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Barrett's Esophagus in Rubinstein-Taybi Syndrome

Rubinstein-Taybi syndrome (RSTS; Online Mendelian Inheritance in Man(® )[OMIM(®)] #180849, #613684; Orpha: 783 ) is a rare plurimalformative autosomal dominant genetic disorder that affects one in 100,000-125,000 newborns with equal male and female distribution. It is characterized by distinctive fa...

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Detalles Bibliográficos
Autores principales:	Kumar, Prabhat, Thota, Prashanthi N
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Cureus 2020
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7769793/ https://www.ncbi.nlm.nih.gov/pubmed/33391942 http://dx.doi.org/10.7759/cureus.11709

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