TY  - GEN
AU  - Schönewolf-Greulich,Bitten
AU  - Ronan,Anne
AU  - Ravn,Kristine
AU  - Baekgaard,Peter
AU  - Lodahl,Marianne
AU  - Nielsen,Kate
AU  - Rendtorff,Nanna D
AU  - Tranebjaerg,Lisbeth
AU  - Brøndum-Nielsen,Karen
AU  - Tümer,Zeynep
TI  - Two new cases with microdeletion of 17q23.2 suggest presence of a candidate gene for sensorineural hearing loss within this region
SN  - 1552-4833
PY  - 2012///0430
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 17
KW  - Comparative Genomic Hybridization
KW  - Female
KW  - Hearing Loss, Sensorineural
KW  - diagnosis
KW  - Humans
KW  - Infant
KW  - Polymorphism, Single Nucleotide
KW  - T-Box Domain Proteins
KW  - genetics
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1002/ajmg.a.34302
ER  -