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Phenotypic evidence for a common pathogenesis in X-linked deafness pedigrees and in Xq13-q21 deletion related deafness

✍ Scribed by Reardon, W. ;Roberts, S. ;Phelps, P. D. ;Thomas, N. S. ;Beck, L. ;Issac, R. ;Hughes, H. E.


Book ID
102702098
Publisher
John Wiley and Sons
Year
1992
Tongue
English
Weight
506 KB
Volume
44
Category
Article
ISSN
0148-7299

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