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Pritchard et al., 1992 - Google Patents

Recombination of 4p16 DNA markers in an unusual family with Huntington disease

Pritchard et al., 1992

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Document ID
11936064341063944573
Author
Pritchard C
Zhu N
Zuo J
Bull L
Pericak-Vance M
Vance J
Roses A
Milatovich A
Francke U
Cox D
Myers R
Publication year
Publication venue
American journal of human genetics

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Snippet

The Huntington disease (HD) mutation has been localized to human chromosome 4p16, in a 6-Mb region between the D4S10 locus and the 4p telomere. In a report by Robbins et al., a family was identified in which an affected individual failed to inherit three alleles within the 6 …
Continue reading at pmc.ncbi.nlm.nih.gov (PDF) (other versions)

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    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions
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