A 405-kb cosmid contig and HindIII restriction map of the progressive myoclonus epilepsy type 1 (EPM1) candidate region in 21q22.3

Genomics

Volumn 29, Issue 1, 1995, Pages 288-290

  Lafrenière, Ronald G ^a   de Jong, Pieter J ^b   Rouleau, Guy A ^a  

^a MONTREAL GENERAL HOSPITAL   (Canada)

^b ROSWELL PARK CANCER INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 21Q; COSMID; GENE MAPPING; GENETIC DISORDER; HUMAN; MYOCLONUS EPILEPSY; PRIORITY JOURNAL;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 21; COSMIDS; DEOXYRIBONUCLEASE HINDIII; EPILEPSIES, MYOCLONIC; GENE LIBRARY; GENETIC MARKERS; HUMAN; LINKAGE (GENETICS); RESTRICTION MAPPING; SUPPORT, NON-U.S. GOV'T;

EID: 0029118590     PISSN: 08887543     EISSN: 10898646     Source Type: Journal    
DOI: 10.1006/geno.1995.1248     Document Type: Article

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