Retinal abnormalities in three genetic disorders involving the X chromosome

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Podrobná bibliografia
Vydané v:	Journal francais d'ophtalmologie Ročník 43; číslo 10; s. 1107
Hlavní autori:	Falfoul, Y, El Leuch, I E, El Matri, K, Chaker, N, El Matri, L
Médium:	Journal Article
Jazyk:	French
Vydavateľské údaje:	France 01.12.2020
Predmet:	Aicardi Syndrome - diagnosis Aicardi Syndrome - genetics Child Chromosome Aberrations Chromosome Disorders - diagnosis Chromosome Disorders - genetics Chromosomes, Human, Pair 8 - genetics Chromosomes, Human, X - genetics Eye Abnormalities - diagnosis Eye Abnormalities - genetics Female Genetic Diseases, X-Linked - diagnosis Genetic Diseases, X-Linked - genetics Humans Infant Infant, Newborn Male Retina - abnormalities Retina - diagnostic imaging Retina - pathology Trisomy - diagnosis Trisomy - genetics Turner Syndrome - diagnosis Turner Syndrome - genetics
ISSN:	1773-0597, 1773-0597
On-line prístup:	Zistit podrobnosti o prístupe
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Popis
Bibliografia:	ObjectType-Case Study-2 SourceType-Scholarly Journals-1 ObjectType-Feature-4 content type line 23 ObjectType-Report-1 ObjectType-Article-3
ISSN:	1773-0597 1773-0597
DOI:	10.1016/j.jfo.2020.01.017