Array-based comparative genomic hybridization: clinical contexts for targeted and whole-genome designs. - Wikidata - wikimedia - TriplyDB

Array-based comparative genomic hybridization: clinical contexts for targeted and whole-genome designs.

Array-based comparative genomic hybridization: clinical contexts for targeted and whole-genome designs.

http://www.wikidata.org/entity/Q36943622

about

Genomics in mammalian cell culture bioprocessing Species and gene divergence in Littorina snails detected by array comparative genomic hybridization Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies Genome-wide oligonucleotide array comparative genomic hybridization for etiological diagnosis of mental retardation: a multicenter experience of 1499 clinical cases.Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardation.Bacterial artificial chromosome-emulation oligonucleotide arrays for targeted clinical array-comparative genomic hybridization analyses.Genomic imbalances in neonates with birth defects: high detection rates by using chromosomal microarray analysis.Clinical laboratory implementation of cytogenomic microarrays.Is gene discovery research or diagnosis?Genetic testing practices in infants with congenital heart disease.The clinical utility of molecular karyotyping using high-resolution array-comparative genomic hybridization.Microdeletion Syndromes

P2860

Q27004367-86E65738-82C7-4031-B496-79EDD345F101 Q28656352-3491058F-8A4B-41A3-AC73-40D542DB7AE7 Q28752220-CE910D90-A08D-448E-B639-9E04BB9C675E Q33856221-4C547E87-9ECE-4FAB-A5DD-D6FB64B40225 Q33856401-CD3F7790-43D1-4C6D-942D-4773B02BA2EE Q37435423-BE148762-8AA0-45EB-BD71-D57C0FD57B1E Q37482343-7E1C49EE-B51F-4E02-B47F-B5A18AFA5F1D Q37936089-D3B502BB-8A9E-4AE3-B86A-42CDACA63DA4 Q38442473-02621E89-B0BB-4218-8422-423CE337024B Q46505593-D77541A9-3A90-40A5-9447-C3A36479DCA4 Q50306612-27AB3ACE-DE93-4E93-B67B-9E27410D0C58 Q56535874-B8517016-FF8A-4605-A427-7EBE74A34283

P2860

Array-based comparative genomic hybridization: clinical contexts for targeted and whole-genome designs.

http://www.wikidata.org/entity/Q36943622

description

2007 nî lūn-bûn

@nan

2007年の論文

@ja

2007年論文

@yue

2007年論文

@zh-hant

2007年論文

@zh-hk

2007年論文

@zh-mo

2007年論文

@zh-tw

2007年论文

@wuu

2007年论文

@zh

2007年论文

@zh-cn

name

Array-based comparative genomi ...... eted and whole-genome designs.

@en

type

label

Array-based comparative genomi ...... eted and whole-genome designs.

@en

prefLabel

Array-based comparative genomi ...... eted and whole-genome designs.

@en

P1433

Q36943622-39B278C7-6FD1-41C8-8588-2CEB1E380249

P1476

Q36943622-3ECF2C6D-0FD6-4D5C-8165-807CEFCE9F7B

P2093

Q36943622-1E03C1AE-0346-4D2A-A292-9E29482623B8

Q36943622-DAC777A5-959F-4CA9-91DA-E12D7B5A8C21

P2860

Q36943622-02C2E594-4D1D-4596-901F-E8646BF01B89

Q36943622-059D4D91-944C-42E1-9AB6-3A1B30A54314

Q36943622-0D233817-135D-46E5-9A48-7C23B2E013B0

Q36943622-0E0CEA17-3AF5-4BFE-A985-2EE7558DD0AD

Q36943622-0E749B22-756C-4ACD-969E-0A63C7314AD9

Q36943622-13D1A31D-168F-44FB-A76C-21E403271567

Q36943622-1589FA35-399F-4DBA-A9EA-AE4C559C2CF2

Q36943622-1F3F8608-8FCF-4220-BEDB-2509F93060B3

Q36943622-2974CB07-DDDA-424C-A6B7-C50073B740AE

Q36943622-2F03E8EE-D979-46A8-AD32-780139FE8642

P2888

Q36943622-1E382C53-2E0D-4440-B247-E91D814435BB

P304

Q36943622-CADD624C-7704-40F5-B483-D1C557BCD901

P31

Q36943622-0C39A1A3-CABB-48EB-B16F-1981CA08139E

P356

Q36943622-3DDF8D2B-A03D-444A-89A8-486E2E381817

P407

Q36943622-0EEA4A30-1B8D-4DD9-9EA6-33BDBF8F548C

P433

Q36943622-2B5D300B-FCD6-4AA5-A080-D610AD187F73

P478

Q36943622-96FB601D-FB83-4FC9-B6ED-9C1741B03442

P577

Q36943622-A345127F-A1C4-40DC-B287-7C35E7C8E1E3

P6179

Q36943622-C3DB5276-961D-43EB-96DF-65E8B420C2C3

P698

Q36943622-17D0C957-8930-4BE1-A5FC-CDEEB70E7801

P356

GIM.0B013E318149E354

P1433

Genetics in Medicine

P1476

Array-based comparative genomi ...... eted and whole-genome designs.

@en

P2093

Athena M Cherry

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

Swaroop Aradhya

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

P2860

Structural variation in the human genome

Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking duplicons

Global variation in copy number in the human genome

Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features

Detection of large-scale variation in the human genome

Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability

Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome.

Exon array CGH: detection of copy-number changes at the resolution of individual exons in the human genome.

Copy number variation: new insights in genome diversity.

Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome.

P2888

gim.0b013e318149e354

P304

553-559

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

P31

scholarly article

P356

10.1097/GIM.0B013E318149E354

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

P407

P433

9

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

P478

9

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

P577

2007-09-01T00:00:00Z

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

P6179

1030575757

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

P698

17873642

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