MECP2 abnormality phenotypes: clinicopathologic area with broad variability.
about
Genetics evaluation for the etiologic diagnosis of autism spectrum disordersThe genetics of autistic disorders and its clinical relevance: a review of the literatureEmerging pharmacotherapies for neurodevelopmental disordersA review of Rett syndrome (RTT) with induced pluripotent stem cellsClinical genetic testing for patients with autism spectrum disordersClinical genetics evaluation in identifying the etiology of autism spectrum disorders.Pharmacology and genetics of autism: implications for diagnosis and treatment.Genetic diseases: congenital central hypoventilation, Rett, and Prader-Willi syndromes.A novel hypomorphic MECP2 point mutation is associated with a neuropsychiatric phenotype.Early motor phenotype detection in a female mouse model of Rett syndrome is improved by cross-fostering.Phenotypic and genotypic variability in four males with MECP2 gene sequence aberrations including a novel deletion.Early infantile onset ''congenital'' Rett syndrome variants: Swedish experience through four decades and mutation analysis.
P2860
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P2860
MECP2 abnormality phenotypes: clinicopathologic area with broad variability.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
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2005年學術文章
@zh-hant
name
MECP2 abnormality phenotypes: clinicopathologic area with broad variability.
@ast
MECP2 abnormality phenotypes: clinicopathologic area with broad variability.
@en
type
label
MECP2 abnormality phenotypes: clinicopathologic area with broad variability.
@ast
MECP2 abnormality phenotypes: clinicopathologic area with broad variability.
@en
prefLabel
MECP2 abnormality phenotypes: clinicopathologic area with broad variability.
@ast
MECP2 abnormality phenotypes: clinicopathologic area with broad variability.
@en
P2860
P1476
MECP2 abnormality phenotypes: clinicopathologic area with broad variability.
@en
P2093
Anna Erlandson
P2860
P304
P356
10.1177/08830738050200090501
P577
2005-09-01T00:00:00Z