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Duplication of the entire 22.9 Mb human chromosome 21 syntenic region on mouse chromosome 16 causes cardiovascular and gastrointestinal abnormalitiesZHONGYOU LI; TAO YU; MORISHIMA, Masae et al.Human molecular genetics (Print). 2007, Vol 16, Num 11, pp 1359-1366, issn 0964-6906, 8 p.Article

Identification of large-scale human-specific copy number differences by inter-species array comparative genomic hybridizationGOIDTS, Violaine; ARMENGOL, Lluis; HAMEISTER, Horst et al.Human genetics. 2006, Vol 119, Num 1-2, pp 185-198, issn 0340-6717, 14 p.Article

Array comparative genomic hybridisation of 52 subjects with a Smith—Magenis—like phenotype: identification of dosage sensitive loci also associated with schizophrenia, autism, and developmental delayWILLIAMS, Stephen R; GIRIRAJAN, Santhosh; TEGAY, David et al.Journal of medical genetics. 2010, Vol 47, Num 4, pp 223-229, issn 0022-2593, 7 p.Article

Novel karyotypic changes detected by comparative genomic hybridization in a case of congenital cervical immature teratomaMILIARAS, Dimosthenis; GRIMBIZIS, Grigoris; CONROY, Jeffrey et al.Birth defects research. Clinical and molecular teratology. 2005, Vol 73, Num 8, pp 572-576, issn 1542-0752, 5 p.Article

A comparative analysis of two tissue procurement approaches for the genomic profiling of clinical colorectal cancer samplesMOJICA, Wilfrido D; SYKES, Donald E; CONROY, Jeffrey et al.International journal of colorectal disease (Print). 2008, Vol 23, Num 11, pp 1089-1098, issn 0179-1958, 10 p.Article

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Array-Comparative Genomic Hybridization Analysis of Primary Endometrial and Ovarian High-grade Neuroendocrine Carcinoma Associated With Adenocarcinoma : Mystery Resolved?MHAWECH-FAUCEGLIA, Paulette; ODUNSI, Kunle; DIM, Daniel et al.International journal of gynecological pathology. 2008, Vol 27, Num 4, pp 539-546, issn 0277-1691, 8 p.Article

Loss of breast cancer metastasis suppressor 1 protein expression predicts reduced disease-free survival in subsets of breast cancer patientsHICKS, David G; YODER, Brian J; CHOUEIRI, Toni K et al.Clinical cancer research. 2006, Vol 12, Num 22, pp 6702-6708, issn 1078-0432, 7 p.Article

Haplotypes and haplotype-pairs of IL-1 beta and IL-6 genes and risk of non fatal myocardial infarction in the Western New York Acute MI StudyDE GAETANO, Monica; QUACQUARUCCIO, Gianni; DI CASTEINUOVO, Augusto et al.Thrombosis and haemostasis. 2011, Vol 106, Num 6, pp 1231-1233, issn 0340-6245, 3 p.Article

Manipulation of nonsense mediated decay identifies gene mutations in colon cancer cells with microsatellite instabilityIONOV, Yurij; NOWAK, Norma; PERUCHO, Manuel et al.Oncogene (Basingstoke). 2004, Vol 23, Num 3, pp 639-645, issn 0950-9232, 7 p.Article

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Familial 4.3 Mb duplication of 21q22 sheds new light on the down syndrome critical regionRONAN, Anne; FAGAN, Kerry; CHRISTIE, Louise et al.Journal of medical genetics. 2007, Vol 44, Num 7, pp 448-451, issn 0022-2593, 4 p.Article

Analytical and Clinical Validity of Whole-Genome Oligonucleotide Array Comparative Genomic Hybridization for Pediatric Patients With Mental Retardation and Developmental DelayBIXIA XIANG; AO LI; VALENTIN, Dinu et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 15, pp 1942-1954, issn 1552-4825, 13 p.Article

Identification of metastasis-associated breast cancer genes using a high-resolution whole genome profiling approachDESOUKI, Mohamed M; SHAOXI LIAO; HUAYI HUANG et al.Journal of cancer research and clinical oncology. 2011, Vol 137, Num 5, pp 795-809, issn 0171-5216, 15 p.Article

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Lipid in the livers of adolescents with nonalcoholic steatohepatitis: combined effects of pathways on steatosisLIXIN ZHU; BAKER, Susan S; WENSHENG LIU et al.Metabolism, clinical and experimental. 2011, Vol 60, Num 7, pp 1001-1011, issn 0026-0495, 11 p.Article

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Recurrent 16p11.2 microdeletions in autismKUMAR, Ravinesh A; KARAMOHAMED, Samer; CHRISTIAN, Susan L et al.Human molecular genetics (Print). 2008, Vol 17, Num 4, pp 628-638, issn 0964-6906, 11 p.Article

Phase 1 Study of Arsenic Trioxide, High-Dose Cytarabine, and Idarubicin to Down-Regulate Constitutive Signal Transducer and Activator of Transcription 3 Activity in Patients Aged <60 Years With Acute Myeloid LeukemiaWETZLER, Meir; ANDREWS, Chris; BAUMANN, Heinz et al.Cancer. 2011, Vol 117, Num 21, pp 4861-4868, issn 0008-543X, 8 p.Article

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A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autismKUMAR, Ravinesh A; SUDI, Jyotsna; BABATZ, Timothy D et al.Journal of medical genetics. 2010, Vol 47, Num 2, pp 81-90, issn 0022-2593, 10 p.Article

Smith-magenis syndrome and moyamoya disease in a patient with del(17)(p11.2p13.1)GIRIRAJAN, Santhosh; MENDOZA-LONDONO, Roberto; VLANGOS, Christopher N et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 9, pp 999-1008, issn 1552-4825, 10 p.Article

Molecular Karyotypes of Hodgkin and Reed―Sternberg Cells at Disease Onset Reveal Distinct Copy Number Alterations in Chemosensitive versus Refractory Hodgkin LymphomaSLOVAK, Marilyn L; BEDELL, Victoria; HSU, Ya-Hsuan et al.Clinical cancer research (Print). 2011, Vol 17, Num 10, pp 3443-3454, issn 1078-0432, 12 p.Article