TY  - GEN
AU  - Petek,Erwin
AU  - Windpassinger,Christian
AU  - Mach,Monika
AU  - Rauter,Ludwig
AU  - Scherer,Stephen W
AU  - Wagner,Klaus
AU  - Kroisel,Peter M
TI  - Molecular characterization of a 12q22-q24 deletion associated with congenital deafness: confirmation and refinement of the DFNA25 locus
SN  - 1552-4825
PY  - 2003///0807
KW  - Child
KW  - Chromosome Banding
KW  - Chromosome Deletion
KW  - Chromosome Mapping
KW  - methods
KW  - Chromosomes, Human, Pair 12
KW  - genetics
KW  - Family Health
KW  - Female
KW  - Genes, Dominant
KW  - Genotype
KW  - Hearing Loss
KW  - congenital
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Male
KW  - Microsatellite Repeats
KW  - Pedigree
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/ajmg.a.10155
ER  -