Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong - Wikidata - awgldk - TriplyDB

Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong

Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong

http://www.wikidata.org/entity/Q35088343

about

The clinical impact of chromosomal microarray on paediatric care in Hong Kong.Diagnostic yield of array CGH in patients with autism spectrum disorder in Hong Kong A complex intragenic rearrangement of ERCC8 in Chinese siblings with Cockayne syndrome.De Novo San Luis Valley Syndrome-like der(8) Chromosome With a Concomitant dup(8p22) in a Mexican Girl.De novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients.Bridging the gap from prenatal karyotyping to whole-genome array comparative genomic hybridization in Hong Kong: survey on knowledge and acceptance of health-care providers and pregnant women.Triploidy - variability of sonographic phenotypes.

P2860

Q34343633-B308CD55-5A34-4637-B3BA-567FB624515F Q36978639-6A27E80F-BDCD-4142-9774-A3A457F99770 Q37717619-CA700017-1BD0-4411-99D7-FEB8A947F713 Q42369239-FE312416-A172-41CD-91D8-3AE3075B76E6 Q47136130-969EBE0E-B195-4BDE-95B2-B88118360B3A Q48228426-EC946629-CA88-4C9D-877A-5E406F2C6F9F Q48338044-4D69B720-C3A2-4457-A4AF-E198CB572131

P2860

Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong

http://www.wikidata.org/entity/Q35088343

description

2014 nî lūn-bûn

@nan

2014 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong

@ast

Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong

@en

type

label

Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong

@ast

Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong

@en

prefLabel

Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong

@ast

Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong

@en

P1433

Q35088343-A6A0FEEB-8DB4-46C2-A578-B862FB55BA1F

P1476

Q35088343-5E6482FA-7BA5-409B-9DC9-244A8BB8DD4C

P2093

Q35088343-05B12B8E-584B-413B-A582-0513F0E6F67C

Q35088343-19170D50-DA10-40C4-94B2-A2992C85679A

Q35088343-3230E5E5-303C-4EEE-8CC5-C9273BCE2580

Q35088343-369D8619-CABA-43BD-BF7D-845B059CECB3

Q35088343-3C575CEB-13C6-467A-9757-0D8CFBAF3D82

Q35088343-60297A27-6B0C-47EB-AC0A-1546400AEF10

Q35088343-8C51DB58-4602-4A25-8196-3A4E958DD221

Q35088343-A457FD97-377B-4A09-BD56-CB292FAE5561

Q35088343-A9B4E9D0-1897-4EB1-A54E-6AFD7B5AA4C6

Q35088343-CD0EFEAD-0019-4339-8CDD-6BB91B36C4D0

P2860

Q35088343-00998F74-54B9-40BA-AAE6-42F2D2842343

Q35088343-1BB24DC8-17FB-4830-A433-312A0EC2785B

Q35088343-3095F8D3-5004-4AAB-A981-CEA4B16590B4

Q35088343-309DBE67-C146-413D-B3FA-DE90EBA57888

Q35088343-359EB4F3-6C5C-411B-A9F0-BA09B86520FF

Q35088343-3B2D5AA8-9C79-4AE8-8D58-955DDE461DBD

Q35088343-3F170DAD-0217-49D3-83B8-5452452F5B62

Q35088343-458AE108-2794-47D5-9F5F-15FC0ABF69B6

Q35088343-4C1E1BF1-B893-4C33-B747-5FB3832D0E96

Q35088343-50605735-717A-4B19-A78B-4F2B05BE9BB8

P304

Q35088343-58CE2A6E-E40C-46E0-B367-4D2855D97D3A

P31

Q35088343-6041E21E-6B74-4778-B87F-7689E6CFF73D

P356

Q35088343-B4F30230-B6B9-4522-98AC-DE084B03323F

P407

Q35088343-55571952-95D7-4BE0-8827-A690AE3EBAE0

P433

Q35088343-2F10FFD4-2C27-4D44-B6FC-471E278159CA

P478

Q35088343-2985591E-AF7C-4D78-AA8B-48A25875A9B5

P577

Q35088343-133E6E32-94FC-4722-BA00-2B698130F46A

P5875

Q35088343-EF04C87F-4C1E-49A9-B655-CB2A0CA1B4FB

P698

Q35088343-76439A32-97EE-4491-9322-95227352E45F

P921

Q35088343-F4EC13D8-D196-4848-84EC-6B6D095A4C13

P932

Q35088343-EBA8C159-7614-43C5-9272-4D1F1D4BB87E

P356

JOURNAL.PONE.0087988

P1433

P1476

Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong

@en

P2093

Anita S Y Kan

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

Brian H Y Chung

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

C P Lee

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

Elizabeth T Lau

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

K Y Leung

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

Kelvin Y K Chan

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

Mary H Y Tang

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

Pui Wah Hui

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

Sario S Y Chan

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

Simon C K Ding

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

P2860

Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011

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

The inv dup (15) or idic (15) syndrome (Tetrasomy 15q)

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

Chromosome 15q11-13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number.

Integration of microarray technology into prenatal diagnosis: counselling issues generated during the NICHD clinical trial.

The clinical utility of microarray technologies applied to prenatal cytogenetics in the presence of a normal conventional karyotype: a review of the literature.

Chromosomal microarray versus karyotyping for prenatal diagnosis.

Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities

QF-PCR as a stand-alone test for prenatal samples: the first 2 years' experience in the London region.

P304

e87988

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

P31

scholarly article

P356

10.1371/JOURNAL.PONE.0087988

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

P407

P433

2

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

P478

9

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

P577

2014-02-05T00:00:00Z

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

P5875

260127185

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

P698

24505343

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

P921

P932

3914896

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