Two new cases with microdeletion of 17q23.2 suggest presence of a candidate gene for sensorineural hearing loss within this region.

Schönewolf-Greulich, Bitten

Two new cases with microdeletion of 17q23.2 suggest presence of a candidate gene for sensorineural hearing loss within this region. [electronic resource] - American journal of medical genetics. Part A Dec 2011 - 2964-9 p. digital

Publication Type: Case Reports; Journal Article

1552-4833

10.1002/ajmg.a.34302 doi


Child
Child, Preschool
Chromosome Deletion
Chromosomes, Human, Pair 17
Comparative Genomic Hybridization
Female
Hearing Loss, Sensorineural--diagnosis
Humans
Infant
Polymorphism, Single Nucleotide
T-Box Domain Proteins--genetics