Short stature, brachydactyly, and Peters' anomaly (Peters'-plus syndrome): confirmation of autosomal recessive inheritance.

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.

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Hlavní autoři: de Almeida, J C, Reis, D F, Llerena Júnior, J, Barbosa Neto, J, Pontes, R L, Middleton, S, Telles, L F
Médium: Artigo
Jazyk:Inglês
Vydáno: 1991
Témata:
Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1016833/
https://ncbi.nlm.nih.gov/pubmed/1856836
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