Chromosomal localization of long trinucleotide repeats in the human genome by fluorescence in situ hybridization

Nature Genetics

Volumn 12, Issue 2, 1996, Pages 183-185

  Haaf, Thomas ^a   Sirugo, Giorgio ^b   Kidd, Kenneth K ^b   Ward, David C ^b  

^a MAX PLANCK INSTITUTE FOR MOLECULAR GENETICS   (Germany)

^b YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

TRINUCLEOTIDE;

ALLELE; ARTICLE; CHROMOSOME MAP; FLUORESCENCE IN SITU HYBRIDIZATION; FRAGILE X SYNDROME; GENETIC POLYMORPHISM; GOOD LABORATORY PRACTICE; HUMAN; HUNTINGTON CHOREA; MYOTONIC DYSTROPHY; PATHOGENESIS; PRIORITY JOURNAL; SCHIZOPHRENIA;

BASE SEQUENCE; BIOTIN; CHROMOSOME MAPPING; DNA PROBES; GENOME; HUMANS; IMAGE PROCESSING, COMPUTER-ASSISTED; IN SITU HYBRIDIZATION, FLUORESCENCE; MOLECULAR SEQUENCE DATA; SCHIZOPHRENIA, PARANOID; TRINUCLEOTIDE REPEATS;

EID: 0030034928     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0296-183     Document Type: Article

References (10)

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