A fetus of partial urorectal septum malformation sequence characterized by complete septate uterus: A case report

por Zhai, Jingfang, Cao, Shenghan, Wang, Xuezhen, Liu, Ying, Zhang, Bei
Publicado 2023

Genetic analysis and management of a familial hypercholesterolemia pedigree with polygenic variants: Case report

por Han, Yu, Zhang, Lin, Tao, Huimin, Wu, Jiebin, Zhai, Jingfang
Publicado 2023

Partial trisomy 4q and monosomy 5p inherited from a maternal translocationt(4;5)(q33; p15) in three adverse pregnancies

por Zhang, Jingbo, Zhang, Bei, Liu, Tong, Xie, Huihui, Zhai, Jingfang
Publicado 2020

An azoospermic male with a novel chromosome 46, XX, der(15)t(Y; 15)(p11.3; p12)

por Wu, Jiebin, Hu, Guanli, Zhai, Jingfang, Han, Conghui, Li, Zhenbei
Publicado 2022

Alteration of Th17 and Foxp3(+) regulatory T cells in patients with unexplained recurrent spontaneous abortion before and after the therapy of hCG combined with immunoglobulin

por Sha, Jing, Liu, Fumin, Zhai, Jingfang, Liu, Xiaoyun, Zhang, Qinglin, Zhang, Bei
Publicado 2017

Fetus of 8q22.2q24.3 duplication and 13q33.2q34 deletion derived from a maternal balanced translocation

por Liu, Tong, Xie, Huihui, Zhang, Jingbo, Wang, Xia, Sha, Jing, Zhai, Jingfang
Publicado 2020

Chromosomal abnormalities and Y chromosome microdeletions in infertile men with azoospermia and oligozoospermia in Eastern China

por Sha, Jing, Huang, Guiping, Zhang, Bei, Wang, Xia, Xu, Zaochun, Zhai, Jingfang
Publicado 2019

A prenatal case of Simpson-Golabi-Behmel syndrome type 1 with a 0.26-Mb deletion fragment at Xq26.2 inherited from mother: Case report

por Sha, Jing, Tan, Fangfang, Liu, Ying, Xu, Zaochun, Wang, Xuezhen, Zhai, Jingfang
Publicado 2022

Missed diagnosis of lissencephaly after prenatal diagnosis: A case report

por Liu, Mengna, Liu, Xiao, Wu, Jiebin, Sha, Jing, Zhai, Jingfang, Zhang, Bei
Publicado 2023

Caloric restriction induced epigenetic effects on aging

por Zhai, Jingfang, Kongsberg, William H., Pan, Yinbo, Hao, Canhua, Wang, Xiaojing, Sun, Jie
Publicado 2023

45, X/ 46, X, psu idic (Y) (q11.2) Mosaicism in a Primary Amenorrhea Girl with Swyer Syndrome

por Han, Yu, Wu, Jiebin, Tan, Fangfang, Sha, Jing, Zhang, Bei, Zhai, Jingfang, Wang, Xuezhen
Publicado 2023

Pregnancy outcomes and genetic analysis for fetal ventriculomegaly

por Tao, Huimin, Zhang, Lin, Tan, Fangfang, Han, Yu, Wang, Xuezhen, Wu, Jiebin, Zhai, Jingfang
Publicado 2023

Next-generation Sequencing and Karyotype Analysis for the Diagnosis of Robertsonian Translocation Type Trisomy 13: A Case Report

por SHA, Jing, LIU, Fumin, ZHANG, Bei, HUANG, Yang, ZHANG, Qinglin, JUAN, Gao, ZHAI, Jingfang
Publicado 2017

Whole exome sequencing combined with dynamic ultrasound assessments for fetal skeletal dysplasias: 4 case reports

por Wang, Li, Li, Ruiqi, Zhai, Jingfang, Zhang, Bei, Wu, Jiebin, Pang, Libo, Liu, Ying
Publicado 2022

Novel circular RNA circ-0002727 regulates miR-144-3p/KIF14 pathway to promote lung adenocarcinoma progression

por Li, Yang, Hong, Xiu, Zhai, Jingfang, Liu, Ying, Li, Rui, Wang, Xiuli, Zhang, Youwei, Lv, Qian
Publicado 2023

Association Between NLR and NAFLD in Adults Exposed to Famine in Early Life

por Liu, Ying, Zhong, Zhifang, Li, Zhihong, Li, Xin, Zhang, Shengkun, Sun, Jie, Zhai, Jingfang, Liu, Xuekui, Liu, Min
Publicado 2022

A fetus with Bosch-Boonstra-Schaaf optic atrophy syndrome characterized by bilateral ventricle widening: A case report and related literature review

por Sun, Yu, Guo, Lili, Sha, Jing, Tao, Huimin, Wang, Xuezhen, Liu, Ying, Zhai, Jingfang, Wu, Jiebin, Zhao, Yongxiu
Publicado 2022

Haploinsufficiencies of FOXF1, FOXC2 and FOXL1 genes originated from deleted 16q24.1q24.2 fragment related with alveolar capillary dysplasia with misalignment of pulmonary veins an...

por Wang, Xuezhen, Guo, Lili, Zhang, Bei, Wu, Jiebin, Sun, Yu, Tao, Huimin, Sha, Jing, Zhai, Jingfang, Liu, Min
Publicado 2022