About: Familial premature ovarian failure due to an interstitial deletion of the long arm of the X chromosome

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About: Familial premature ovarian failure due to an interstitial deletion of the long arm of the X chromosome Goto Sponge NotDistinct Permalink

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scientific article published on 01 July 1987

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в липні 1987 (uk) article scientifique publié en 1987 (fr) im Juli 1987 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xunetu de 1987 (ast) scientific article published on 01 July 1987 (en)
publication date	wds:Q69078316-D9522D36-1875-4475-91A7-5C5BC845E5B3
publication date	1987-07-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q69078316-51F23023-2DBC-4A2D-9920-FD4CDC66412B wds:Q69078316-598F3C18-A803-43C9-B436-F72C4C30C564 wds:Q69078316-6EE0CFBF-21B2-49FC-B62A-5BF915FA4C80 wds:Q69078316-7A8BA263-4BFF-4272-BF54-B842649FEF78 wds:Q69078316-B771A2B7-F832-49B8-940B-EAB102E09741 wds:Q69078316-F8DDEE04-1E0F-42BF-A4DF-A14108392062
author name string	Atkins L McLaughlin C Page DC Brown LG Turksoy RN Krauss CM
rdfs:label	Familial premature ovarian failure due to an interstitial deletion of the long arm of the X chromosome (en) Familial premature ovarian failure due to an interstitial deletion of the long arm of the X chromosome (nl)
skos:prefLabel	Familial premature ovarian failure due to an interstitial deletion of the long arm of the X chromosome (en) Familial premature ovarian failure due to an interstitial deletion of the long arm of the X chromosome (nl)
name	Familial premature ovarian failure due to an interstitial deletion of the long arm of the X chromosome (en) Familial premature ovarian failure due to an interstitial deletion of the long arm of the X chromosome (nl)
title	wds:Q69078316-A3B71F09-F8D8-4FF7-8199-C407D9262CA0
title	Familial premature ovarian failure due to an interstitial deletion of the long arm of the X chromosome (en)
page(s)	wds:Q69078316-13D1F6B9-61D4-4D94-801B-B4258731F95B
page(s)	125-131
instance of	wds:Q69078316-68CF7055-7881-4C2F-9FF1-2394CFB7FF6E
instance of	scholarly article
main subject	wds:Q69078316-F5FF4FD7-4BFC-481E-820D-E5DE8E803C1D
main subject	premature ovarian failure
PubMed ID	wds:Q69078316-2F8920C8-365C-4FE0-923E-DDFE956BA11A
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/3600701
PubMed ID	3600701
published in	wds:Q69078316-61488C1B-E23F-4198-AF96-59C43EEC9B5F
published in	The New England Journal of Medicine
issue	wds:Q69078316-5651F955-9361-4D8E-9793-C038880313A7
volume	wds:Q69078316-96D929BD-9145-4B4E-96C7-BD43AB5FC0BB
issue	3
volume	317
DOI	wds:Q69078316-0CB7A878-A9EC-45AE-BF56-D8F53318D469
DOI	http://dx.doi.org/10.1056/NEJM198707163170301
DOI	10.1056/NEJM198707163170301
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q69078316
is cites work of	Premature ovarian failure: an update. Ovarian dysgenesis in individuals with chromosomal abnormalities Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1. Premature ovarian failure Genes and premature ovarian failure Premature ovarian failure Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features A cytogenetic and molecular study of a series of 45,X fetuses and their parents The similarity of phenotypic effects caused by Xp and Xq deletions in the human female: a hypothesis Genomic organization and polymorphism of human angiotensin II type 2 receptor: no evidence for its gene mutation in two families of human premature ovarian failure syndrome Detection of submicroscopic deletions in band 17p13 in patients with the Miller-Dieker syndrome. Family history as a predictor of early menopause. Alcohol consumption and age of maternal menopause are associated with menopause onset Mothers and daughters menopausal ages: is there a link? What determines the age at the menopause? Clinical features of young women with hypergonadotropic amenorrhea An association among blepharophimosis, resistant ovary syndrome, and true premature menopause OTEX, an androgen-regulated human member of the paired-like class of homeobox genes Investigating the role of X chromosome breakpoints in premature ovarian failure. Blepharophimosis plus ovarian failure: a likely candidate for a contiguous gene syndrome. Results of cytogenetic investigation in adolescent patients with primary or secondary amenorrhea. Pathogenesis and causes of premature ovarian failure: an update 45,X/46,XX mosaicism in patients with idiopathic premature ovarian failure Choroideremia associated with an X-autosomal translocation X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanation Deletion (X)(q26.1-->q28) in a proband and her mother: molecular characterization and phenotypic-karyotypic deductions A susceptibility gene for premature ovarian failure (POF) maps to proximal Xq28 Premature menopause because of an inherited deletion in the long arm of the X-chromosome Interphase cytogenetics on paraffin-embedded sections of ovary for detection of genomic constitution in a patient with Turner's syndrome and chromosomal mosaicism. Hypoplastic external genitalia in association with X;autosome chromosome translocation. Premature ovarian failure Follicle-stimulating hormone beta gene structure in premature ovarian failure What Is the Best Regimen for Ovarian Stimulation of Poor Responders in ART/IVF? Epigenetic Aberration of FMR1 Gene in Infertile Women with Diminished Ovarian Reserve. Prenatal diagnosis of a familial Xq deletion in a female fetus: a case report The new genetics: molecular technology and reproductive biology. Gene variants identified by whole-exome sequencing in 33 French women with premature ovarian insufficiency
is cites work of	wds:Q41234841-0C56A895-F2AC-4ADE-AA43-A36650ED52BE wds:Q50952223-468F6EEF-CE5D-4697-AEF8-914DDF7980A9 wds:Q67287005-4A85A5F6-EAFF-41CE-815B-9A001275CB1D wds:Q34043887-F4F5CA96-F9AF-46E9-8267-247F14E5648A wds:Q52173427-CCA6376A-4118-4819-BA42-8B0AC1ECDDA3 wds:Q56888493-4656DD16-8DB3-48BD-9587-C907C0C4F16F wds:Q73693897-CA234003-12E4-4F26-ACDC-444293117F5C wds:Q35194344-69E5E271-942E-4082-ADFE-F5B29CD212ED wds:Q34388232-BCD2D34B-753D-4B7F-93AF-AA89EF42AF10 wds:Q40550174-581A1038-41C3-4714-9E4B-73F5C9817C89 wds:Q74770804-CC1054A5-F455-4BE5-B5C8-CCB547A2CE0A wds:Q77919896-9F98DC9D-EE69-464E-BE78-4D418A8F88B0 wds:Q94502602-C2E1E9F3-43A4-45E0-938A-EA71887C7564 wds:Q43164501-55EC9E11-3044-4924-985C-A50990D7A770 wds:Q71808582-25D40CF1-7A34-42AD-94DC-1571A8787DCE

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