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J Med Genet ; 28(4): 277-9, 1991 Apr.
Article in English | MEDLINE | ID: mdl-1856836

ABSTRACT

Two sibs with a phenotype characterised by short stature, brachydactyly, and ocular anomalies (Peters' anomaly) are reported (Peters'-plus syndrome). The consanguinity is in agreement with the proposed autosomal recessive inheritance.


Subject(s)
Cornea/abnormalities , Genes, Recessive , Growth Disorders/genetics , Child, Preschool , Consanguinity , Female , Humans , Infant , Male , Phenotype , Syndrome
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