Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein– Taybi and Filippi syndromes
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PDF) Case Report: Low-Level Maternal Mosaicism of a Novel CREBBP
Further delineation of an entity caused by CREBBP and EP300
Mosaic CREBBP mutation causes overlapping clinical features of
Epigenetic mechanisms of Rubinstein-Taybi syndrome. - Abstract
Epigenetic mechanisms of Rubinstein-Taybi syndrome. - Abstract
PDF) Case Report: Low-Level Maternal Mosaicism of a Novel CREBBP
Clinical relevance of postzygotic mosaicism in Cornelia de Lange
Microdeletions and mutations of CREBBP (CBP) gene can cause
Rubinstein–Taybi syndrome in diverse populations - Tekendo
Diagnosis and management of Cornelia de Lange syndrome: first
PDF] Multiple Dental and Skeletal Abnormalities in an Individual
Articles in 2016 European Journal of Human Genetics
Figure 1 from Mutations in CKAP2L, the human homolog of the mouse
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Figure 1 from Mutations in CKAP2L, the human homolog of the mouse
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