Genetic heterogeneity in benign familial neonatal convulsions: Identification of a new locus on chromosome 8q

American Journal of Human Genetics

Volumn 53, Issue 3, 1993, Pages 670-675

  Lewis, T B ^a   Leach, R J ^a   Ward, K ^a   O'Connell, P ^a   Ryan, S G ^a  

^a UNIVERSITY OF TEXAS HEALTH SCIENCE CENTER AT SAN ANTONIO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 20; CHROMOSOME 8Q; CHROMOSOME MAP; CONVULSION; FAMILIAL DISEASE; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENETIC MARKER; HUMAN; HUMAN CELL; NEWBORN DISEASE; PRIORITY JOURNAL; SEIZURE;

BASE SEQUENCE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 20; CHROMOSOMES, HUMAN, PAIR 8; EPILEPSY, GENERALIZED; HUMAN; INFANT; INFANT, NEWBORN; LINKAGE (GENETICS); LOD SCORE; MOLECULAR SEQUENCE DATA; PEDIGREE; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; REPETITIVE SEQUENCES, NUCLEIC ACID; SPASMS, INFANTILE; SUPPORT, U.S. GOV'T, P.H.S.; VARIATION (GENETICS);

EID: 0027359350     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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