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Short stature, brachydactyly, and Peters' anomaly (Peters'-plus syndrome): confirmation of autosomal recessive inheritance.
J C JC de Almeida, D F DF Reis, J J Llerena Júnior, J J Barbosa Neto, R L RL Pontes, S S Middleton and L F LF Telles
J Med Genet 28(4):277-9 (1991)
PMID 1856836
PMCID: 1016833
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.
DOI:
Version: za2963e q8za6 q8zb3 q8zc7 q8zdd q8ze6 q8zfe q8zg4
DOI:
Version: za2963e q8za6 q8zb3 q8zc7 q8zdd q8ze6 q8zfe q8zg4