(Q36875307)

English

Identification of PKD2 mutations in human preimplantation embryos in vitro using a combination of targeted next-generation sequencing and targeted haplotyping

scientific article published on 6 May 2016

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Identification of PKD2 mutations in human preimplantation embryos in vitro using a combination of targeted next-generation sequencing and targeted haplotyping (English)

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

author name string

Song-Chang Chen

1

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Xiao-Li Xu

2

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Jun-Yu Zhang

3

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Guo-Lian Ding

4

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Li Jin

5

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Bei Liu

6

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Dong-Mei Sun

7

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Chang-Lin Mei

8

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Xiao-Nan Yang

9

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

He-Feng Huang

10

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Chen-Ming Xu

11

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

language of work or name

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publication date

6 May 2016

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Europe PubMed Central

PMC publication ID

16 August 2017

Scientific Reports

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Europe PubMed Central

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16 August 2017

6

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

25488

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

copyright license

Creative Commons Attribution 4.0 International

1 May 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

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https://scigraph.springernature.com/pub.10.1038/srep25488

0 references

Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4858692

29 September 2017

Preimplantation genetic diagnosis guided by single-cell genomics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4858692

29 September 2017

Next generation sequencing (NGS) strategies for the genetic testing of myopathies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4858692

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4858692

29 September 2017

Identification of sequence variants in genetic disease-causing genes using targeted next-generation sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4858692

29 September 2017

The next-generation sequencing technology and application

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4858692

29 September 2017

Whole genome amplification in preimplantation genetic diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4858692

29 September 2017

The International HapMap Project

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4858692

29 September 2017

Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4858692

29 September 2017

Recent advances in preimplantation genetic diagnosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4858692

4 September 2018

Combination of multiple displacement amplification with short tandem repeat polymorphismin preimplantation genetic diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4858692

4 September 2018

A short-read multiplex sequencing method for reliable, cost-effective and high-throughput genotyping in large-scale studies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4858692

4 September 2018

Multiple displacement amplification on single cell and possible PGD applications.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4858692

4 September 2018

Karyomapping: a universal method for genome wide analysis of genetic disease based on mapping crossovers between parental haplotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/27150309

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Analysis and application of SNP and haplotype in the human genome]

1 reference

https://pubmed.ncbi.nlm.nih.gov/27150309

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/SREP25488

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

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0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

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