A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3

Human Molecular Genetics

Volumn 5, Issue 6, 1996, Pages 843-847

  Sertie A L ^a   Quimby, M ^b   Moreira, E S ^a   Murray, J ^b   Zatz, M ^a   Antonarakis, S E ^c   Passos Bueno, M R ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

^b UNIVERSITY OF IOWA   (United States)

^c UNIVERSITY OF GENEVA   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BRAZIL; CHROMOSOME 21Q; ENCEPHALOCELE; GENE; GENE LOCATION; GENE MAPPING; HIGH MYOPIA; HUMAN; OCCIPITAL CORTEX; PRIORITY JOURNAL; RETINA DETACHMENT; VITREORETINAL DEGENERATION;

ABNORMALITIES, MULTIPLE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 21; ENCEPHALOCELE; FEMALE; HAPLOTYPES; HUMANS; LINKAGE (GENETICS); MALE; OCCIPITAL BONE; PEDIGREE; RETINAL DISEASES; SYNDROME;

EID: 0029977272     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/5.6.843     Document Type: Article

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