Microphthalmia and chorioretinal lesions in a girl with an Xp22.2‐pter deletion and partial 3p trisomy: Clinical observations relevant to aicardi syndrome gene localization
Year: 1990
Type: article
Study design: Case Report
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2057382163
