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rubinstein taybi omim
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
About - DECIPHER v11.23
IJMS, Free Full-Text
Subclass IgG levels of patients with Rubinstein-Taybi syndrome compared
Rubinstein-Taybi Syndrome 1
PDF) Rubinstein-Taybi syndrome medical guidelines
Novel cAMP binding protein-BP (CREBBP) mutation in a girl with Rubinstein- Taybi syndrome, GH deficiency, Arnold Chiari malformation and pituitary hypoplasia – topic of research paper in Clinical medicine. Download scholarly article PDF
Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein– Taybi and Filippi syndromes
Rubinstein–Taybi syndrome European Journal of Human Genetics
Congenital glaucoma as a presenting feature of Rubinstein-Taybi
Rubinstein–Taybi syndrome associated with Chiari type I malformation caused by a large 16p13.3 microdeletion: A contiguous gene syndrome? - Wójcik - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library
Rubinstein-Taybi Syndrome OMIM# 180849 - FDNA™
Chemical and genetic rescue of an ep300 knockdown model for Rubinstein Taybi Syndrome in zebrafish - ScienceDirect
Rubinstein-Taybi syndrome: Dental manifestations and management
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
Rubinstein-Taybi syndrome - wikidoc
Forgotten Diseases Research Foundation
OMIM diseases as a function of associated HPO phenotypes. Data include
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations - Van‐Gils - 2019 - Clinical Genetics - Wiley Online Library
First case report of inherited Rubinstein-Taybi syndrome associated with a novel EP300 variant – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open
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