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Bell, Graeme
One or more keywords matched the following items that are connected to
Bell, Graeme
Item Type
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Concept
Chromosomes, Human, Pair 20
Academic Article
cDNA sequence and localization of polymorphic human cytosolic phosphoenolpyruvate carboxykinase gene (PCK1) to chromosome 20, band q13.31: PCK1 is not tightly linked to maturity-onset diabetes of the young.
Academic Article
Maturity onset diabetes of the young (MODY).
Academic Article
Dinucleotide repeat polymorphism in the NEC2 gene.
Academic Article
Structure and function of ASP, the human homolog of the mouse agouti gene.
Academic Article
A yeast artificial chromosome-based map of the region of chromosome 20 containing the diabetes-susceptibility gene, MODY1, and a myeloid leukemia related gene.
Academic Article
Abnormal insulin secretion, not insulin resistance, is the genetic or primary defect of MODY in the RW pedigree.
Academic Article
Altered insulin secretory responses to glucose in subjects with a mutation in the MODY1 gene on chromosome 20.
Academic Article
Dinucleotide repeat polymorphism at the human ribophorin II locus (RPN2) on chromosome 20q.
Academic Article
Molecular genetics of myeloid leukemia: identification of the commonly deleted segment of chromosome 20.
Academic Article
Human somatostatin receptor genes: localization of SSTR5 to human chromosome 20p11.2.
Search Criteria
Chromosomes Human Pair 20