Format
Items per page
Sort by

Send to:

Choose Destination

Links from PubMed

Items: 1 to 20 of 228

1.

Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics.

Cheung SW, Shaw CA, Scott DA, Patel A, Sahoo T, Bacino CA, Pursley A, Li J, Erickson R, Gropman AL, Miller DT, Seashore MR, Summers AM, Stankiewicz P, Chinault AC, Lupski JR, Beaudet AL, Sutton VR.

Am J Med Genet A. 2007 Aug 1;143A(15):1679-86.

PMID:
17607705
2.

Detection of low-level mosaicism by array CGH in routine diagnostic specimens.

Ballif BC, Rorem EA, Sundin K, Lincicum M, Gaskin S, Coppinger J, Kashork CD, Shaffer LG, Bejjani BA.

Am J Med Genet A. 2006 Dec 15;140(24):2757-67.

PMID:
17103431
3.

Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH).

Schoumans J, Ruivenkamp C, Holmberg E, Kyllerman M, Anderlid BM, Nordenskjöld M.

J Med Genet. 2005 Sep;42(9):699-705.

4.

Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more?

Bejjani BA, Saleki R, Ballif BC, Rorem EA, Sundin K, Theisen A, Kashork CD, Shaffer LG.

Am J Med Genet A. 2005 Apr 30;134(3):259-67.

PMID:
15723295
5.

Prenatal diagnosis of mosaic trisomy 8q studied by ultrasound, cytogenetics, and array-CGH.

Wood E, Dowey S, Saul D, Cain C, Rossiter J, Blakemore K, Stetten G.

Am J Med Genet A. 2008 Mar 15;146A(6):764-9. doi: 10.1002/ajmg.a.32184.

PMID:
18241063
6.
7.

Molecular karyotyping: array CGH quality criteria for constitutional genetic diagnosis.

Vermeesch JR, Melotte C, Froyen G, Van Vooren S, Dutta B, Maas N, Vermeulen S, Menten B, Speleman F, De Moor B, Van Hummelen P, Marynen P, Fryns JP, Devriendt K.

J Histochem Cytochem. 2005 Mar;53(3):413-22.

PMID:
15750031
8.

Development and validation of a CGH microarray for clinical cytogenetic diagnosis.

Cheung SW, Shaw CA, Yu W, Li J, Ou Z, Patel A, Yatsenko SA, Cooper ML, Furman P, Stankiewicz P, Lupski JR, Chinault AC, Beaudet AL.

Genet Med. 2005 Jul-Aug;7(6):422-32. Erratum in: Genet Med. 2005 Sep;7(7):478. Stankiewicz, Pawal [corrected to Stankiewicz, Pawel].

PMID:
16024975
9.

Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridization.

del Gaudio D, Yang Y, Boggs BA, Schmitt ES, Lee JA, Sahoo T, Pham HT, Wiszniewska J, Chinault AC, Beaudet AL, Eng CM.

Hum Mutat. 2008 Sep;29(9):1100-7. doi: 10.1002/humu.20841.

PMID:
18752307
10.

Application of a target array comparative genomic hybridization to prenatal diagnosis.

Park JH, Woo JH, Shim SH, Yang SJ, Choi YM, Yang KS, Cha DH.

BMC Med Genet. 2010 Jun 24;11:102. doi: 10.1186/1471-2350-11-102.

11.

[Microarray-based comparative genomic hybridization in the study of constitutional chromosomal abnormalities].

Béri-Dexheimer M, Bonnet C, Chambon P, Brochet K, Grégoire MJ, Jonveaux P.

Pathol Biol (Paris). 2007 Feb;55(1):13-8. Epub 2006 May 11. Review. French.

PMID:
16697120
12.

Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical cases.

Shaffer LG, Kashork CD, Saleki R, Rorem E, Sundin K, Ballif BC, Bejjani BA.

J Pediatr. 2006 Jul;149(1):98-102. Erratum in: J Pediatr. 2006 Oct;149(4):585.

PMID:
16860135
13.

Application of metaphase HR-CGH and targeted Chromosomal Microarray Analyses to genomic characterization of 116 patients with mental retardation and dysmorphic features.

Nowakowska B, Stankiewicz P, Obersztyn E, Ou Z, Li J, Chinault AC, Smyk M, Borg K, Mazurczak T, Cheung SW, Bocian E.

Am J Med Genet A. 2008 Sep 15;146A(18):2361-9. doi: 10.1002/ajmg.a.32475.

PMID:
18698622
14.

[Array-CGH for routine diagnosis of cryptic chromosomal imbalances].

Andrieux J.

Pathol Biol (Paris). 2008 Sep;56(6):368-74. doi: 10.1016/j.patbio.2008.04.011. Epub 2008 Jun 2. Review. French.

PMID:
18514435
15.

Analytical and clinical validity of whole-genome oligonucleotide array comparative genomic hybridization for pediatric patients with mental retardation and developmental delay.

Xiang B, Li A, Valentin D, Nowak NJ, Zhao H, Li P.

Am J Med Genet A. 2008 Aug 1;146A(15):1942-54. doi: 10.1002/ajmg.a.32411.

PMID:
18627053
16.

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.

17.

Prenatal genetic diagnosis using microarray analysis in fetuses with congenital heart defects.

Schmid M, Stary S, Blaicher W, Gollinger M, Husslein P, Streubel B.

Prenat Diagn. 2012 Apr;32(4):376-82. doi: 10.1002/pd.2862. Epub 2011 Oct 24.

PMID:
22025351
18.

Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalance.

Shen Y, Irons M, Miller DT, Cheung SW, Lip V, Sheng X, Tomaszewicz K, Shao H, Fang H, Tang HS, Irons M, Walsh CA, Platt O, Gusella JF, Wu BL.

Clin Chem. 2007 Dec;53(12):2051-9. Epub 2007 Sep 27.

19.

Validation of the Agilent 244K oligonucleotide array-based comparative genomic hybridization platform for clinical cytogenetic diagnosis.

Yu S, Bittel DC, Kibiryeva N, Zwick DL, Cooley LD.

Am J Clin Pathol. 2009 Sep;132(3):349-60. doi: 10.1309/AJCP1BOUTWF6ERYS.

20.

Current status and future prospects of array-based comparative genomic hybridisation.

Snijders AM, Pinkel D, Albertson DG.

Brief Funct Genomic Proteomic. 2003 Apr;2(1):37-45. Review.

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk