相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。A genomics approach to females with infertility and recurrent pregnancy loss
Sateesh Maddirevula et al.
HUMAN GENETICS (2020)
Definitions of infertility and recurrent pregnancy loss: a committee opinion
FERTILITY AND STERILITY (2020)
Inherited thrombophilia and pregnancy loss. Study of an Argentinian cohort
Silvia Peres Wingeyer et al.
MEDICINA CLINICA (2019)
Genetic Variants Contributing to Early Recurrent Pregnancy Loss Etiology Identified by Sequencing Approaches
Paula Quintero-Ronderos et al.
Reproductive Sciences (2019)
Obstetrical and postpartum complications in women with hereditary fibrinogen disorders: A systematic literature review
Vivian Valiton et al.
HAEMOPHILIA (2019)
Genetic diagnosis in first or second trimester pregnancy loss using exome sequencing: a systematic review of human essential genes
Sarah M. Robbins et al.
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS (2019)
Risk of bleeding and thrombosis in inherited qualitative fibrinogen disorders
Giancarlo Castaman et al.
EUROPEAN JOURNAL OF HAEMATOLOGY (2019)
Exome sequencing identifies variants in FKBP4 that are associated with recurrent fetal loss in humans
Charalambos Demetriou et al.
HUMAN MOLECULAR GENETICS (2019)
FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsia
Paula Quintero-Ronderos et al.
MOLECULAR MEDICINE (2019)
CAPS Mutations Are Potentially Associated with Unexplained Recurrent Pregnancy Loss
Hong Pan et al.
AMERICAN JOURNAL OF PATHOLOGY (2019)
KHDC3L mutation causes recurrent pregnancy loss by inducing genomic instability of human early embryonic cells
Weidao Zhang et al.
PLOS BIOLOGY (2019)
NLRP7 and KHDC3L variants in Chinese patients with recurrent hydatidiform moles
Mingliang Ji et al.
JAPANESE JOURNAL OF CLINICAL ONCOLOGY (2019)
Biallelic PADI6 variants linking infertility, miscarriages, and hydatidiform moles
JianHua Qian et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2018)
Genetic and epigenetic variations associated with idiopathic recurrent pregnancy loss
Luis Alejandro Arias-Sosa et al.
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS (2018)
The genetics of recurrent hydatidiform moles: new insights and lessons from a comprehensive analysis of 113 patients
Ngoc Minh Phuong Nguyen et al.
MODERN PATHOLOGY (2018)
Analysis of C3 Gene Variants in Patients With Idiopathic Recurrent Spontaneous Pregnancy Loss
Frida C. Mohlin et al.
FRONTIERS IN IMMUNOLOGY (2018)
Association of the F13A1 Val34Leu polymorphism and recurrent pregnancy loss: A meta-analysis
Jae Hyun Jung et al.
EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY (2017)
Systematic review and meta-analysis of genetic association studies in idiopathic recurrent spontaneous abortion
Nina Pereza et al.
FERTILITY AND STERILITY (2017)
Forkhead box a2 (FOXA2) is essential for uterine function and fertility
Andrew M. Kelleher et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2017)
THBD sequence variants potentially related to recurrent pregnancy loss
Paula Quintero-Ronderos et al.
REPRODUCTIVE BIOLOGY AND ENDOCRINOLOGY (2017)
Novel genes and mutations in patients affected by recurrent pregnancy loss
Paula Quintero-Ronderos et al.
PLOS ONE (2017)
Recurrent pregnancy loss: current perspectives
Hady El Hachem et al.
INTERNATIONAL JOURNAL OF WOMENS HEALTH (2017)
Identification of a Novel Nonsense Mutation in the FOXP3 Gene in a Fetus with Hydrops-Expanding the Phenotype of IPEX Syndrome
Sara L. Reichert et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2016)
Association between maternal, fetal and paternal MTHFR gene C677T and A1298C polymorphisms and risk of recurrent pregnancy loss: a comprehensive evaluation
Yi Yang et al.
ARCHIVES OF GYNECOLOGY AND OBSTETRICS (2016)
Methylenetetrahydrofolate reductase gene polymorphisms and recurrent pregnancy loss in China: a systematic review and meta-analysis
Hui Chen et al.
ARCHIVES OF GYNECOLOGY AND OBSTETRICS (2016)
Blood coagulation factor XIII and factor XIII deficiency
Akbar Dorgalaleh et al.
