Clinical utility of array comparative genomic hybridization: uncovering tumor susceptibility in individuals with developmental delay - Wikidata - awgldk - TriplyDB

Clinical utility of array comparative genomic hybridization: uncovering tumor susceptibility in individuals with developmental delay

Clinical utility of array comparative genomic hybridization: uncovering tumor susceptibility in individuals with developmental delay

http://www.wikidata.org/entity/Q33810887

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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 De novo microdeletion of Xp11.3 exclusively encompassing the monoamine oxidase A and B genes in a male infant with episodic hypotonia: a genomics approach to personalized medicine.The clinical impact of chromosomal microarray on paediatric care in Hong Kong.Dosage changes of a segment at 17p13.1 lead to intellectual disability and microcephaly as a result of complex genetic interaction of multiple genes.The clinical context of copy number variation in the human genome.A common molecular mechanism underlies two phenotypically distinct 17p13.1 microdeletion syndromes.Modification of risk for cancer as a coincidental finding in DNA array investigation.Chromosomal microarray impacts clinical management.

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P2860

Clinical utility of array comparative genomic hybridization: uncovering tumor susceptibility in individuals with developmental delay

http://www.wikidata.org/entity/Q33810887

description

2009 nî lūn-bûn

@nan

2009 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի հունվարին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

Clinical utility of array comp ...... duals with developmental delay

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Clinical utility of array comp ...... duals with developmental delay

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Clinical utility of array comp ...... duals with developmental delay

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Clinical utility of array comp ...... duals with developmental delay

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Clinical utility of array comp ...... duals with developmental delay

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Clinical utility of array comp ...... duals with developmental delay

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J.JPEDS.2008.07.045

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The Journal of Pediatrics

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Clinical utility of array comp ...... duals with developmental delay

@en

P2093

Andrea Kwan

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April N Justice

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Louanne Hudgins

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Margaret P Adam

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Susan Schelley

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P2860

A serine/threonine kinase gene defective in Peutz-Jeghers syndrome

Diagnostic genome profiling in mental retardation.

Hamartomatous polyposis syndromes: molecular genetics, neoplastic risk, and surveillance recommendations.

High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.

Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports.

Diagnosing idiopathic learning disability: a cost-effectiveness analysis of microarray technology in the National Health Service of the United Kingdom.

Li-Fraumeni and related syndromes: correlation between tumor type, family structure, and TP53 genotype.

Whole-genome array-CGH identifies novel contiguous gene deletions and duplications associated with developmental delay, mental retardation, and dysmorphic features.

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143-146

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scholarly article

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1

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Christa Lese Martin

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