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Search for loss of heterozygosity and mutation analysis of KRIT1 gene in CCM patientsMARINI, Valeria; FERRERA, Loretta; PIGATTO, Francesca et al.American journal of medical genetics. 2004, Vol 130A, Num 1, pp 98-101, issn 0148-7299, 4 p.Article

Germline DICER 1 mutation and associated loss of heterozygosity in a pineoblastomaSABBAGHIAN, Nelly; HAZEL, Nancy; SRIVASTAVA, Archana et al.Journal of medical genetics. 2012, Vol 49, Num 7, pp 417-419, issn 0022-2593, 3 p.Article

Effect of nucleophosmin1 haploinsufficiency on hematopoietic stem cellsRAVAL, A; KUSLER, B; PANG, W. W et al.Leukemia. 2012, Vol 26, Num 4, pp 853-855, issn 0887-6924, 3 p.Article

Loss of heterozygosity in human skinHAPPLE, R.Journal of the American Academy of Dermatology. 1999, Vol 41, Num 2, pp 143-161, issn 0190-9622, 1Article

Large-scale allelotype of pancreaticobiliary carcinoma provides quantitative estimates of genome-wide allelic lossIACOBUZIO-DONAHUE, Christine A; VAN DER HEIJDEN, Michiel S; KERN, Scott E et al.Cancer research (Baltimore). 2004, Vol 64, Num 3, pp 871-875, issn 0008-5472, 5 p.Article

Early-onset colorectal cancer with stable microsatellite DNA and near-diploid chromosomesTSUN LEUNG CHAN; CURTIS, Lucy C; SIU TSAN YUEN et al.Oncogene (Basingstoke). 2001, Vol 20, Num 35, pp 4871-4876, issn 0950-9232Article

Loss of heterozygosity analysis defines a 3-cM region of 15q commonly deleted in human malignant mesotheliomaDE RIENZO, Assunta; BALSARA, Binaifer R; APOSTOLOU, Sinoula et al.Oncogene (Basingstoke). 2001, Vol 20, Num 43, pp 6245-6249, issn 0950-9232Article

NPM-MLF1 synergizes with Npm haploinsufficiency to enhance myeloid progenitor activityLEE, W.-H; SALEK-ARDAKANI, S; PANDOLFI, P. P et al.Leukemia. 2012, Vol 26, Num 5, pp 1110-1112, issn 0887-6924, 3 p.Article

Haploinsufficiency of RAD51B causes centrosome fragmentation and aneuploidy in human cellsDATE, Osamu; KATSURA, Mari; ISHIDA, Mari et al.Cancer research (Baltimore). 2006, Vol 66, Num 12, pp 6018-6024, issn 0008-5472, 7 p.Article

Rb1 Haploinsufficiency Promotes Telomere Attrition and Radiation-Induced Genomic InstabilityGONZALEZ-VASCONCELLOS, Iria; ANASTASOV, Natasa; SANLI-BONAZZI, Bahar et al.Cancer research (Chicago, Ill.). 2013, Vol 73, Num 14, pp 4247-4255, issn 0008-5472, 9 p.Article

Loss of heterozygosity in 7q myeloid disorders: clinical associations and genomic pathogenesisJEREZ, Andres; SUGIMOTO, Yuka; KULASEKARARAJ, Austin G et al.Blood. 2012, Vol 119, Num 25, pp 6109-6117, issn 0006-4971, 9 p.Article

Genome-wide analysis of DNA copy number changes and LOH in CLL using high-density SNP arraysPFEIFER, Dietmar; PANTIC, Milena; SKATULLA, Ilona et al.Blood. 2007, Vol 109, Num 3, pp 1202-1210, issn 0006-4971, 9 p.Article

LOH-proficient embryonic stem cells : a model of cancer progenitor cells?BIELAS, Jason H; VENKATESAN, Ranga N; LOEB, Lawrence A et al.Trends in genetics (Regular ed.). 2007, Vol 23, Num 4, pp 154-157, issn 0168-9525, 4 p.Article

Loss of heterozygosity and its correlation with expression profiles in subclasses of invasive breast cancersWANG, Zhigang C; MING LIN; IGLEHART, James D et al.Cancer research (Baltimore). 2004, Vol 64, Num 1, pp 64-71, issn 0008-5472, 8 p.Article

Loss of heterozygosity on chromosome 4q32-35 in sporadic basal cell carcinomas: evidence for the involvement of p33ING2/ING1L and SAP30 genesSIRONI, Elena; CERRI, Amilcare; TOMASINI, Dario et al.Journal of cutaneous pathology. 2004, Vol 31, Num 4, pp 318-322, issn 0303-6987, 5 p.Article

SF3B1 haploinsufficiency leads to formation of ring sideroblasts in myelodysplastic syndromesVISCONTE, Valeria; ROGERS, Heesun J; JEREZ, Andres et al.Blood. 2012, Vol 120, Num 16, pp 3173-3186, issn 0006-4971, 14 p.Article

Isolated haploinsufficiency of exon 1 of the SHOX gene in a patient with idiopathic short statureTAN, Y.-M; LOKE, K.-Y.Journal of clinical pathology. 2006, Vol 59, Num 7, pp 773-774, issn 0021-9746, 2 p.Article

New evaluation of plasma DNA microsatellite analysis in patients with TCC of the urinary bladderFORNARI, Delfina; STEVEN, Kenneth; HANSEN, Alastair B et al.Anticancer research. 2004, Vol 24, Num 3A, pp 1733-1736, issn 0250-7005, 4 p.Article

Loss of heterozygosity and immunohistochemistry of adenocarcinomas of the esophagus and gastric cardiaMARSMAN, Willem A; BIRJMOHUN, Rakesh S; VAN REES, Bastiaan P et al.Clinical cancer research. 2004, Vol 10, Num 24, pp 8479-8485, issn 1078-0432, 7 p.Article

An age-induced switch to a hyper-recombinational stateMCMURRAY, Michael A; GOMCHLING, Daniel E.Science (Washington, D.C.). 2003, Vol 301, Num 5641, pp 1908-1911, issn 0036-8075, 4 p.Article

Chromosome 22q a frequent site of allele loss in head and neck carcinomaPOLI-FREDERICO, R. C; BERGAMO, N. A; REIS, P. P et al.Head & neck. 2000, Vol 22, Num 6, pp 585-590, issn 1043-3074Article

Molecular analysis of alterations of the p18^INK4c gene in human meningiomasSANTARIUS, T; KIRSCH, M; NIKAS, D. C et al.Neuropathology and applied neurobiology (Print). 2000, Vol 26, Num 1, pp 67-75, issn 0305-1846Article

Low frequency of genetic change in p53 immunopositive clones in human epidermisTABATA, H; NAGANO, T; RAY, A. J et al.Journal of investigative dermatology. 1999, Vol 113, Num 6, pp 972-976, issn 0022-202XConference Paper

PCR-based genotyping can generate artifacts in LOH analysesBLUTEAU, O; LEGOIX, P; LAURENT-PUIG, P et al.BioTechniques. 1999, Vol 27, Num 6, pp 1100-1102, issn 0736-6205Article