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Results: 11

1.

Genome-wide copy number analysis in pediatric glioblastoma multiforme.

Giunti L, Pantaleo M, Sardi I, Provenzano A, Magi A, Cardellicchio S, Castiglione F, Tattini L, Novara F, Buccoliero AM, de Martino M, Genitori L, Zuffardi O, Giglio S.

Am J Cancer Res. 2014 May 26;4(3):293-303. eCollection 2014.

PMID:
24959384
[PubMed]
Free PMC Article
2.

Computational methods for detecting copy number variations in cancer genome using next generation sequencing: principles and challenges.

Liu B, Morrison CD, Johnson CS, Trump DL, Qin M, Conroy JC, Wang J, Liu S.

Oncotarget. 2013 Nov;4(11):1868-81.

PMID:
24240121
[PubMed - in process]
Free PMC Article
3.

Progenetix: 12 years of oncogenomic data curation.

Cai H, Kumar N, Ai N, Gupta S, Rath P, Baudis M.

Nucleic Acids Res. 2014 Jan;42(Database issue):D1055-62. doi: 10.1093/nar/gkt1108. Epub 2013 Nov 12.

PMID:
24225322
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Simple, rapid and inexpensive quantitative fluorescent PCR method for detection of microdeletion and microduplication syndromes.

Stofanko M, Gon├žalves-Dornelas H, Cunha PS, Pena HB, Vianna-Morgante AM, Pena SD.

PLoS One. 2013 Apr 19;8(4):e61328. doi: 10.1371/journal.pone.0061328. Print 2013.

PMID:
23620743
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Segmental Maternal UPD6 with Prenatal Growth Restriction.

Poke G, Doody M, Prado J, Gattas M.

Mol Syndromol. 2013 Jan;3(6):270-3. doi: 10.1159/000345168. Epub 2012 Nov 20.

PMID:
23599697
[PubMed]
Free PMC Article
6.

The utility of chromosomal microarray analysis in developmental and behavioral pediatrics.

Beaudet AL.

Child Dev. 2013 Jan-Feb;84(1):121-32. doi: 10.1111/cdev.12050. Epub 2013 Jan 11.

PMID:
23311723
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Clinical impact of copy number variation analysis using high-resolution microarray technologies: advantages, limitations and concerns.

Coughlin CR 2nd, Scharer GH, Shaikh TH.

Genome Med. 2012 Oct 30;4(10):80. doi: 10.1186/gm381. eCollection 2012. Review.

PMID:
23114084
[PubMed]
Free PMC Article
8.

Physicians' perspectives on the uncertainties and implications of chromosomal microarray testing of children and families.

Reiff M, Ross K, Mulchandani S, Propert KJ, Pyeritz RE, Spinner NB, Bernhardt BA.

Clin Genet. 2013 Jan;83(1):23-30. doi: 10.1111/cge.12004. Epub 2012 Sep 18.

PMID:
22989118
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

What have we learnt about the causes of ADHD?

Thapar A, Cooper M, Eyre O, Langley K.

J Child Psychol Psychiatry. 2013 Jan;54(1):3-16. doi: 10.1111/j.1469-7610.2012.02611.x. Epub 2012 Sep 11. Review.

PMID:
22963644
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

The impact of genomics on pediatric research and medicine.

Connolly JJ, Hakonarson H.

Pediatrics. 2012 Jun;129(6):1150-60. doi: 10.1542/peds.2011-3636. Epub 2012 May 7. Review.

PMID:
22566424
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Heterogeneous lengths of copy number mutations in human coagulopathy revealed by genome-wide high-density SNP array.

Kim HJ, Kim DK, Yoo KY, You CW, Yoo JH, Lee KO, Park IA, Choung HS, Kim HJ, Song MJ, Kim SH.

Haematologica. 2012 Feb;97(2):304-9. doi: 10.3324/haematol.2011.052324. Epub 2011 Oct 11.

PMID:
21993689
[PubMed - indexed for MEDLINE]
Free PMC Article

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