A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3

Human Molecular Genetics

Volumn 4, Issue 10, 1995, Pages 1967-1972

  Lesperance, Marci M ^a   Hail, James W ^b,c   Bess, Fred H ^b,d   Fukushima, Kunihiro ^c   Jain, Pawan K ^a   Plopils, Barbara ^a   Agustin, Theresa B san ^a,e   Skarka, Hana ^a   Smith, Richard J H ^c   Wills, Marketa ^a   Wilcox, Edward R ^a  

^a NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS   (United States)

^b VANDERBILT UNIVERSITY   (United States)

^c UNIVERSITY OF IOWA   (United States)

^d VANDERBILT UNIVERSITY MEDICAL CENTER   (United States)

^e National Institute on Disability and Rehabilitation Research   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA MARKER; SATELLITE DNA;

ANIMAL MODEL; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 4P; CHROMOSOME 5; CLINICAL ARTICLE; COCHLEA; FEMALE; GENE MAPPING; GENETIC LINKAGE; GENETIC RECOMBINATION; HEARING IMPAIRMENT; HUMAN; HUMAN CELL; HUNTINGTON CHOREA; LOW FREQUENCY NOISE; MALE; MOUSE; NONHUMAN; PERCEPTION DEAFNESS; PRIORITY JOURNAL; VESTIBULAR LABYRINTH;

ADOLESCENT; ANIMAL; CASE REPORT; CHILD; CHILD, PRESCHOOL; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 4; COMPARATIVE STUDY; FEMALE; GENES, DOMINANT; GENETIC MARKERS; HEARING DISORDERS; HUMAN; HUNTINGTON DISEASE; LINKAGE (GENETICS); LOD SCORE; MALE; MICE; PEDIGREE; POLYMERASE CHAIN REACTION; RECOMBINATION, GENETIC;

EID: 0028892097     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/4.10.1967     Document Type: Article

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