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Two cases of Temple–Baraitser syndrome: natural history and further delineation of the clinical and radiologic phenotypes

This study reports on two individuals with Temple–Baraitser syndrome, manifesting typical hallux and pollex findings, global developmental delay, and seizures. In the five previous cases identified to date, consistent craniofacial and osseous characteristics have been observed. The children describe...

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Detalles Bibliográficos
Publicado en:Clin Dysmorphol
Autor principal: Shen, Joseph J.
Formato: Artigo
Lenguaje:Inglês
Publicado: Lippincott Williams & Wilkins 2015
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4345968/
https://ncbi.nlm.nih.gov/pubmed/25629734
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MCD.0000000000000072
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