Exploring the cause of early miscarriage with SNP-array analysis and karyotyping.

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Exploring the cause of early miscarriage with SNP-array analysis and karyotyping.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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Exploring the cause of early miscarriage with SNP-array analysis and karyotyping.

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Exploring the cause of early miscarriage with SNP-array analysis and karyotyping.

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Exploring the cause of early miscarriage with SNP-array analysis and karyotyping.

@en

Exploring the cause of early miscarriage with SNP-array analysis and karyotyping.

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Exploring the cause of early miscarriage with SNP-array analysis and karyotyping.

@en

Exploring the cause of early miscarriage with SNP-array analysis and karyotyping.

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P1476

Exploring the cause of early miscarriage with SNP-array analysis and karyotyping.

@en

P2093

Aojie Cai

http://www.w3.org/2001/XMLSchema#string

Li Wang

http://www.w3.org/2001/XMLSchema#string

Nan Bai

http://www.w3.org/2001/XMLSchema#string

Ning Liu

http://www.w3.org/2001/XMLSchema#string

Siying Cui

http://www.w3.org/2001/XMLSchema#string

Suzhen Qu

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Xiangdong Kong

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P2860

Clinical impact of copy number variation analysis using high-resolution microarray technologies: advantages, limitations and concerns

Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities

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

Abnormalities in spontaneous abortions detected by G-banding and chromosomal microarray analysis (CMA) at a national reference laboratory

Reliability of 46,XX results on miscarriage specimens: a review of 1,222 first-trimester miscarriage specimens.

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

New insights into mechanisms behind miscarriage.

Clinical utility of array CGH for the detection of chromosomal imbalances associated with mental retardation and multiple congenital anomalies.

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

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

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1-10

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scholarly article

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10.1080/14767058.2017.1367379

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P577

2017-10-16T00:00:00Z

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P698

29034762

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P921

karyotype

miscarriage