Ontology highlight
ABSTRACT:
SUBMITTER: Leal SM
PROVIDER: S-EPMC6141006 | biostudies-literature | 1998 Jul-Aug
REPOSITORIES: biostudies-literature
Leal S M SM Apaydin F F Barnwell C C Iber M M Kandogan T T Pfister M M Braendle U U Cura O O Schwalb M M Zenner H P HP Vitale E E
European journal of human genetics : EJHG 19980701 4
A second kindred has been identified which supports the previously reported location of DFNB9. Linkage has been established to markers closely linked to DFNB9 which is located on 2p22-p23. The hearing impaired individuals in this highly consanguineous kindred from Eastern Turkey have prelingual profound hearing loss which affects all frequencies. A genetic map of the 2p22-p23 region where DFNB9 resides was generated using marker genotypes available from the CEPH database. All markers were placed ...[more]