Microcephaly with chorioretinopathy. A report of two dominant families and three sporadic cases.

van Genderen, M M; Schuil, J; Meire, F M

van Genderen, M M; Schuil, J; Meire, F M.

Affiliation

van Genderen MM; Bartiméus Institute for Visually Handicapped Children, Zeist, The Netherlands.

Ophthalmic Genet ; 18(4): 199-207, 1997 Dec.

Article in En | MEDLINE | ID: mdl-9457751

Subject(s)

Choroid Diseases/complications; Microcephaly/complications; Retinal Diseases/complications; Adult; Child; Child, Preschool; Choroid Diseases/genetics; Choroid Diseases/pathology; Female; Fluorescein Angiography; Fundus Oculi; Humans; Male; Microcephaly/genetics; Microcephaly/pathology; Pedigree; Retinal Diseases/genetics; Retinal Diseases/pathology

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Collection: 01-internacional Database: MEDLINE Main subject: Retinal Diseases / Choroid Diseases / Microcephaly Limits: Adult / Child / Child, preschool / Female / Humans / Male Language: En Journal: Ophthalmic Genet Journal subject: GENETICA MEDICA / OFTALMOLOGIA Year: 1997 Document type: Article Affiliation country: Netherlands Country of publication: United kingdom

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