PDF) Rubinstein–Taybi syndrome (CREBBP, EP300) Martine van Belzen and Oliver Bartsch

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PDF) Rubinstein–Taybi syndrome (CREBBP, EP300)  Martine van Belzen and  Oliver Bartsch
PDF) Rubinstein-Taybi syndrome: Clinical profile of 11 patients and review of literature
PDF) Rubinstein–Taybi syndrome (CREBBP, EP300)  Martine van Belzen and  Oliver Bartsch
PDF) Rubinstein–Taybi syndrome: New neuroradiological and neuropsychiatric insights from a multidisciplinary approach
PDF) Rubinstein–Taybi syndrome (CREBBP, EP300)  Martine van Belzen and  Oliver Bartsch
Rubinstein–Taybi syndrome (CREBBP, EP300)
PDF) Rubinstein–Taybi syndrome (CREBBP, EP300)  Martine van Belzen and  Oliver Bartsch
PDF) Rubinstein-Taybi syndrome medical guidelines
PDF) Rubinstein–Taybi syndrome (CREBBP, EP300)  Martine van Belzen and  Oliver Bartsch
PDF) Nephrotic syndrome in a case of Rubinstein Taybi syndrome: a rare case report
PDF) Rubinstein–Taybi syndrome (CREBBP, EP300)  Martine van Belzen and  Oliver Bartsch
PDF) Nephrotic syndrome in a case of Rubinstein Taybi syndrome: a rare case report
PDF) Rubinstein–Taybi syndrome (CREBBP, EP300)  Martine van Belzen and  Oliver Bartsch
Rubinstein–Taybi syndrome (CREBBP, EP300)
PDF) Rubinstein–Taybi syndrome (CREBBP, EP300)  Martine van Belzen and  Oliver Bartsch
Oliver BARTSCH, Medical Doctor, Professor, Universitätsmedizin der Johannes Gutenberg-Universität Mainz, Mainz, Institute of Human Genetics
PDF) Rubinstein–Taybi syndrome (CREBBP, EP300)  Martine van Belzen and  Oliver Bartsch
PDF) Rubinstein-Taybi syndrome in a Saudi boy with distinct features and variants in both the CREBBP and EP300 genes: A case report
PDF) Rubinstein–Taybi syndrome (CREBBP, EP300)  Martine van Belzen and  Oliver Bartsch
PDF) CREBBP and EP300 mutational spectrum and clinical presentations in a cohort of Swedish patients with Rubinstein–Taybi syndrome
PDF) Rubinstein–Taybi syndrome (CREBBP, EP300)  Martine van Belzen and  Oliver Bartsch
PDF) Case Report: Low-Level Maternal Mosaicism of a Novel CREBBP Variant Causes Recurrent Rubinstein-Taybi Syndrome in Two Siblings of a Chinese Family
PDF) Rubinstein–Taybi syndrome (CREBBP, EP300)  Martine van Belzen and  Oliver Bartsch
PDF) CREBBP and EP300 mutational spectrum and clinical presentations in a cohort of Swedish patients with Rubinstein–Taybi syndrome
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