A new association of congenital hydrocephalus, albinism, megalocornea, and retinal coloboma in a syndromic child: A clinical and genetic study

Ophthalmic Genetics

Volumn 21, Issue 4, 2000, Pages 211-216

  Dube P ^a   Der Kaloustian, V M ^a   Demczuk, S ^a   Saabti, H ^a   Koenekoop, R K ^a  

^a MONTREAL CHILDREN S HOSPITAL   (Canada)

Author keywords

Albinism; Cryptorchidism; Hydrocephalus; Megalocornea; Monosomy 9p; Retinal coloboma

Indexed keywords

ALBINISM; ARTICLE; CASE REPORT; CHROMOSOME 9P; CHROMOSOME DELETION; CLINICAL FEATURE; COLOBOMA; CONGENITAL HYDROCEPHALUS; CORNEA DISEASE; CRYPTORCHISM; DEVELOPMENTAL DISORDER; DISEASE ASSOCIATION; GENETIC ANALYSIS; HUMAN; INFANT; MALE; MOLECULAR GENETICS; PRIORITY JOURNAL; RETINA DISEASE; SYNDROME;

EID: 0034489068     PISSN: 13816810     EISSN: None     Source Type: Journal    
DOI: 10.1076/1381-6810(200012)2141-HFT211     Document Type: Article

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