PDF) An unusual presentation of Rubinstein-Taybi Syndrome with bilateral postaxial polydactyly Corresponding author
Por um escritor misterioso
Last updated 28 março 2025

Rubinstein-Taybi Syndrome (RSTS) is a rare multiple congenital anomaly syndrome. Only 250 cases have been described in medical literature. We hereby present a 10-month-old male child with characteristic facial features and hand and feet anomalies.

Rubinstein–Taybi syndrome in diverse populations - Tekendo

PDF) Lacrimal drainage anomalies in Rubinstein-Taybi syndrome

Mosaic CREBBP mutation causes overlapping clinical features of

PDF) Lacrimal drainage anomalies in Rubinstein-Taybi syndrome

PDF] Rubinstein-Taybi Syndrome: A Case Report

Molecular studies in 10 cases of Rubinstein-Taybi syndrome

Chiari 1 malformation and exome sequencing in 51 trios: the

PDF) Anophthalmia with cleft palate and micrognathia: A new

PDF) Rubinstein-Taybi syndrome: a rare case report of a female

PDF) Lacrimal drainage anomalies in Rubinstein-Taybi syndrome

PDF) Lacrimal drainage anomalies in Rubinstein-Taybi syndrome

PDF) Lacrimal drainage anomalies in Rubinstein-Taybi syndrome

An unusual presentation of Rubinstein-Taybi Syndrome with
Recomendado para você
-
Rubinstein-Taybi Syndrome: A Complete Overview — DermNet28 março 2025
-
Forgotten Diseases Research Foundation28 março 2025
-
Rubinstein Taybi Syndrome: Most Up-to-Date Encyclopedia, News & Reviews28 março 2025
-
Figure 1. [Facial appearance of a girl age 11 years with FHS (SRCAP pathogenic variant p.Arg2444Ter)]. - GeneReviews® - NCBI Bookshelf28 março 2025
-
Robinow Syndrome: Most Up-to-Date Encyclopedia, News & Reviews28 março 2025
-
Mutations in SRCAP, Encoding SNF2-Related CREBBP Activator Protein, Cause Floating-Harbor Syndrome - ScienceDirect28 março 2025
-
Silver Russell Syndrome: Most Up-to-Date Encyclopedia, News & Reviews28 março 2025
-
What is CdLS? Ben and his Brothers: Life with 4 boys and CdLS28 março 2025
-
Somatic and germ‐line mosaicism in Rubinstein–Taybi syndrome - Chiang - 2009 - American Journal of Medical Genetics Part A - Wiley Online Library28 março 2025
-
Expanding the phenotype associated to KMT2A variants: overlapping clinical signs between Wiedemann–Steiner and Rubinstein–Taybi syndromes28 março 2025
você pode gostar
-
Se liga no recado da atleta Gabriela Saltarelli, campeã mundial28 março 2025
-
Retinal Detachment NYC - Vitreous Retina Macula Consultants of New28 março 2025
-
Initial D' Watch Order: Chronological & Release Date28 março 2025
-
Download Starblast android on PC28 março 2025
-
Argentina Superliga | 2022 Ferrocarril Oeste Home Jersey28 março 2025
-
How to Draw Dragon Ball Z: Pro Edition28 março 2025
-
Papa's Hot Doggeria To Go!::Appstore for Android28 março 2025
-
Monkey Mart 3º Store Poki Games28 março 2025
-
April 27 to May 4 - THE CROWN LETTER28 março 2025
-
YARN, Video gifs by quotes, afcad3e028 março 2025