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Human molecular cytogenetics: From cells to nucleotides22q11.2 deletions in patients with conotruncal defects: data from 1,610 consecutive casesPrenatal diagnosis of a de novo interstitial deletion of 11q (11q22.3 → q23.3) associated with abnormal ultrasound findings by array comparative genomic hybridization.Do physicians think genomic medicine will be useful for patient care?Women's experiences receiving abnormal prenatal chromosomal microarray testing results.Best diagnostic approach for the genetic evaluation of fetuses after intrauterine death in first, second or third trimester: QF-PCR, karyotyping and/or genome wide SNP array analysis.A prenatal missed diagnosed case of submicroscopic chromosomal abnormalities by karyotyping: the clinical utility of array-based CGH in prenatal diagnostics.The role of high-throughput technologies in clinical cancer genomics.Prevalence, diagnosis and outcome of cleft lip with or without cleft palate in The Netherlands.Detection of fetal chromosomal anomalies: does nuchal translucency measurement have added value in the era of non-invasive prenatal testing?Implementation of high resolution whole genome array CGH in the prenatal clinical setting: advantages, challenges, and review of the literature.Prenatal Diagnosis of Cystic Hygroma related to a Deletion of 16q24.1 with Haploinsufficiency of FOXF1 and FOXC2 Genes.Prevalence, timing of diagnosis and pregnancy outcome of abdominal wall defects after the introduction of a national prenatal screening program.Microdeletions/duplications involving TBX1 gene in fetuses with conotruncal heart defects which are negative for 22q11.2 deletion on fluorescence in-situ hybridization.The introduction of arrays in prenatal diagnosis: a special challenge.Congenital diaphragmatic hernia interval on chromosome 8p23.1 characterized by genetics and protein interaction networks.A convenient qualitative and quantitative method to investigate RHD-RHCE hybrid genes.Supernumerary marker chromosomes derived from chromosome 6: cytogenetic, molecular cytogenetic, and array CGH characterization.
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
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2011年學術文章
@zh-hant
name
From karyotyping to array-CGH in prenatal diagnosis.
@en
From karyotyping to array-CGH in prenatal diagnosis.
@nl
type
label
From karyotyping to array-CGH in prenatal diagnosis.
@en
From karyotyping to array-CGH in prenatal diagnosis.
@nl
prefLabel
From karyotyping to array-CGH in prenatal diagnosis.
@en
From karyotyping to array-CGH in prenatal diagnosis.
@nl
P2093
P2860
P356
P1476
From karyotyping to array-CGH in prenatal diagnosis.
@en
P2093
G H Schuring-Blom
K D Lichtenbelt
N V A M Knoers
P2860
P304
P356
10.1159/000334065
P577
2011-11-12T00:00:00Z