Population-based estimates of the prevalence of FMR1 expansion mutations in women with early menopause and primary ovarian insufficiency. - Test2 - elhamkhani - TriplyDB

Population-based estimates of the prevalence of FMR1 expansion mutations in women with early menopause and primary ovarian insufficiency.

Population-based estimates of the prevalence of FMR1 expansion mutations in women with early menopause and primary ovarian insufficiency.

http://www.wikidata.org/entity/Q37555606

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Repeat-mediated genetic and epigenetic changes at the FMR1 locus in the Fragile X-related disorders The FMR1 gene, infertility, and reproductive decision-making: a review Development of Genetic Testing for Fragile X Syndrome and Associated Disorders, and Estimates of the Prevalence of FMR1 Expansion Mutations Study of the Genetic Etiology of Primary Ovarian Insufficiency: FMR1 Gene 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).FMR1 premutation is an uncommon explanation for premature ovarian failure in Han Chinese.Dynamics of the ovarian reserve and impact of genetic and epidemiological factors on age of menopause.Evidence of an age-related correlation of ovarian reserve and FMR1 repeat number among women with "normal" CGG repeat status.Towards a Better Molecular Diagnosis of FMR1-Related Disorders-A Multiyear Experience from a Reference Lab.Current concepts in premature ovarian insufficiency.Molecular insights into the aetiology of female reproductive ageing.Distribution of FMR1 and FMR2 Repeats in Argentinean Patients with Primary Ovarian Insufficiency.Hormone replacement therapy in young women with primary ovarian insufficiency and early menopause.Diminished ovarian reserve is not observed in infertility patients with high normal CGG repeats on the fragile X mental retardation 1 (FMR1) gene.Premature Ovarian Insufficiency - an update on recent advances in understanding and management.Reproductive ovarian testing and the alphabet soup of diagnoses: DOR, POI, POF, POR, and FOR.Ovarian Follicular Theca Cell Recruitment, Differentiation, and Impact on Fertility: 2017 Update.Association between fragile X premutation and premature ovarian failure: a case-control study and meta-analysis.Menstrual Cycle Hormone Changes Associated with Reproductive Aging and How They May Relate to Symptoms

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Population-based estimates of the prevalence of FMR1 expansion mutations in women with early menopause and primary ovarian insufficiency.

http://www.wikidata.org/entity/Q37555606

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 23 May 2013

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Population-based estimates of ...... primary ovarian insufficiency.

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Population-based estimates of ...... primary ovarian insufficiency.

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Population-based estimates of ...... primary ovarian insufficiency.

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Population-based estimates of ...... primary ovarian insufficiency.

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Population-based estimates of ...... primary ovarian insufficiency.

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Population-based estimates of ...... primary ovarian insufficiency.

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Genetics in Medicine

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Population-based estimates of ...... primary ovarian insufficiency.

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Claire E Bennett

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Danielle H Morris

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James N Macpherson

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Michael Jones

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Patricia A Jacobs

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Sarah Ennis

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P2860

Clinical practice. Primary ovarian insufficiency

CGG repeat in the FMR1 gene: size matters

Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study--preliminary data

Studies of FRAXA and FRAXE in women with premature ovarian failure.

Intermediate sized CGG repeats are not a common cause of idiopathic premature ovarian failure

Lifetime body size and reproductive factors: comparisons of data recorded prospectively with self reports in middle age.

The FMR1 gene and fragile X-associated tremor/ataxia syndrome.

The Breakthrough Generations Study: design of a long-term UK cohort study to investigate breast cancer aetiology.

Nonlinear association between CGG repeat number and age of menopause in FMR1 premutation carriers.

Reproductive and menstrual history of females with fragile X expansions

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10.1038/GIM.2013.64

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Minouk J Schoemaker

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