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Dinucleotide repeat polymorphisms at the P1, HBE1 and MYH7 loci.
[Autosomal-dominant osteopetrosis in Chuvashiya].
[Angiotensin-converting enzyme gene as a possible risk factor or protective factor in Alzheimer's disease].
Human hair growth deficiency is linked to a genetic defect in the phospholipase gene LIPH.
Genotype analysis identifies the cause of the "royal disease".
[Gene insertion and deletion polymorphism in the serotonin transporter gene and personality traits measured by MMPI].
Whole-genome sequencing identifies a novel ABCB7 gene mutation for X-linked congenital cerebellar ataxia in a large family of Mongolian ancestry.