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Hypergonadotropic Ovarian Failure, X-Linked

Known as: X-Linked Hypergonadotropic Ovarian Failure, PREMATURE OVARIAN FAILURE 1, Fragile X Associated Primary Ovarian Insufficiency 
National Institutes of Health

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3 relations

Broader (1)

Ovarian Failure, Premature
POF1B genePremature Menopause

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Author response for "Novel phenotype of syndromic premature ovarian insufficiency associated with TP63 molecular defect"
2019
2019
Variation analysis of tousled like kinase 1 gene in patients with sporadic premature ovarian insufficiency
Abstract Tousled like kinase 1 (TLK1), a member of DNA repair family, participates in the regulation of chromatin assembly and is… 
2015
2015
Molecular cloning and mRNA expression analysis of antizyme inhibitor 1 in the ovarian follicles of the Sichuan white goose.
2013
2013
Centers for Collaborative Research in Fragile X (U01): RFA-HD-13-004
Components of Participating Organizations Eunice Kennedy Shriver National Institute of Child Health and Human Development… 
2010
2010
Novel single-nucleotide polymorphisms of LHX8 gene in Korean women with premature ovarian insufficiency
LHX8 (LIM homeobox 8) is a germ cell-specific transcription factor that is crucial for folliculogenesis in the ovary and… 
2010
2010
A faster strategy for prenatal diagnosis of fragile X syndrome
Fragile X syndrome (FXS; OMIM # 309 550), an Xlinked dominant disorder with reduced penetrance, is the most common form of… 
2010
2010
Premature ovarian failure, absence of pubic and axillary hair with de novo 46,X,t(X;15)(q24;q26.3)
We report on an adolescent girl with premature ovarian failure (POF), de novo unbalanced translocation X;15(q24;q26.3) with… 
2010
2010
Premature Ovarian Failure , Absence of Pubic and Axillary Hair With De Novo 46 , X , t ( X ; 15 ) ( q 24 ; q 26 . 3 )
Premature Ovarian Failure, Absence of Pubic and Axillary Hair With De Novo 46,X,t(X;15)(q24;q26.3) Claudio Giacomozzi, Francesca… 
2008
2008
Genetik des Premature Ovarian Failure Syndroms (POF): X-chromosomale Genexpression in POF1, 2, 3 – Molekulargenetische POF–Kausal-Diagnostik
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