PDF) Prevalence of Immunological Defects in a Cohort of 97 Rubinstein–Taybi Syndrome Patients
Por um escritor misterioso
Descrição

Frontiers Gut dysmotility in children with neurological

Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With

KMT2C/D COMPASS complex-associated diseases [KCDCOM-ADs]: an

Cells, Free Full-Text

Novel heterozygous variants in the EP300 gene cause Rubinstein

Identification of 22q11.2 deletion in a patient with schizophrenia

Disease Progression of WHIM Syndrome in an International Cohort of

A guide for the diagnosis of rare and undiagnosed disease: beyond

Genetic Syndromes with Evidence of Immune Deficiency - ScienceDirect

High frequency of copy number imbalances in Rubinstein–Taybi

PDF) Rubinstein-Taybi Syndrome: A Case Report
de
por adulto (o preço varia de acordo com o tamanho do grupo)