Journal of Human Reproductive Science
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1What should we consider in the case of combined Down- and 47,XY,+i(X)(q10) Klinefelter syndromes? The unique case of a male newborn and review of the literature
Eva Pinti,Anna Lengyel,Gyorgy Fekete,Iren Haltrich
BMC Pediatrics.2020;20(1)
[DOI]
2Fluorescence in situ hybridisation sperm examination is significantly impaired in all categories of male infertility
S. Petousis,Y. Prapas,A. Papatheodorou,C. Margioula-Siarkou,G. Papatzikas,Y. Panagiotidis,A. Karkanaki,K. Ravanos,N. Prapas
Andrologia.2018;50(2)e12847
[DOI]
3Prevalence and spectrum of chromosome abnormalities among spontaneous and induced early reproductive losses: 2020 miscarriages and 1572 medical abortions
N. P. Veropotvelyan,Y. S. Poguliay,E. S. Savarovskaya
Reproductive Endocrinology.2020;0(55)8
[DOI]
4DOUBLE ANEUPLOIDY: A UNIQUE CASE OF TRISOMY 21 WITH XYY
Abhinav Tiwari,Pranay Trivedi,Wrunda Sakhare,Nohar Singh Thakur,G. Malini Chandramohan
Indian Journal of Child Health.2020;07(04)188
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5Double Aneuploidy Detected by Cell-Free DNA Testing and Confirmed by Fetal Tissue Analysis
Charlene G. Echague,Scott M. Petersen
Obstetrics & Gynecology.2016;127(6)1064
[DOI]
6A multiplex droplet digital PCR assay for non-invasive prenatal testing of fetal aneuploidies
Chianru Tan,Xihua Chen,Fang Wang,Dong Wang,Zongfu Cao,Xiurui Zhu,Chao Lu,Wenjun Yang,Na Gao,Huafang Gao,Yong Guo,Lingxiang Zhu
The Analyst.2019;144(7)2239
[DOI]
7Development of a Chromosomal Microarray Test for the Detection of Abnormalities in Formalin-Fixed, Paraffin-Embedded Products of Conception Specimens
Troy J. Gliem,Umut Aypar
The Journal of Molecular Diagnostics.2017;19(6)843
[DOI]
8Investigation of chromosomal alterations in patients with Alzheimer's disease in the state of Amazonas, Brazil
Kledson Moraes Nunes,Denise Corrêa Benzaquem,Natalia Dayane Moura Carvalho,Talísia Nascimento Vianez,Ernanda Raquel de Queirós Gonçalves de Sousa e Fernandes,Cleiton Fantin
Arquivos de Neuro-Psiquiatria.2019;77(12)855
[DOI]
9Recurrent pregnancy loss evaluation combined with 24-chromosome microarray of miscarriage tissue provides a probable or definite cause of pregnancy loss in over 90% of patients
F Popescu,C R Jaslow,W H Kutteh
Human Reproduction.2018;33(4)579
[DOI]
10Chromosomal abnormalities in products of conception of first-trimester miscarriages detected by conventional cytogenetic analysis: a review of 1000 cases
Larysa Y. Pylyp,Lyudmyla O. Spynenko,Nataliya V. Verhoglyad,Anna O. Mishenko,Dmytro O. Mykytenko,Valery D. Zukin
Journal of Assisted Reproduction and Genetics.2018;35(2)265
[DOI]
11Comparative clinical genetic testing in spontaneous miscarriage: Insights from a study in Southern Chinese women
Meiying Cai,Na Lin,Liangpu Xu,Hailong Huang
Journal of Cellular and Molecular Medicine.2021;25(12)5721
[DOI]
12Follow-up of multiple aneuploidies and single monosomies detected by noninvasive prenatal testing: implications for management and counseling
Holly L. Snyder,Kirsten J. Curnow,Sucheta Bhatt,Diana W. Bianchi
Prenatal Diagnosis.2016;36(3)203
[DOI]
13Karyotype evaluation of repeated abortions in primary and secondary recurrent pregnancy loss
T. V. Nikitina,E. A. Sazhenova,D. I. Zhigalina,E. N. Tolmacheva,N. N. Sukhanova,I. N. Lebedev
Journal of Assisted Reproduction and Genetics.2020;37(3)517
[DOI]
14Clinical utilization of chromosomal microarray analysis for the genetic analysis in subgroups of pregnancy loss
Lingshan Gou,Tianya Liu,Yi Wang,Qin Wu,Shunan Hu,Bulian Dong,Chuanxia Wang,Yan Zhang,Xinghu Shan,Xiaona Wang,Feng Suo,Maosheng Gu
The Journal of Maternal-Fetal & Neonatal Medicine.2020;37(3)1
[DOI]
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