Rubinstein-Taybi Syndrome OMIM# 180849 - FDNA™
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Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel
PDF) Clinical exome sequencing identifies novel CREBBP variants in
Rubinstein‐Taybi syndrome in Chinese population with four novel
Clinical exome sequencing identifies novel CREBBP variants in 18
Genetic Syndromes with Evidence of Immune Deficiency - ScienceDirect
Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With
Rubinstein-Taybi syndrome: clinical features, genetic basis
Rubinstein-Taybi Syndrome OMIM# 180849 - FDNA™
Cureus Whole-Exome Sequencing Identified a Novel DYRK1A Variant
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