BLOOD REVIEWS (2016)
Genetic Causes of Recurrent Pregnancy Loss
JESSICA M. PAGE et al.
CLINICAL OBSTETRICS AND GYNECOLOGY (2016)
Coagulation Factor XIIIA Subunit Missense Mutations Affect Structure and Function at the Various Steps of Factor XIII Action
Anne Thomas et al.
HUMAN MUTATION (2016)
Whole exome sequencing in recurrent early pregnancy loss
Ying Qiao et al.
MOLECULAR HUMAN REPRODUCTION (2016)
Congenital afibrinogenemia: Identification and characterization of two novel homozygous fibrinogen Aα and Bβ chain mutations in two Tunisian families
Yessine Amri et al.
THROMBOSIS RESEARCH (2016)
Novel missensemutation in WNT6 in 100 couples with unexplained recurrent miscarriage
Yimei Zhang et al.
HUMAN REPRODUCTION (2015)
Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management
A. Casini et al.
JOURNAL OF THROMBOSIS AND HAEMOSTASIS (2015)
Factor V Leiden mutation in women with early recurrent pregnancy loss: a meta-analysis and systematic review of the causal association
C. Sergi et al.
ARCHIVES OF GYNECOLOGY AND OBSTETRICS (2015)
Eight novel F13A1 gene missense mutations in patients with mild FXIII deficiency: in silico analysis suggests changes in FXIII-A subunit structure/function
Arijit Biswas et al.
ANNALS OF HEMATOLOGY (2014)
Expression and regulation of Foxa2 in the rat uterus during early pregnancy
Kazuki Yamagami et al.
JOURNAL OF REPRODUCTION AND DEVELOPMENT (2014)
Unexplained Recurrent Pregnancy Loss
Sotirios H. Saravelos et al.
OBSTETRICS AND GYNECOLOGY CLINICS OF NORTH AMERICA (2014)
Analysis of genes coding for CD46, CD55, and C4b-binding protein in patients with idiopathic, recurrent, spontaneous pregnancy loss
Frida C. Mohlin et al.
EUROPEAN JOURNAL OF IMMUNOLOGY (2013)
Lifting the lid on unborn lethal Mendelian phenotypes through exome sequencing
Hanan E. Shamseldin et al.
GENETICS IN MEDICINE (2013)
Congenital Fibrinogen Disorders: An Update
Philippe de Moerloose et al.
SEMINARS IN THROMBOSIS AND HEMOSTASIS (2013)
Evaluation and treatment of recurrent pregnancy loss: a committee opinion
FERTILITY AND STERILITY (2012)
A genome-wide scan in affected sibling pairs with idiopathic recurrent miscarriage suggests genetic linkage
A. M. Kolte et al.
MOLECULAR HUMAN REPRODUCTION (2011)
Management of pregnancy and delivery in women with inherited bleeding disorders
Flora Peyvandi et al.
SEMINARS IN FETAL & NEONATAL MEDICINE (2011)
Foxa2 Is Essential for Mouse Endometrial Gland Development and Fertility
Jae-Wook Jeong et al.
BIOLOGY OF REPRODUCTION (2010)
Stimulation of Chemokine and Cytokine Secretion from Cultured Human Primary Decidual Cells: Role of Bacterial Cell Wall Products and TNF alpha
Wei Li et al.
REPRODUCTIVE SCIENCES (2010)
Genome-Wide Screening for Risk Loci of Idiopathic Recurrent Miscarriage in a Han Chinese Population: A Pilot Study
Li Wang et al.
REPRODUCTIVE SCIENCES (2010)
A novel frameshift mutation in FGA accounting for congenital afibrinogenemia predicted to encode an aberrant peptide terminating 158 amino acids downstream
H. Robert-Ebadi et al.
BLOOD COAGULATION & FIBRINOLYSIS (2009)
Factor XIII Deficiency
Mehran Karimi et al.
SEMINARS IN THROMBOSIS AND HEMOSTASIS (2009)
Maternal fibrinogen is necessary for embryonic development
T Iwaki et al.
CURRENT DRUG TARGETS (2005)
Coagulation factor deficiencies and pregnancy loss
A Inbal et al.
SEMINARS IN THROMBOSIS AND HEMOSTASIS (2003)
分享论文
