Rubenstein-Taybi Syndrome April is diagnosed with Rubinstein
Por um escritor misterioso
Descrição
April is diagnosed with Rubinstein-Taybi syndrome. She is nonverbal and not yet able to communicate verbally. Her sister, Rachel, is studying to become a
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Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With Multiplex Ligation-Dependent Probe Amplification (MLPA) and Whole-Exome Sequencing (WES): Case Series With a Novel CREBBP Variant
What I've Learned As A Sibling Of Someone With Special Needs
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Ultrasound 2-D and 3-D diagnosis of Rubinstein–Taybi syndrome in a 21-week-old fetus
![Rubenstein-Taybi Syndrome April is diagnosed with Rubinstein](https://i1.rgstatic.net/publication/271223834_Rubinstein-Taybi_syndrome_Clinical_features_genetic_basis_diagnosis_and_management/links/54d25a210cf28e069723ee05/largepreview.png)
PDF) Rubinstein-Taybi syndrome: Clinical features, genetic basis, diagnosis, and management
![Rubenstein-Taybi Syndrome April is diagnosed with Rubinstein](https://3.bp.blogspot.com/-ehjgsaHwpc0/Wx2SCOnSewI/AAAAAAAABsk/H2GBhe6GeHorb8-fWQf9gert3STwYa4JgCLcBGAs/w1200-h630-p-k-no-nu/RTS-Conference_09-Jun-2018.jpg)
Rubinstein-Taybi Syndrome: UK RTS Support Group Conference on 9th June 2018
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Rubinstein–Taybi syndrome European Journal of Human Genetics
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Genes, Free Full-Text
![Rubenstein-Taybi Syndrome April is diagnosed with Rubinstein](http://faoj.org/wp-content/uploads/2008/06/rstsfig1b.jpg)
Rubinstein-Taybi Syndrome: A case report
![Rubenstein-Taybi Syndrome April is diagnosed with Rubinstein](https://www.frontiersin.org/files/Articles/848879/fgene-13-848879-HTML-r1/image_m/fgene-13-848879-g001.jpg)
Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With Multiplex Ligation-Dependent Probe Amplification (MLPA) and Whole-Exome Sequencing (WES): Case Series With a Novel CREBBP Variant
![Rubenstein-Taybi Syndrome April is diagnosed with Rubinstein](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fejhg.2010.121/MediaObjects/41431_2011_Article_BFejhg2010121_Fig1_HTML.jpg)
Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein –Taybi syndrome detected by aCGH
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Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
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