Peripheral retinopathy in offspring of carriers of norrie disease gene mutations: Possible transplacental effect of abnormal norrin

Ophthalmology

Volumn 103, Issue 12, 1996, Pages 2128-2134

  Mintz Hittner, H A ^a   Ferrell, R E ^a   Sims, K B ^a   Fernandez, K M ^a   Gemmell, B S ^a   Satriano, D R ^a   Caster, J ^a   Kretzer, F L ^a  

^a NONE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; FAMILY STUDY; FEMALE; GENE MUTATION; HETEROZYGOTE; HUMAN; MAJOR CLINICAL STUDY; MALE; NORRIE DISEASE; PRIORITY JOURNAL; PROGENY; RETINA DETACHMENT; RETINOPATHY; RETROLENTAL FIBROPLASIA; VITREORETINOPATHY; X CHROMOSOME LINKED DISORDER;

EID: 0030458819     PISSN: 01616420     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0161-6420(96)30379-5     Document Type: Article

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