Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein– Taybi and Filippi syndromes
Por um escritor misterioso
Descrição
Short Report European Journal of Human Genetics
Microdeletions and mutations of CREBBP (CBP) gene can cause
Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian
PDF] Multiple Dental and Skeletal Abnormalities in an Individual
Rubinstein–Taybi syndrome in diverse populations - Tekendo
Glen MONROE, Postdoc, PhD
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Frontiers Case report: A preterm infant with rubinstein-taybi
Figure 1 from Mutations in CKAP2L, the human homolog of the mouse
A Novel CREBBP in-Frame Deletion Variant in a Chinese Girl with
de
por adulto (o preço varia de acordo com o tamanho do grupo)