Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3

American Journal of Human Genetics

Volumn 58, Issue 6, 1996, Pages 1254-1259

  Bonne Tamir, B ^a   DeStefano, A L ^a   Briggs, C E ^a   Adair, R ^a   Franklyn, B ^a   Weiss, S ^a   Korostishevsky, M ^a   Frydman, M ^a   Baldwin, C T ^a   Farrer, L A ^a  

^a BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHILD; CHROMOSOME 21Q; CONGENITAL DEAFNESS; FEMALE; GENE LOCUS; GENETIC DISTANCE; GENETIC LINKAGE; HOMOZYGOSITY; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; TELOMERE;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 21; DEAFNESS; FEMALE; GENES, RECESSIVE; GENETIC MARKERS; HAPLOTYPES; HETEROZYGOTE DETECTION; HUMANS; INCIDENCE; INFANT, NEWBORN; ISRAEL; LINKAGE (GENETICS); LOD SCORE; MALE; PEDIGREE; TELOMERE;

EID: 0029883986     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)