Traditional karyotyping vs copy number variation sequencing for detection of chromosomal abnormalities associated with spontaneous miscarriage.

Traditional karyotyping vs copy number variation sequencing for detection of chromosomal abnormalities associated with spontaneous miscarriage.

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http://www.wikidata.org/entity/Q41231906
Cytogenetic analysis of spontaneously discharged products of conception by array-based comparative genomic hybridization.Characterization of chromosomal abnormalities in pregnancy losses reveals critical genes and loci for human early development.Low-pass whole-genome sequencing in clinical cytogenetics: a validated approach.Copy-Number Variants Detection by Low-Pass Whole-Genome Sequencing.Novel rapid molecular diagnosis of fetal chromosomal abnormalities associated with recurrent pregnancy loss.Copy number variation sequencing-based prenatal diagnosis using cell-free fetal DNA in amniotic fluid.Identification of copy number variations associated with congenital heart disease by chromosomal microarray analysis and next-generation sequencingDeletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy
P2860

Traditional karyotyping vs copy number variation sequencing for detection of chromosomal abnormalities associated with spontaneous miscarriage.

Item
http://www.wikidata.org/entity/Q41231906
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Traditional karyotyping vs cop ...... with spontaneous miscarriage.
@en
type
label
Traditional karyotyping vs cop ...... with spontaneous miscarriage.
@en
prefLabel
Traditional karyotyping vs cop ...... with spontaneous miscarriage.
@en
P1433
P1476
P2093
P2860
P304
P31
P356
P433
P478
P577
P698
P921
P356
P1433
P1476
Traditional karyotyping vs cop ...... with spontaneous miscarriage.
@en
P2093
P2860
P304
P31
P356
P433
P478
P577
P698
P921