Congenital cataracts - facial dysmorphism - neuropathy

Orphanet Journal of Rare Diseases

Volumn 1, Issue 1, 2006, Pages

  Kalaydjieva, Luba ^a  

^a UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXY TERMINAL DOMAIN PHOSPHATASE; CARBOXY-TERMINAL DOMAIN PHOSPHATASE; PHOSPHOPROTEIN PHOSPHATASE;

CATARACT; CHROMOSOME 18; CONGENITAL MALFORMATION; FACE; FACIAL NERVE DISEASE; GENETICS; GIPSY; HUMAN; MULTIPLE MALFORMATION SYNDROME; MUTATION; PATHOLOGY; REVIEW;

ABNORMALITIES, MULTIPLE; CATARACT; CHROMOSOMES, HUMAN, PAIR 18; FACE; FACIAL NERVE DISEASES; GYPSIES; HUMANS; MUTATION; PHOSPHOPROTEIN PHOSPHATASE;

EID: 34248211323     PISSN: None     EISSN: 17501172     Source Type: Journal    
DOI: 10.1186/1750-1172-1-32     Document Type: Review

References (18)

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