Hasil Pencarian - Jingfang Zhai

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  1. 1
    Pregnancy outcomes and genetic analysis for fetal ventriculomegaly

    Pregnancy outcomes and genetic analysis for fetal ventriculomegaly oleh Huimin Tao, Huimin Tao, Huimin Tao, Lin Zhang, Fangfang Tan, Fangfang Tan, Yu Han, Yu Han, Yu Han, Xuezhen Wang, Xuezhen Wang, Jiebin Wu, Jiebin Wu, Jingfang Zhai, Jingfang Zhai, Jingfang Zhai

    Diterbitkan 2023-09-01
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  2. 2
    Pathogenic relationship between phenotypes of ARPKD and novel compound heterozygous mutations of PKHD1

    Pathogenic relationship between phenotypes of ARPKD and novel compound heterozygous mutations of PKHD1 oleh Xinrong Zhang, Xinrong Zhang, Xinrong Zhang, Jiebin Wu, Jiebin Wu, Jianteng Zhou, Jie Liang, Jie Liang, Jie Liang, Yu Han, Yu Han, Yu Han, Yunmeng Qi, Yunmeng Qi, Yunmeng Qi, Tao Zhu, Dejian Yuan, Zuobin Zhu, Zuobin Zhu, Jingfang Zhai, Jingfang Zhai, Jingfang Zhai, Jingfang Zhai

    Diterbitkan 2024-07-01
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  3. 3
    Partial trisomy 4q and monosomy 5p inherited from a maternal translocationt(4;5)(q33; p15) in three adverse pregnancies

    Partial trisomy 4q and monosomy 5p inherited from a maternal translocationt(4;5)(q33; p15) in three adverse pregnancies oleh Jingbo Zhang, Bei Zhang, Tong Liu, Huihui Xie, Jingfang Zhai

    Diterbitkan 2020-06-01
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  4. 4
    Genotype-phenotype correlations in a fetus with Kleefstra syndrome

    Genotype-phenotype correlations in a fetus with Kleefstra syndrome oleh Xuezhen Wang, Jiebin Wu, Min Pang, Ying Liu, Jingfang Zhai

    Diterbitkan 2024-03-01
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  5. 5
    An azoospermic male with a novel chromosome 46, XX, der(15)t(Y; 15)(p11.3; p12)

    An azoospermic male with a novel chromosome 46, XX, der(15)t(Y; 15)(p11.3; p12) oleh Jiebin Wu, Guanli Hu, Jingfang Zhai, Conghui Han, Zhenbei Li

    Diterbitkan 2022-07-01
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  6. 6
    Chromosomal abnormalities and Y chromosome microdeletions in infertile men with azoospermia and oligozoospermia in Eastern China

    Chromosomal abnormalities and Y chromosome microdeletions in infertile men with azoospermia and oligozoospermia in Eastern China oleh Jing Sha, Guiping Huang, Bei Zhang, Xia Wang, Zaochun Xu, Jingfang Zhai

    Diterbitkan 2020-10-01
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  7. 7
    Caloric restriction induced epigenetic effects on aging

    Caloric restriction induced epigenetic effects on aging oleh Jingfang Zhai, William H. Kongsberg, Yinbo Pan, Canhua Hao, Xiaojing Wang, Jie Sun

    Diterbitkan 2023-01-01
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  8. 8
    Next-generation Sequencing and Karyotype Analysis for the Diagnosis of Robertsonian Translocation Type Trisomy 13: A Case Report

    Next-generation Sequencing and Karyotype Analysis for the Diagnosis of Robertsonian Translocation Type Trisomy 13: A Case Report oleh Jing SHA, Fumin LIU, Bei ZHANG, Yang HUANG, Qinglin ZHANG, Gao JUAN, Jingfang ZHAI

    Diterbitkan 2017-05-01
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  9. 9
    45, X/ 46, X, psu idic (Y) (q11.2) Mosaicism in a Primary Amenorrhea Girl with Swyer Syndrome

    45, X/ 46, X, psu idic (Y) (q11.2) Mosaicism in a Primary Amenorrhea Girl with Swyer Syndrome oleh Yu Han, Jiebin Wu, Fangfang Tan, Jing Sha, Bei Zhang, Jingfang Zhai, Xuezhen Wang

    Diterbitkan 2023-01-01
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  10. 10
    Efficiency of copy number variation sequencing combined with karyotyping in fetuses with congenital heart disease and the following outcomes

    Efficiency of copy number variation sequencing combined with karyotyping in fetuses with congenital heart disease and the following outcomes oleh Xuezhen Wang, Jing Sha, Yu Han, Min Pang, Min Liu, Mengna Liu, Bei Zhang, Jingfang Zhai

    Diterbitkan 2024-05-01
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  11. 11
    Novel circular RNA circ-0002727 regulates miR-144-3p/KIF14 pathway to promote lung adenocarcinoma progression

    Novel circular RNA circ-0002727 regulates miR-144-3p/KIF14 pathway to promote lung adenocarcinoma progression oleh Yang Li, Xiu Hong, Jingfang Zhai, Ying Liu, Rui Li, Xiuli Wang, Youwei Zhang, Qian Lv

    Diterbitkan 2023-11-01
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  12. 12
    Haploinsufficiencies of FOXF1, FOXC2 and FOXL1 genes originated from deleted 16q24.1q24.2 fragment related with alveolar capillary dysplasia with misalignment of pulmonary veins and lymphedema-distichiasis syndrome: relationship to phenotype

    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... oleh Xuezhen Wang, Lili Guo, Bei Zhang, Jiebin Wu, Yu Sun, Huimin Tao, Jing Sha, Jingfang Zhai, Min Liu

    Diterbitkan 2022-11-01
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  13. 13
    A prenatal case of Simpson-Golabi-Behmel syndrome type 1 with a 0.26-Mb deletion fragment at Xq26.2 inherited from mother

    A prenatal case of Simpson-Golabi-Behmel syndrome type 1 with a 0.26-Mb deletion fragment at Xq26.2 inherited from mother oleh Jing Sha, MD, Fangfang Tan, MD, Ying Liu, BA, Zaochun Xu, BA, Xuezhen Wang, MD, Jingfang Zhai, MD, Maya Saranathan.

    Diterbitkan 2022-04-01
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