KH domain containing 3 like (KHDC3L) frame-shift mutation causes both recurrent pregnancy loss and hydatidiform mole
Author:
Funder
Zanjan University of Medical Sciences
Université Grenoble Alpes
Royan Institute
Publisher
Elsevier BV
Subject
Obstetrics and Gynaecology,Reproductive Medicine
Reference28 articles.
1. Conception to ongoing pregnancy: the “black box” of early pregnancy loss;Macklon;Hum Reprod Update,2002
2. New insights into mechanisms behind miscarriage;Larsen;BMC Med,2013
3. Recurrent pregnancy loss: etiology, diagnosis, and therapy;Ford;Rev Obstet Gynecol,2009
4. Recurrent miscarriage: aetiology, management and prognosis;Li;Hum Reprod Update,2002
5. Terminology for pregnancy loss prior to viability: a consensus statement from the ESHRE early pregnancy special interest group;Kolte;Hum Reprod,2015
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1. Genetics and genomics of recurrent pregnancy loss;Human Reproductive and Prenatal Genetics;2023
2. Understanding recurrent pregnancy loss: recent advances on its etiology, clinical diagnosis, and management;Medical Review;2022-12-01
3. Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith–Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances;Clinical Epigenetics;2022-05-28
4. A familial case of recurrent hydatidiform mole with p.Asp108Ilefs∗30 causing mutation in KHDC3L: A genetic and clinical report;Taiwanese Journal of Obstetrics and Gynecology;2022-03
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