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Items: 1 to 20 of 228

1.

Detection of small genomic imbalances using microarray-based multiplex amplifiable probe hybridization.

Patsalis PC, Kousoulidou L, Männik K, Sismani C, Zilina O, Parkel S, Puusepp H, Tõnisson N, Palta P, Remm M, Kurg A.

Eur J Hum Genet. 2007 Feb;15(2):162-72. Epub 2006 Nov 22.

2.

MAPH: from gels to microarrays.

Patsalis PC, Kousoulidou L, Sismani C, Männik K, Kurg A.

Eur J Med Genet. 2005 Jul-Sep;48(3):241-9. Review.

PMID:
16179220
3.

Array-MAPH: a methodology for the detection of locus copy-number changes in complex genomes.

Kousoulidou L, Männik K, Sismani C, Zilina O, Parkel S, Puusepp H, Tõnisson N, Palta P, Remm M, Kurg A, Patsalis PC.

Nat Protoc. 2008;3(5):849-65. doi: 10.1038/nprot.2008.49.

PMID:
18451793
4.

Multiplex Amplifiable Probe Hybridization (MAPH) methodology as an alternative to comparative genomic hybridization (CGH).

Kousoulidou L, Sismani C, Patsalis PC.

Methods Mol Biol. 2010;653:47-71. doi: 10.1007/978-1-60761-759-4_4. Review.

PMID:
20721737
5.

Screening of 20 patients with X-linked mental retardation using chromosome X-specific array-MAPH.

Kousoulidou L, Parkel S, Zilina O, Palta P, Puusepp H, Remm M, Turner G, Boyle J, van Bokhoven H, de Brouwer A, Van Esch H, Froyen G, Ropers HH, Chelly J, Moraine C, Gecz J, Kurg A, Patsalis PC.

Eur J Med Genet. 2007 Nov-Dec;50(6):399-410. Epub 2007 Sep 29.

PMID:
17980689
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8.

[A novel oligonucleotide arrays-based multiplex amplifiable probe hybridization technology].

Liu HP, Wang H, Lu ZH, Liu XP, Xia K, Xia JH.

Yi Chuan Xue Bao. 2004 Feb;31(2):119-24. Chinese.

PMID:
15473300
9.

X chromosome array-CGH for the identification of novel X-linked mental retardation genes.

Bauters M, Van Esch H, Marynen P, Froyen G.

Eur J Med Genet. 2005 Jul-Sep;48(3):263-75.

PMID:
16179222
10.
11.

Validation of a targeted DNA microarray for the clinical evaluation of recurrent abnormalities in chronic lymphocytic leukemia.

Patel A, Kang SH, Lennon PA, Li YF, Rao PN, Abruzzo L, Shaw C, Chinault AC, Cheung SW.

Am J Hematol. 2008 Jul;83(7):540-6.

12.

Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations.

Le Caignec C, Boceno M, Saugier-Veber P, Jacquemont S, Joubert M, David A, Frebourg T, Rival JM.

J Med Genet. 2005 Feb;42(2):121-8.

13.

Comprehensive detection of genomic duplications and deletions in the DMD gene, by use of multiplex amplifiable probe hybridization.

White S, Kalf M, Liu Q, Villerius M, Engelsma D, Kriek M, Vollebregt E, Bakker B, van Ommen GJ, Breuning MH, den Dunnen JT.

Am J Hum Genet. 2002 Aug;71(2):365-74. Epub 2002 Jul 8.

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Microarray-based comparative genomic hybridization and its applications in human genetics.

Oostlander AE, Meijer GA, Ylstra B.

Clin Genet. 2004 Dec;66(6):488-95. Review.

PMID:
15521975
17.

Diagnostic utility of array-based comparative genomic hybridization in a clinical setting.

Baris HN, Tan WH, Kimonis VE, Irons MB.

Am J Med Genet A. 2007 Nov 1;143A(21):2523-33.

PMID:
17910064
18.

Detection of copy number changes at the NF1 locus with improved high-resolution array CGH.

Shen MH, Mantripragada K, Dumanski JP, Frayling I, Upadhyaya M.

Clin Genet. 2007 Sep;72(3):238-44.

PMID:
17718862
19.

Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.

Kloth JN, Oosting J, van Wezel T, Szuhai K, Knijnenburg J, Gorter A, Kenter GG, Fleuren GJ, Jordanova ES.

BMC Genomics. 2007 Feb 20;8:53.

20.

Detection of exonic copy-number changes using a highly efficient oligonucleotide-based comparative genomic hybridization-array method.

Saillour Y, Cossée M, Leturcq F, Vasson A, Beugnet C, Poirier K, Commere V, Sublemontier S, Viel M, Letourneur F, Barbot JC, Deburgrave N, Chelly J, Bienvenu T.

Hum Mutat. 2008 Sep;29(9):1083-90. doi: 10.1002/humu.20829.

PMID:
18683213

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