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D20S213, a microsatellite polymorphism near the D20S16 locus.
Evidence of gray matter reduction and dysfunction in chromosome 22q11.2 deletion syndrome.
Linkage of genetic markers on human chromosomes 20 and 12 to NIDDM in Caucasian sib pairs with a history of diabetic nephropathy.
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D20S213, a microsatellite polymorphism near the D20S16 locus.
Howard TD, Rothschild CB, Bowden DW. D20S213, a microsatellite polymorphism near the D20S16 locus. Hum Mol Genet. 1994 Apr; 3(4):677.
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PubMed
subject areas
Alleles
Base Sequence
Chromosomes, Human, Pair 20
Diabetes Mellitus
DNA Primers
DNA, Satellite
Genetic Markers
Humans
Molecular Sequence Data
Polymorphism, Genetic
authors with profiles
Timothy D. Howard PhD