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Volumn 89, Issue 3, 1999, Pages 121-122
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Hereditary deafness
a
a
NONE
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Author keywords
[No Author keywords available]
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Indexed keywords
CONNEXIN 26;
MYOSIN;
COCHLEA PROSTHESIS;
EDITORIAL;
GENE FREQUENCY;
GENE MUTATION;
GENETIC COUNSELING;
GENETIC DISORDER;
GENETIC HETEROGENEITY;
HAIR CELL;
HEARING;
HEARING IMPAIRMENT;
INNER EAR;
INTERPERSONAL COMMUNICATION;
POTASSIUM METABOLISM;
PRIORITY JOURNAL;
SIGN LANGUAGE;
USHER SYNDROME;
VERBAL COMMUNICATION;
DEAFNESS;
GENETIC DISEASES, INBORN;
HUMAN;
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EID: 0033600950
PISSN: 01487299
EISSN: None
Source Type: Journal
DOI: 10.1002/(SICI)1096-8628(19990924)89:3<121::AID-AJMG1>3.0.CO;2-U Document Type: Editorial |
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Times cited : (8)
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References (2)
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