Reproductive management through integration of PGD and MPS-based noninvasive prenatal screening/diagnosis for a family with GJB2-associated hearing impairment. (Q50351727)

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scientific article published in September 2015

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English	Reproductive management through integration of PGD and MPS-based noninvasive prenatal screening/diagnosis for a family with GJB2-associated hearing impairment.	scientific article published in September 2015

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scholarly article

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Europe PubMed Central

6 March 2018

http://europepmc.org/abstract/MED/26432548

Reproductive management through integration of PGD and MPS-based noninvasive prenatal screening/diagnosis for a family with GJB2-associated hearing impairment. (English)

1 reference

Europe PubMed Central

6 March 2018

http://europepmc.org/abstract/MED/26432548

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based on heuristic

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4 June 2020

author name string

WenPing Xiong

1

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4 June 2020

DaYong Wang

2

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4 June 2020

Yuan Gao

3

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4 June 2020

Ya Gao

4

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4 June 2020

HongYang Wang

5

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4 June 2020

Jing Guan

6

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4 June 2020

Lan Lan

7

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4 June 2020

JunHao Yan

8

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4 June 2020

Liang Zong

9

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4 June 2020

Yuan Yuan

10

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4 June 2020

Wei Dong

11

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4 June 2020

SeXin Huang

12

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KeLiang Wu

13

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4 June 2020

YaoShen Wang

14

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4 June 2020

ZhiLi Wang

15

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4 June 2020

HongMei Peng

16

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4 June 2020

YanPing Lu

17

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4 June 2020

LinYi Xie

18

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4 June 2020

Cui Zhao

19

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4 June 2020

Li Wang

20

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4 June 2020

QiuJing Zhang

21

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4 June 2020

Yun Gao

22

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4 June 2020

Na Li

23

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4 June 2020

Ju Yang

24

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ZiFang Yin

25

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4 June 2020

Bing Han

26

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4 June 2020

Wei Wang

27

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QiuJu Wang

29

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4 June 2020

publication date

1 September 2015

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6 March 2018

http://europepmc.org/abstract/MED/26432548

Science in China. Series C: Life Sciences

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58

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829-838

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4 June 2020

9

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4 June 2020

https://scigraph.springernature.com/pub.10.1007/s11427-015-4936-y

0 references

Newborn hearing screening--a silent revolution

1 reference

https://api.crossref.org/works/10.1007%2FS11427-015-4936-Y

21 January 2018

Procedure-related complications of amniocentesis and chorionic villous sampling: a systematic review

1 reference

https://api.crossref.org/works/10.1007%2FS11427-015-4936-Y

21 January 2018

Procedure-related risk of miscarriage following amniocentesis and chorionic villus sampling: a systematic review and meta-analysis

1 reference

https://api.crossref.org/works/10.1007%2FS11427-015-4936-Y

21 January 2018

[Preimplantaion genetic diagnosis of hearing loss with 35delG mutation in GJB2 gene - preliminary report].

1 reference

https://api.crossref.org/works/10.1007%2FS11427-015-4936-Y

21 January 2018

ESHRE PGD Consortium data collection XII: cycles from January to December 2009 with pregnancy follow-up to October 2010.

1 reference

https://api.crossref.org/works/10.1007%2FS11427-015-4936-Y

21 January 2018

Preimplantation genetic diagnosis (PGD) for nonsyndromic deafness by polar body and blastomere biopsy

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https://api.crossref.org/works/10.1007%2FS11427-015-4936-Y

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS11427-015-4936-Y

21 January 2018

Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China

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https://api.crossref.org/works/10.1007%2FS11427-015-4936-Y

21 January 2018

Clinical utility of noninvasive fetal trisomy (NIFTY) test--early experience.

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21 January 2018

Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies

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21 January 2018

Integration of targeted sequencing and NIPT into clinical practice in a Chinese family with maple syrup urine disease

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21 January 2018

Genetics is a major determinant of expression of the human hepatic uptake transporter OATP1B1, but not of OATP1B3 and OATP2B1

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21 January 2018

Newborn hearing concurrent genetic screening for hearing impairment-a clinical practice in 58,397 neonates in Tianjin, China.

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Blastocyst trophectoderm biopsy and preimplantation genetic diagnosis for familial monogenic disorders and chromosomal translocations.

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21 January 2018

Blastocyst biopsy and vitrification are effective for preimplantation genetic diagnosis of monogenic diseases.

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21 January 2018

The causes of misdiagnosis and adverse outcomes in PGD.

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21 January 2018

Haplotype-based approach for noninvasive prenatal diagnosis of congenital adrenal hyperplasia by maternal plasma DNA sequencing

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21 January 2018

Noninvasive prenatal diagnosis of congenital adrenal hyperplasia using cell-free fetal DNA in maternal plasma

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21 January 2018

Noninvasive prenatal diagnosis of duchenne muscular dystrophy: comprehensive genetic diagnosis in carrier, proband, and fetus

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Technology requirements for preimplantation genetic diagnosis to improve assisted reproduction outcomes.

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World of reproductive biology

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Application of next-generation sequencing technology for comprehensive aneuploidy screening of blastocysts in clinical preimplantation genetic screening cycles

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CGtag: complete genomics toolkit and annotation in a cloud-based Galaxy

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Embryo genome profiling by single-cell sequencing for preimplantation genetic diagnosis in a β-thalassemia family.

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