Open AccessGenotype Phenotype Correlation and Variability in Microcephaly Associated With Chorioretinopathy or Familial Exudative Vitreoretinopathy
Author(s) -
М. Ф. Шурыгина,
Joseph M. Simonett,
Maria A. Parker,
Amanda Mitchell,
Florin Grigorian,
Jacob Lifton,
Aaron Nagiel,
А. А. Шпак,
Е. Л. Дадали,
Irina Mishina,
Richard G. Weleber,
Paul Yang,
Mark E. Pennesi
Publication year - 2020
Publication title -
investigative ophthalmology and visual science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.935
H-Index - 218
eISSN - 1552-5783
pISSN - 0146-0404
DOI - 10.1167/iovs.61.13.2
Subject(s) - microcephaly , medicine , ophthalmology , atrophy , phenotype , retinal , microphthalmia , pathology , genetics , biology , pediatrics , gene
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