A missense mutation in the glucagon receptor gene is associated with non-insulin-dependent diabetes mellitus. Read more about A missense mutation in the glucagon receptor gene is associated with non-insulin-dependent diabetes mellitus.
Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population. Read more about Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population.
p53-deficient mice are extremely susceptible to radiation-induced tumorigenesis. Read more about p53-deficient mice are extremely susceptible to radiation-induced tumorigenesis.
Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease. Read more about Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease.
Polymorphism of a CAG trinucleotide repeat within Sry correlates with B6.YDom sex reversal. Read more about Polymorphism of a CAG trinucleotide repeat within Sry correlates with B6.YDom sex reversal.
Linkage mapping of dopa-responsive dystonia (DRD) to chromosome 14q. Read more about Linkage mapping of dopa-responsive dystonia (DRD) to chromosome 14q.
Nonsense mutations in the C-terminal SH2 region of the GTPase activating protein (GAP) gene in human tumours. Read more about Nonsense mutations in the C-terminal SH2 region of the GTPase activating protein (GAP) gene in human tumours.
Diminished support for linkage between manic depressive illness and X-chromosome markers in three Israeli pedigrees. Read more about Diminished support for linkage between manic depressive illness and X-chromosome markers in three Israeli pedigrees.
