Oligonucleotide microarrays for clinical diagnosis of copy number variation.

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Genome wide analysis of chromosomal alterations in oral squamous cell carcinomas revealed over expression of MGAM and ADAM9.Medical conditions in autism spectrum disorders

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Oligonucleotide microarrays for clinical diagnosis of copy number variation.

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2008 nî lūn-bûn

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2008年の論文

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2008年学术文章

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2008年学术文章

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2008年学术文章

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Oligonucleotide microarrays for clinical diagnosis of copy number variation.

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Oligonucleotide microarrays for clinical diagnosis of copy number variation.

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Item

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Oligonucleotide microarrays for clinical diagnosis of copy number variation.

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Oligonucleotide microarrays for clinical diagnosis of copy number variation.

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Oligonucleotide microarrays for clinical diagnosis of copy number variation.

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Oligonucleotide microarrays for clinical diagnosis of copy number variation.

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P1476

Oligonucleotide microarrays for clinical diagnosis of copy number variation.

@en

P2093

Bai-Lin Wu

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

David T Miller

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Yiping Shen

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P2860

High-resolution genomic microarrays for X-linked mental retardation.

American College of Medical Genetics guideline on the cytogenetic evaluation of the individual with developmental delay or mental retardation.

Oligonucleotide arrays for high-resolution analysis of copy number alteration in mental retardation/multiple congenital anomalies.

Comprehensive validation of array comparative genomic hybridization platforms: how much is enough?

Array comparative genomic hybridization and computational genome annotation in constitutional cytogenetics: suggesting candidate genes for novel submicroscopic chromosomal imbalance syndromes.

Use of array-based technology in the practice of medical genetics.

Practice parameter: evaluation of the child with global developmental delay: report of the Quality Standards Subcommittee of the American Academy of Neurology and The Practice Committee of the Child Neurology Society.

Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more?

Development and validation of a CGH microarray for clinical cytogenetic diagnosis

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Unit 8.12

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scholarly article

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10.1002/0471142905.HG0812S58

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Chapter 8

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P577

2008-07-01T00:00:00Z

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P698

18633976

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Oligonucleotide microarrays for clinical diagnosis of copy number variation.

about

P2860

P2860

Oligonucleotide microarrays for clinical diagnosis of copy number variation.

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type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P577

P698