain of the GAP gene in human lung cancer cell lines. Read more about Genetic analysis of the catalytic domain of the GAP gene in human lung cancer cell lines.
The human placental protein 14 (PP14) gene is localized on chromosome 9q34. Read more about The human placental protein 14 (PP14) gene is localized on chromosome 9q34.
