Epigenetics in congenital diseases and pervasive developmental disorders
スポンサーリンク
概要
- 論文の詳細を見る
- 2008-01-01
著者
-
KUBOTA Takeo
Department of Mental Retardation and Birth Defect Research, National Institute of Neuroscience, Nati
-
Kubota Takeo
Department Of Epigenetics Medicine Interdisciplinary Graduate School Of Medicine And Engineering Uni
-
Kubota Takeo
Department Of Epigenetic Medicine Interdisciplinary Graduate School Of Medicine And Engineering University Of Yamanashi
関連論文
- Familial 14-Mb deletion at 21q11.2-q21.3 and variable phenotypic expression
- Mutational Analysis of the WASP Gene in 2 Korean Families with Wiskott-Aldrich Syndrome
- Clinical applications of two-color telomeric fluorescence in situ hybridization for prenatal diagnosis : Identification of chromosomal translocation in five families with recurrent miscarriages or a child with multiple congenital anomalies
- A new assay for the analysis of X-chromosome inactivation in carriers with an X-linked disease
- Epigenetics in congenital diseases and pervasive developmental disorders
- Novel Etiological and Therapeutic Strategies for Neurodiseases: Epigenetic Understanding of Gene–Environment Interactions
- Novel Etiological and Therapeutic Strategies for Neurodiseases : Epigenetic Understanding of Gene-Environment Interactions
- Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis
- Adult Onset X-Linked Chronic Granulomatous Disease in a Woman Patient Caused by a de novo Mutation in Paternal-Origin CYBB Gene and Skewed Inactivation of Normal Maternal X Chromosome
- Epigenomics comes of age with expanding roles inbiological understanding and clinical application