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The top documents tagged [region of homozygosity]
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Mitochondrial complex III deficiency associated with a homozygous mutation in UQCRQ Ortal Barel Laboratory of Dr. Ohad Birk Ben Gurion University Beer-Sheva,
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Mutations in Lamin A are the Cause of Hutchinson-Gilford Progeria Syndrome Francis S. Collins, M.D., Ph.D. July 28, 2003
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Mitochondrial complex III deficiency associated with a homozygous mutation in UQCRQ Ortal Barel
47 views