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Okihiro syndrome and acro-renal-ocular syndrome: clinical overlap, expansion of the phenotype, and absence of PAX2 mutations in two new families

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Bibliographic Details
Published in:	Journal of medical genetics 2002-01, Vol.39 (1), p.68-71
Main Authors:	Becker, K, Beales, PL, Calver, D M, Matthijs, G, Mohammed, S N
Format:	Article
Language:	English
Subjects:	Abnormalities, Multiple - genetics acro-renal-ocular syndrome Adult DNA-Binding Proteins - genetics Duane Retraction Syndrome - genetics Eye Abnormalities - genetics Eye diseases Families & family life Female Fingers & toes Genetic aspects Genetic disorders Hand Deformities, Congenital - genetics Hearing loss Hearing Loss, Sensorineural - genetics Humans Infant, Newborn Kidney - abnormalities Kidney diseases Letter to JMG Male Mutation Mutation - genetics Okihiro syndrome Optic nerve Parents & parenting Patients PAX2 Transcription Factor Phenotype Syndrome Transcription Factors - genetics Ultrasonic imaging Urogenital system
Citations:	Items that cite this one
Online Access:	Get full text
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