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High-resolution array genomic hybridization in prenatal diagnosisFRIEDMAN, J. M.Prenatal diagnosis. 2009, Vol 29, Num 1, pp 20-28, issn 0197-3851, 9 p.Conference Paper

When orthologs diverge between human and mouse : Orthology and ApplicationsGHARIB, Walid H; ROBINSON-RECHAVI, Marc.Briefings in bioinformatics. 2011, Vol 12, Num 5, pp 436-441, issn 1467-5463, 6 p.Article

Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy lossRAJCAN-SEPAROVIC, E; DIEGO-ALVAREZ, D; STEPHENSON, M. D et al.Human reproduction (Oxford. Print). 2010, Vol 25, Num 11, pp 2913-2922, issn 0268-1161, 10 p.Article

Screening of Congenital Heart Disease Patients Using Multiplex Ligation-Dependent Probe Amplification: Early Diagnosis of Syndromic PatientsMEDEN SØRENSEN, Karina; EL-SEGAIER, Milad; WERGE, Thomas et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 4, pp 720-725, issn 1552-4825, 6 p.Article

Annual Research Review: Impact of advances in genetics in understanding developmental psychopathologyADDINGTON, Anjene M; RAPOPORT, Judith L.Journal of child psychology and psychiatry and allied disciplines (Print). 2012, Vol 53, Num 5, pp 510-518, issn 0021-9630, 9 p.Article

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Implications of Genetic Findings for Understanding SchizophreniaOWEN, Michael J.Schizophrenia bulletin. 2012, Vol 38, Num 5, pp 904-907, issn 0586-7614, 4 p.Article

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A new diagnostic workflow for patients with mental retardation and/or multiple congenital abnormalities: test arrays firstGIJSBERS, Antoinet Cj; LEW, Janet Yk; RUIVENKAMP, Claudia Al et al.European journal of human genetics. 2009, Vol 17, Num 11, pp 1394-1402, issn 1018-4813, 9 p.Article

Common Recurrent Microduplication Syndromes: Diagnosis and Management in Clinical Practice : Microduplication syndromesBERG, Jonathan S; POTOCKI, Lorraine; BACINO, Carlos A et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 5, pp 1066-1078, issn 1552-4825, 13 p.Article

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Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohortsMORENO-DE-LUCA, D; SANDERS, S. J; WILLSEY, A. J et al.Molecular psychiatry. 2013, Vol 18, Num 10, pp 1090-1095, issn 1359-4184, 6 p.Article

Epi4K: Gene discovery in 4,000 genomesEpilepsia (Copenhagen). 2012, Vol 53, Num 8, pp 1457-1467, issn 0013-9580, 11 p.Article

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Evolutionary biology looks at behavior geneticsGANGESTAD, Steven W.Personality and individual differences. 2010, Vol 49, Num 4, pp 289-295, issn 0191-8869, 7 p.Article

Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?SHOUKIER, M; KLEIN, N; GRZMIL, P et al.Clinical genetics. 2013, Vol 83, Num 1, pp 53-65, issn 0009-9163, 13 p.Article

Comprehensive copy number variant (CNV) analysis of neuronal pathways genes in psychiatric disorders identifies rare variants within patientsSAUS, Ester; BRUNET, Anna; SORIA, Virginia et al.Journal of psychiatric research. 2010, Vol 44, Num 14, pp 971-978, issn 0022-3956, 8 p.Article

The Genetic Variability and Commonality of Neurodevelopmental DiseaseCOE, Bradley P; GIRIRAJAN, Santhosh; EICHLER, Evan E et al.American journal of medical genetics. Part C, Seminars in medical genetics. 2012, Vol 160, Num 2, pp 118-129, issn 1552-4868, 12 p.Article

Rare Copy Number Variants in Neuropsychiatric Disorders: Specific Phenotype or Not?VAN DEN BOSSCHE, Maarten J; JOHNSTONE, Mandy; SOUERY, Daniel et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2012, Vol 159, Num 7, pp 812-822, issn 1552-4841, 11 p.Article