标题
Fragile X Syndrome: The FMR1 CGG Repeat Distribution Among World Populations
作者
关键词
-
出版物
ANNALS OF HUMAN GENETICS
Volume 76, Issue 2, Pages 178-191
出版商
Wiley
发表日期
2011-12-21
DOI
10.1111/j.1469-1809.2011.00694.x
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Treatment of fragile X-associated tremor ataxia syndrome (FXTAS) and related neurological problems
- (2016) Randi Hagerman Clinical Interventions in Aging
- Decreased Fragile X Mental Retardation Protein Expression Underlies Amygdala Dysfunction in Carriers of the Fragile X Premutation
- (2011) David Hessl et al. BIOLOGICAL PSYCHIATRY
- CGG repeat in the FMR1 gene: size matters
- (2011) R Willemsen et al. CLINICAL GENETICS
- Initiation of Translation of the FMR1 mRNA Occurs Predominantly through 5′-End-Dependent Ribosomal Scanning
- (2011) Anna L. Ludwig et al. JOURNAL OF MOLECULAR BIOLOGY
- Differential usage of transcriptional start sites and polyadenylation sites in FMR1 premutation alleles
- (2011) F. Tassone et al. NUCLEIC ACIDS RESEARCH
- Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males
- (2010) Stephen C. Collins et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Genetic Diversity of the Fragile X Syndrome Gene (FMR1) in a Large Sub-Saharan West African Population
- (2010) Emmanuel K. Peprah et al. ANNALS OF HUMAN GENETICS
- Gene Expression Profiling Identifies WNT7A As a Possible Candidate Gene for Decreased Cancer Risk in Fragile X Syndrome Patients
- (2010) Mónica Alejandra Rosales-Reynoso et al. ARCHIVES OF MEDICAL RESEARCH
- A systematic review of population screening for fragile X syndrome
- (2010) Melissa K Hill et al. GENETICS IN MEDICINE
- Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio
- (2010) David Eugeny Godler et al. HUMAN MOLECULAR GENETICS
- Mechanisms of trinucleotide repeat instability during human development
- (2010) Cynthia T. McMurray NATURE REVIEWS GENETICS
- Incidence of Fragile X Syndrome by Newborn Screening for Methylated FMR1 DNA
- (2009) Bradford Coffee et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Microsatellite repeat instability and neurological disease
- (2009) Judith R. Brouwer et al. BIOESSAYS
- Fragile X carrier screening and FMR1 allele distribution in the Japanese population
- (2009) Susumu Otsuka et al. BRAIN & DEVELOPMENT
- Fragile X syndrome screening of families with consanguineous and non-consanguineous parents in the Iranian population
- (2009) Ali Reza Pouya et al. European Journal of Medical Genetics
- Haplotype and AGG Interspersion Analysis of FMR1 Alleles in a Croatian Population: No Founder Effect Detected in Patients with Fragile X Syndrome
- (2009) H. Đokić et al. HUMAN BIOLOGY
- A Review of Fragile X Premutation Disorders
- (2009) James A. Bourgeois et al. JOURNAL OF CLINICAL PSYCHIATRY
- The AGG interruption pattern within the CGG repeat of the FMR1 gene among Taiwanese population
- (2009) Hua-Hsien Chiu et al. JOURNAL OF GENETICS
- Examination of FMR1 transcript and protein levels among 74 premutation carriers
- (2009) Emmanuel Peprah et al. JOURNAL OF HUMAN GENETICS
- The nucleotide binding dynamics of human MSH2–MSH3 are lesion dependent
- (2009) Barbara A L Owen et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- ATM and ATR protect the genome against two different types of tandem repeat instability in Fragile X premutation mice
- (2009) A. Entezam et al. NUCLEIC ACIDS RESEARCH
- MSH2 ATPase Domain Mutation Affects CTG•CAG Repeat Instability in Transgenic Mice
- (2009) Stéphanie Tomé et al. PLoS Genetics
- Genetic variation of theFMR1 gene among four Mexican populations: Mestizo, Huichol, Purepecha, and Tarahumara
- (2008) Patricio Barros-Núñez et al. AMERICAN JOURNAL OF HUMAN BIOLOGY
- Reproductive Health of Adolescent Girls Who Carry the FMR1 Premutation
- (2008) John J. De Caro et al. Annals of the New York Academy of Sciences
- Reduced Hippocampal Activation During Recall is Associated with Elevated FMR1 mRNA and Psychiatric Symptoms in Men with the Fragile X Premutation
- (2008) Kami Koldewyn et al. Brain Imaging and Behavior
- Features of trinucleotide repeat instability in vivo
- (2008) Irina V Kovtun et al. CELL RESEARCH
- Clinical significance of tri-nucleotide repeats in Fragile X testing: A clarification of American College of Medical Genetics guidelines
- (2008) Kathryn E Kronquist et al. GENETICS IN MEDICINE
- Prevalence of the Fragile X Syndrome Among Estonian Mentally Retarded and the Entire Children's Population
- (2008) Helen Puusepp et al. JOURNAL OF CHILD NEUROLOGY
- Fragile X Syndrome in Korea: A Case Series and a Review of the Literature
- (2008) Shin-Young Yim et al. JOURNAL OF KOREAN MEDICAL SCIENCE
- Fragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and Function
- (2008) Gary J. Bassell et al. NEURON
- Inherited Susceptibility to Common Cancers
- (2008) William D. Foulkes NEW ENGLAND JOURNAL OF MEDICINE
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