Genetic heterogeneity of Usher syndrome.

Advances in oto-rhino-laryngology

Volumn 56, Issue , 2000, Pages 11-18

  Kimberling, W J ^a   Orten, D ^a   Pieke Dahl, S ^a  

^a BOYS TOWN NATIONAL RESEARCH HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MYOSIN;

CHROMOSOME 1; CHROMOSOME MAP; GENETICS; HEARING IMPAIRMENT; HUMAN; MENTAL DEFICIENCY; NEUROLOGIC DISEASE; RETINITIS PIGMENTOSA; REVIEW; SYNDROME; UNITED STATES;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; DEAFNESS; GAIT DISORDERS, NEUROLOGIC; HUMANS; MENTAL RETARDATION; MYOSINS; RETINITIS PIGMENTOSA; SYNDROME; UNITED STATES;

MLCS; MLOWN;

EID: 0033643157     PISSN: 00653071     EISSN: None     Source Type: Journal    
DOI: 10.1159/000059077     Document Type: Review

References (44)