Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss

Articolo
Data di Pubblicazione:
2015
Tipologia CRIS:
01.01 Articolo in rivista
Keywords:
Choroideremia; Hypotonia; Interstitial deletions; Intellectual disability; X-linked hearing impairment
Elenco autori:
Autori di Ateneo:
Link alla scheda completa:
https://iris.cnr.it/handle/20.500.14243/294396
Pubblicato in:
MOLECULAR CYTOGENETICS
Journal