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1.

Oligoarray comparative genomic hybridization-mediated mapping of suppressor mutations generated in a deletion-biased mutagenesis screen.

Jones MR, Rose AM, Baillie DL.

G3 (Bethesda). 2012 Jun;2(6):657-63. doi: 10.1534/g3.112.002238. Epub 2012 Jun 1.

2.

Spectrum of mutational events in the absence of DOG-1/FANCJ in Caenorhabditis elegans.

Zhao Y, Tarailo-Graovac M, O'Neil NJ, Rose AM.

DNA Repair (Amst). 2008 Nov 1;7(11):1846-54. doi: 10.1016/j.dnarep.2008.07.011. Epub 2008 Aug 30.

PMID:
18708164
3.

Targeted comparative genomic hybridization array for the detection of single- and multiexon gene deletions and duplications.

Tayeh MK, Chin EL, Miller VR, Bean LJ, Coffee B, Hegde M.

Genet Med. 2009 Apr;11(4):232-40. doi: 10.1097/GIM.0b013e318195e191.

PMID:
19282776
5.

Identification and characterization of genes that interact with lin-12 in Caenorhabditis elegans.

Tax FE, Thomas JH, Ferguson EL, Horvitz HR.

Genetics. 1997 Dec;147(4):1675-95.

6.

Mutational accessibility of essential genes on chromosome I(left) in Caenorhabditis elegans.

Johnsen RC, Jones SJ, Rose AM.

Mol Gen Genet. 2000 Mar;263(2):239-52.

PMID:
10778742
7.

Comparison of chromosomal and array-based comparative genomic hybridization for the detection of genomic imbalances in primary prostate carcinomas.

Ribeiro FR, Henrique R, Hektoen M, Berg M, Jerónimo C, Teixeira MR, Lothe RA.

Mol Cancer. 2006 Sep 4;5:33.

8.

Int22h-1/int22h-2-mediated Xq28 rearrangements: intellectual disability associated with duplications and in utero male lethality with deletions.

El-Hattab AW, Fang P, Jin W, Hughes JR, Gibson JB, Patel GS, Grange DK, Manwaring LP, Patel A, Stankiewicz P, Cheung SW.

J Med Genet. 2011 Dec;48(12):840-50. doi: 10.1136/jmedgenet-2011-100125. Epub 2011 Oct 8.

10.

Identification of disease genes by whole genome CGH arrays.

Vissers LE, Veltman JA, van Kessel AG, Brunner HG.

Hum Mol Genet. 2005 Oct 15;14 Spec No. 2:R215-23. Review.

PMID:
16244320
11.

Towards a mutation in every gene in Caenorhabditis elegans.

Moerman DG, Barstead RJ.

Brief Funct Genomic Proteomic. 2008 May;7(3):195-204. doi: 10.1093/bfgp/eln016. Epub 2008 Apr 16. Review.

PMID:
18417533
12.

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
13.

Detection and calibration of microdeletions and microduplications by array-based comparative genomic hybridization and its applicability to clinical genetic testing.

Wong A, Lese Martin C, Heretis K, Ruffalo T, Wilber K, King W, Ledbetter DH.

Genet Med. 2005 Apr;7(4):264-71.

PMID:
15834244
14.

Screening for genomic rearrangements in BRCA1 and BRCA2 genes in Czech high-risk breast/ovarian cancer patients: high proportion of population specific alterations in BRCA1 gene.

Ticha I, Kleibl Z, Stribrna J, Kotlas J, Zimovjanova M, Mateju M, Zikan M, Pohlreich P.

Breast Cancer Res Treat. 2010 Nov;124(2):337-47. doi: 10.1007/s10549-010-0745-y. Epub 2010 Feb 5.

PMID:
20135348
15.

Functional genomic approaches using the nematode Caenorhabditis elegans as a model system.

Lee J, Nam S, Hwang SB, Hong M, Kwon JY, Joeng KS, Im SH, Shim J, Park MC.

J Biochem Mol Biol. 2004 Jan 31;37(1):107-13. Review.

PMID:
14761308
16.

High-throughput isolation of Caenorhabditis elegans deletion mutants.

Liu LX, Spoerke JM, Mulligan EL, Chen J, Reardon B, Westlund B, Sun L, Abel K, Armstrong B, Hardiman G, King J, McCague L, Basson M, Clover R, Johnson CD.

Genome Res. 1999 Sep;9(9):859-67.

17.

Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.

Hannes FD, Sharp AJ, Mefford HC, de Ravel T, Ruivenkamp CA, Breuning MH, Fryns JP, Devriendt K, Van Buggenhout G, Vogels A, Stewart H, Hennekam RC, Cooper GM, Regan R, Knight SJ, Eichler EE, Vermeesch JR.

J Med Genet. 2009 Apr;46(4):223-32. doi: 10.1136/jmg.2007.055202. Epub 2008 Jun 11.

18.

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