Language
English
German
^M
Dutch
Spanish
Title:
Comparative genomic hybridization using oligonucleotide microarrays and total genomic DNA
Source:
Proceedings of the National Academy of Sciences of the United States of America [0027-8424] Barrett, M T yr:2004
Basic
Full text
Full text available via
PubMed Central
Year:
Volume:
Issue:
Start Page:
Document delivery
Request document via
Library/Bibliothek
Users interested in this article also expressed an interest in the following:
description
1.
Munch, M.
"Detection and subtyping (H5 and H7) of avian type A influenza virus by reverse transcription-PCR and PCR-ELISA."
Archives of virology
146.1 (2001): 87-97.
description
2.
Shaw-Smith, C.
"Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features."
Journal of medical genetics
41.4 (2004): 241-248.
description
3.
Mochel, F.
"Normal intelligence and social interactions in a male patient despite the deletion of NLGN4X and the VCX genes."
European Journal of Medical Genetics
51.1 (2008): 68-73.
description
4.
Ylstra, B..
"BAC to the future! Or oligonucleotides: A perspective for micro array comparative genomic hybridization (array CGH)."
Nucleic Acids Research
34.2 (2006): 445-450.
description
5.
Zahir, F.
"The impact of array genomic hybridization on mental retardation research: a review of current technologies and their clinical utility."
Clinical genetics
72.4 (2007): 271-287.
description
6.
Macarov, M.
"Deletions of VCX-A and NLGN4: A Variable Phenotype Including Normal Intellect."
Journal of intellectual disability research
51.5 (2007): 329-33.
description
7.
Vissers, Lisenka E.
"Array-Based Comparative Genomic Hybridization for the Genomewide Detection of Submicroscopic Chromosomal Abnormalities."
American journal of human genetics
73.6 (2003): 1261-70.
description
8.
Xiao, P. F.
"Combinational synthesis of oligonucleotides and assembly fabrication of oligonucleotide array."
Colloids and surfaces. B, Biointerfaces
40.3 (2005): 165-8.
description
9.
Saberfar, E.
"Multiplex Reverse Transcription-PCR Assay for Detection of Type A Influenza Virus plus Differentiation of Avian H7 and H9 Hemagglutinin Subtypes in Iran."
Iranian journal of public health
38.4 (2009): 29-34.
description
10.
Maeda, M.
"DNA sensors using a ferrocene-oligonucleotide conjugate."
Talanta
56.5 (2002): 857-866.
description
11.
Sala, G.
"ELISA test for the detection of influenza H7 antibodies in avian sera."
Avian Diseases
47.SPEC. ISS. (2003): 1057-1059.
description
12.
Kim, Hye Sung S.
"Altered DNA copy number in patients with different seizure disorder type: by array-CGH."
Brain & development
29.10 (2007): 639-43.
description
13.
Zhao, X.
"An Integrated View of Copy Number and Allelic Alterations in the Cancer Genome Using Single Nucleotide Polymorphism Arrays."
Cancer research
64.9 (2004): 3060-71.
description
14.
de Ravel, T J L J.
"Molecular karyotyping of patients with MCA/MR: the blurred boundary between normal and pathogenic variation."
Cytogenetic and genome research
115.3-4 (2006): 225-30.
description
15.
Ng, L.
"Specific detection of H5N1 avian influenza A virus in field specimens by a one-step RT-PCR assay."
BMC infectious diseases
6.1 (2006): 40-40.
description
16.
Davies, Jonathan J J.
"Array CGH technologies and their applications to cancer genomes."
Chromosome research
13.3 (2005): 237-48.
description
17.
Santacroce, J.
"Measuring parental uncertainty during the diagnosis phase of serious illness in a child."
Journal of pediatric nursing
16.1 (2001): 3-12.
description
18.
Imai, M.
"Rapid diagnosis of H5N1 avian influenza virus infection by newly developed influenza H5 hemagglutinin gene-specific loop-mediated isothermal amplification method."
Journal of Virological Methods
141.2 (2007): 173-180.
description
19.
Khojasteh, M..
"A stepwise framework for the normalization of array CGH data."
BMC bioinformatics
6.1 (2005): 274-274.
description
20.
Remschmidt, H.
"No evidence for involvement of genetic variants in the X-linked neuroligin genes NLGN3 and NLGN4X in probands with autism spectrum disorder on high functioning level."
American journal of medical genetics. Part B, Neuropsychiatric genetics
147B.4 (2007): 535-537.
View More...
View Less...
Select All
Clear All
Save Citations
Select Format
EndNote
Reference Manager
RefWorks
ProCite
Submit citation export
Advanced
Author
Other articles by this author? -- in
GeoRef
author:
Barrett, M T
Scheffer, A
Ben Dor, A
Sampas, N
Lipson, D
Kincaid, R
Tsang, P
Curry, B
Baird, K
Meltzer, P S
Yakhini, Z
Bruhn, L
Laderman, S
last name
initials
Other articles by this author? -- in
Online Contents Geosciences
author:
Barrett, M T
Scheffer, A
Ben Dor, A
Sampas, N
Lipson, D
Kincaid, R
Tsang, P
Curry, B
Baird, K
Meltzer, P S
Yakhini, Z
Bruhn, L
Laderman, S
last name
initials
Other articles by this author? -- using
Web of Science
author:
Barrett, M T
Scheffer, A
Ben Dor, A
Sampas, N
Lipson, D
Kincaid, R
Tsang, P
Curry, B
Baird, K
Meltzer, P S
Yakhini, Z
Bruhn, L
Laderman, S
last name
initials
Web Search
Find related information in
a Web Search Engine
Excite
Google
HotBot
Ixquick
ZOO
Ask
Yahoo!
Bing
Naver
Search Terms:
Search for related information in
Google Scholar
Article Title
Author Name
Journal Title
Other Search
Search Terms:
A service provided by the
Library of the Wissenschaftspark Albert Einstein
, Potsdam, Germany.
© 2005 SFX by Ex Libris Inc.