Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13

Nature Genetics

Volumn 14, Issue 4, 1996, Pages 479-481

  Taylor, T D ^a   Litt, M ^a   Kramer, P ^a   Pandolfo, M ^a   Angelini, L ^a   Nardocci, N ^a   Davis, S ^a   Pineda, M ^a   Hattori, H ^a   Flett, P J ^a   Cilio, M R ^a   Bertini, E ^a   Hayflick, S J ^a  

^a OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 20P; FEMALE; GENE MAPPING; HALLERVORDEN SPATZ DISEASE; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 20; CONSANGUINITY; FEMALE; GENETIC MARKERS; HALLERVORDEN-SPATZ SYNDROME; HOMOZYGOTE; HUMANS; LINKAGE (GENETICS); MALE; PEDIGREE;

EID: 16144365391     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng1296-479     Document Type: Article

References (0)