(Q53664232)

17 May 2018

title

Clinical application of SNP array analysis in first-trimester pregnancy loss: a prospective study. (English)

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17 May 2018

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Y Wang

1

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17 May 2018

Q Cheng

2

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L Meng

3

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C Luo

4

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H Hu

5

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J Zhang

6

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J Cheng

7

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T Xu

8

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T Jiang

9

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D Liang

10

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P Hu

11

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Z Xu

12

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publication date

22 December 2016

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17 May 2018

published in

Clinical Genetics

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17 May 2018

volume

91

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17 May 2018

issue

6

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17 May 2018

page(s)

849-858

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17 May 2018

cites work

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Balanced complex chromosome rearrangements: reproductive aspects. A review.

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Reflex fluorescent in situ hybridization testing for unsuccessful product of conception cultures: a retrospective analysis of 5555 samples attempted by conventional cytogenetics and fluorescent in situ hybridization.

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First-trimester spontaneous pregnancy loss - molecular analysis using multiplex ligation-dependent probe amplification.

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Genomic imbalance in products of conception: single-nucleotide polymorphism chromosomal microarray analysis

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Array-based comparative genomic hybridization is more informative than conventional karyotyping and fluorescence in situ hybridization in the analysis of first-trimester spontaneous abortion

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Informatics enhanced SNP microarray analysis of 30 miscarriage samples compared to routine cytogenetics

21 January 2018

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Diagnostic utility of novel combined arrays for genome-wide simultaneous detection of aneuploidy and uniparental isodisomy in losses of pregnancy

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Diagnostic utility of microarray testing in pregnancy loss.

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Chromosomal copy number analysis on chorionic villus samples from early spontaneous miscarriages by high throughput genetic technology

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Array comparative genomic hybridization for genetic evaluation of fetal loss between 10 and 20 weeks of gestation.

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Tissue sampling technique affects accuracy of karyotype from missed abortions

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1q25.2-q31.3 Deletion in a female with mental retardation, clinodactyly, minor facial anomalies but no growth retardation

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Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis

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Double trisomy in spontaneous miscarriages: cytogenetic and molecular approach.

21 January 2018

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Copy number variations in neurodevelopmental disorders

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Chromosomal microarray versus karyotyping for prenatal diagnosis

21 January 2018

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A population study of chromosome 22q11 deletions in infancy

21 January 2018

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Copy number variants at Williams-Beuren syndrome 7q11.23 region.

21 January 2018

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Prevalence estimation of Williams syndrome

21 January 2018

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Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders.

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Whole exome sequencing in recurrent early pregnancy loss

21 January 2018

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Unexpected fertility and paternal UPD 22.

21 January 2018

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Large cryptic genomic rearrangements with apparently normal karyotypes detected by array-CGH

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U-type exchange is the most frequent mechanism for inverted duplication with terminal deletion rearrangements.

21 January 2018

1 reference

Evaluation and treatment of recurrent pregnancy loss: a committee opinion

21 January 2018

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Spontaneous abortion and recurrent miscarriage: A comparison of cytogenetic diagnosis in 250 cases

21 January 2018

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Cytogenetic diagnosis of "normal 46,XX" karyotypes in spontaneous abortions frequently may be misleading

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/CGE.12926

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17 May 2018

PubMed ID

27883173

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17 May 2018