Low-normal FMR1 CGG repeat length: phenotypic associations. - Wikidata - awgldk - TriplyDB

Low-normal FMR1 CGG repeat length: phenotypic associations.

Low-normal FMR1 CGG repeat length: phenotypic associations.

http://www.wikidata.org/entity/Q34153985

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Distribution of the FMR1 gene in females by race/ethnicity: women with diminished ovarian reserve versus women with normal fertility (SWAN study).FMR1 CGG Repeats: Reference Levels and Race-Ethnic Variation in Women With Normal Fertility (Study of Women's Health Across the Nation).Fragile X syndrome: a review of clinical and molecular diagnoses.Human pluripotent stem cell models of Fragile X syndrome.Is Low FMR1 CGG Repeat Length in Males Correlated with Family History of BRCA-Associated Cancers? An Exploratory Analysis of Medical Records.The impact of FMR1 gene mutations on human reproduction and development: a systematic review.Reduction in the number of CGG repeats on the FMR1 gene in carriers of genetic disorders versus noncarriers.Stem Cell Technology for (Epi)genetic Brain Disorders.FMR1 genotype interacts with parenting stress to shape health and functional abilities in older age.Curvilinear Association Between Language Disfluency and CGG Repeat Size Across the Normal, Intermediate, and Premutation Range

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P2860

Low-normal FMR1 CGG repeat length: phenotypic associations.

http://www.wikidata.org/entity/Q34153985

description

2014 nî lūn-bûn

@nan

2014 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2014年の論文

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2014年論文

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2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

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2014年论文

@wuu

name

Low-normal FMR1 CGG repeat length: phenotypic associations.

@ast

Low-normal FMR1 CGG repeat length: phenotypic associations.

@en

Low-normal FMR1 CGG repeat length: phenotypic associations.

@nl

type

label

Low-normal FMR1 CGG repeat length: phenotypic associations.

@ast

Low-normal FMR1 CGG repeat length: phenotypic associations.

@en

Low-normal FMR1 CGG repeat length: phenotypic associations.

@nl

prefLabel

Low-normal FMR1 CGG repeat length: phenotypic associations.

@ast

Low-normal FMR1 CGG repeat length: phenotypic associations.

@en

Low-normal FMR1 CGG repeat length: phenotypic associations.

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FGENE.2014.00309

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Frontiers in Genetics

P1476

Low-normal FMR1 CGG repeat length: phenotypic associations.

@en

P2093

Jan S Greenberg

http://www.w3.org/2001/XMLSchema#string

Jinkuk Hong

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Leann Smith

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Marsha R Mailick

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Matthew Maenner

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Mei W Baker

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Paul Rathouz

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P2860

The fragile-X premutation: a maturing perspective.

Fragile X syndrome: loss of local mRNA regulation alters synaptic development and function

Technical standards and guidelines for fragile X: the first of a series of disease-specific supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics. Quality Assurance Subcommittee of

Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox

Quality and quantity of saliva DNA obtained from the self-administrated oragene method--a pilot study on the cohort of Swedish men

FMR1 CGG allele size and prevalence ascertained through newborn screening in the United States

Depression and anxiety in women with early breast cancer: five year observational cohort study.

The (CGG)n repeat element within the 5' untranslated region of the FMR1 message provides both positive and negative cis effects on in vivo translation of a downstream reporter.

BRCA1/2 mutations appear embryo-lethal unless rescued by low (CGG n<26) FMR1 sub-genotypes: explanation for the "BRCA paradox"?

Analysis of a CGG sequence at the FMR-1 locus in fragile X families and in the general population.

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309

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scholarly article

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10.3389/FGENE.2014.00309

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5

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2014-09-09T00:00:00Z

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266086350

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25250047

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4158814

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