Mutations in SRCAP, Encoding SNF2-Related CREBBP Activator Protein, Cause Floating-Harbor Syndrome - ScienceDirect
Por um escritor misterioso
Descrição
Floating-Harbor syndrome (FHS) is a rare condition characterized by short stature, delayed osseous maturation, expressive-language deficits, and a dis…
ACTB Loss-of-Function Mutations Result in a Pleiotropic Developmental Disorder - ScienceDirect
Mutations in SRCAP, encoding SNF2-related CREBBP activator protein, cause Floating-Harbor syndrome.
Rare and undiagnosed diseases: From disease-causing gene identification to mechanism elucidation - ScienceDirect
PDF) Mutations in SRCAP, encoding SNF2-related CREBBP activator protein, cause Floating-Harbor syndrome
Znhit1 controls meiotic initiation in male germ cells by coordinating with Stra8 to activate meiotic gene expression - ScienceDirect
Mutations in PIK3R1 Cause SHORT Syndrome - ScienceDirect
PDF) Mutations in SRCAP, encoding SNF2-related CREBBP activator protein, cause Floating-Harbor syndrome
16p11.2 de novo microdeletion encompassing SRCAP gene in a patient with speech impairment, global developmental delay and behavioural problems - ScienceDirect
The Human SRCAP Chromatin Remodeling Complex Promotes DNA-End Resection - ScienceDirect
Frontiers Molecular Genetics and Pathogenesis of the Floating Harbor Syndrome: Case Report of Long-Term Growth Hormone Treatment and a Literature Review
PDF) Mutations in SRCAP, encoding SNF2-related CREBBP activator protein, cause Floating-Harbor syndrome
Generation of two iPSC lines (MHHi001-A-12 and MHHi001-A-13) carrying biallelic truncating mutations at the 3′-end of SRCAP using CRISPR/Cas9 - ScienceDirect
De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures - ScienceDirect
de
por adulto (o preço varia de acordo com o tamanho do grupo)
:quality(75)/cloudfront-us-east-1.images.arcpublishing.com/elcomercio/EY5E5KE4Z5AZJCX2QTDOEDEY3Q.jpg)
