High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis
Por um escritor misterioso
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![High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis](https://media.springernature.com/m685/springer-static/image/art%3A10.1007%2Fs00439-015-1542-9/MediaObjects/439_2015_1542_Fig3_HTML.gif)
Characterization of 14 novel deletions underlying Rubinstein–Taybi syndrome: an update of the CREBBP deletion repertoire
![High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis](https://static.cambridge.org/binary/version/id/urn:cambridge.org:id:binary-alt:20160710080711-69140-mediumThumb-S1462399410001390_fig3g.jpg?pub-status=live)
The clinical context of copy number variation in the human genome, Expert Reviews in Molecular Medicine
![High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis](https://media.springernature.com/m685/springer-static/image/art%3A10.1007%2Fs00439-015-1542-9/MediaObjects/439_2015_1542_Fig2_HTML.gif)
Characterization of 14 novel deletions underlying Rubinstein–Taybi syndrome: an update of the CREBBP deletion repertoire
![High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis](https://0.academia-photos.com/attachment_thumbnails/74496282/mini_magick20211110-2130-82fw1w.png?1636564977)
PDF) Nephrotic syndrome in a case of Rubinstein Taybi syndrome: a rare case report
![High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis](https://onlinelibrary.wiley.com/cms/asset/2e25c837-deeb-40df-8f31-7a4bd9b0fb5d/ajmga61888-fig-0001-m.jpg)
Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
![High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis](https://0.academia-photos.com/attachment_thumbnails/41232762/mini_magick20190219-22204-suhuj4.png?1550624942)
PDF) New dysmorphic features in Rubinstein-Taybi syndrome
![High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis](https://0.academia-photos.com/attachment_thumbnails/46869565/mini_magick20190208-12281-elgzif.png?1549658922)
PDF) New dysmorphic features in Rubinstein-Taybi syndrome
![High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis](https://www.frontiersin.org/files/Articles/848879/fgene-13-848879-HTML-r1/image_m/fgene-13-848879-g003.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
![High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis](https://0.academia-photos.com/attachment_thumbnails/93512303/mini_magick20221102-1-8r0kup.png?1667374157)
PDF) New mutation of Rubinstein-Taybi Syndrome
![High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis](https://ars.els-cdn.com/content/image/1-s2.0-S0896841121001177-gr6.jpg)
Individual functions of the histone acetyl transferases CBP and p300 in regulating the inflammatory response of synovial fibroblasts - ScienceDirect
![High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis](https://media.springernature.com/m685/springer-static/image/art%3A10.1186%2F1471-2350-7-77/MediaObjects/12881_2006_Article_185_Fig5_HTML.jpg)
Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian patients, BMC Medical Genetics
![High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis](https://onlinelibrary.wiley.com/cms/asset/1e14f96d-b018-49bd-9289-035655527dbd/mgg31009-fig-0002-m.jpg)
Clinical exome sequencing identifies novel CREBBP variants in 18 Chinese Rubinstein–Taybi Syndrome kids with high frequency of polydactyly - Yu - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
![High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis](https://onlinelibrary.wiley.com/cms/asset/219453ee-7715-4224-86aa-0868af19ee0d/cge13493-toc-0001-m.jpg?trick=1700875205935)
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations - Van‐Gils - 2019 - Clinical Genetics - Wiley Online Library
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