Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma sequencing in a case of congenital deafness

Meng Meng; Xuchao Li; Huijuan Ge; Fang Chen; Mingyu Han; Yanyan Zhang; Dongyang Kang; Weiwei Xie; Zhiying Gao; Xiaoyu Pan; Pu Dai; Fanglu Chi; Shengpei Chen; Ping Liu; Chunlei Zhang; Jianjun Cao; Hui Jiang; Xun Xu; Wei Wang; Tao Duan

doi:10.1038/gim.2014.51

Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma sequencing in a case of congenital deafness

Meng Meng, Xuchao Li, Huijuan Ge, Fang Chen, Mingyu Han, Yanyan Zhang, Dongyang Kang, Weiwei Xie, Zhiying Gao, Xiaoyu Pan, Pu Dai, Fanglu Chi, Shengpei Chen, Ping Liu, Chunlei Zhang, Jianjun Cao, Hui Jiang, Xun Xu, Wei Wang, Tao Duan

Biologisk Institut

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

36 Citationer (Scopus)

Originalsprog	Engelsk
Tidsskrift	Genetics In Medicine
Vol/bind	16
Sider (fra-til)	972-976
Antal sider	5
ISSN	1098-3600
DOI	https://doi.org/10.1038/gim.2014.51
Status	Udgivet - 2014

Adgang til dokumentet

10.1038/gim.2014.51

Citationsformater

Meng, M., Li, X., Ge, H., Chen, F., Han, M., Zhang, Y., Kang, D., Xie, W., Gao, Z., Pan, X., Dai, P., Chi, F., Chen, S., Liu, P., Zhang, C., Cao, J., Jiang, H., Xu, X., Wang, W., & Duan, T. (2014). Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma sequencing in a case of congenital deafness. Genetics In Medicine, 16, 972-976. https://doi.org/10.1038/gim.2014.51

Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma sequencing in a case of congenital deafness. / Meng, Meng; Li, Xuchao; Ge, Huijuan; Chen, Fang; Han, Mingyu; Zhang, Yanyan; Kang, Dongyang; Xie, Weiwei; Gao, Zhiying; Pan, Xiaoyu; Dai, Pu; Chi, Fanglu; Chen, Shengpei; Liu, Ping; Zhang, Chunlei; Cao, Jianjun; Jiang, Hui; Xu, Xun; Wang, Wei; Duan, Tao.

I: Genetics In Medicine, Bind 16, 2014, s. 972-976.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

Meng, M, Li, X, Ge, H, Chen, F, Han, M, Zhang, Y, Kang, D, Xie, W, Gao, Z, Pan, X, Dai, P, Chi, F, Chen, S, Liu, P, Zhang, C, Cao, J, Jiang, H, Xu, X, Wang, W & Duan, T 2014, 'Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma sequencing in a case of congenital deafness', Genetics In Medicine, bind 16, s. 972-976. https://doi.org/10.1038/gim.2014.51

Meng, Meng ; Li, Xuchao ; Ge, Huijuan ; Chen, Fang ; Han, Mingyu ; Zhang, Yanyan ; Kang, Dongyang ; Xie, Weiwei ; Gao, Zhiying ; Pan, Xiaoyu ; Dai, Pu ; Chi, Fanglu ; Chen, Shengpei ; Liu, Ping ; Zhang, Chunlei ; Cao, Jianjun ; Jiang, Hui ; Xu, Xun ; Wang, Wei ; Duan, Tao. / Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma sequencing in a case of congenital deafness. I: Genetics In Medicine. 2014 ; Bind 16. s. 972-976.

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title = "Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma sequencing in a case of congenital deafness",

keywords = "deafness, monogenic, noninvasive, plasma, sequencing",

author = "Meng Meng and Xuchao Li and Huijuan Ge and Fang Chen and Mingyu Han and Yanyan Zhang and Dongyang Kang and Weiwei Xie and Zhiying Gao and Xiaoyu Pan and Pu Dai and Fanglu Chi and Shengpei Chen and Ping Liu and Chunlei Zhang and Jianjun Cao and Hui Jiang and Xun Xu and Wei Wang and Tao Duan",

year = "2014",

doi = "10.1038/gim.2014.51",

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volume = "16",

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TY - JOUR

T1 - Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma sequencing in a case of congenital deafness

AU - Meng, Meng

AU - Li, Xuchao

AU - Ge, Huijuan

AU - Chen, Fang

AU - Han, Mingyu

AU - Zhang, Yanyan

AU - Kang, Dongyang

AU - Xie, Weiwei

AU - Gao, Zhiying

AU - Pan, Xiaoyu

AU - Dai, Pu

AU - Chi, Fanglu

AU - Chen, Shengpei

AU - Liu, Ping

AU - Zhang, Chunlei

AU - Cao, Jianjun

AU - Jiang, Hui

AU - Xu, Xun

AU - Wang, Wei

AU - Duan, Tao

PY - 2014

Y1 - 2014

KW - deafness

KW - monogenic

KW - noninvasive

KW - plasma

KW - sequencing

U2 - 10.1038/gim.2014.51

DO - 10.1038/gim.2014.51

M3 - Journal article

C2 - 24830326

VL - 16

SP - 972

EP - 976

JO - Genetics in Medicine

JF - Genetics in Medicine

SN - 1098-3600

ER -