Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder
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Ravinesh A. Kumar | S. Christian | E. Cook | N. Nowak | T. Gilliam | E. Hatchwell | E. Gershon | J. Badner | N. Nowak | J. Conroy | W. Dobyns | S. Matsui | Camille W. Brune | S. Karamohamed | Jyotsna Sudi | Shaung Liu | Seiichi Matsui | Devin E. Mcquaid | James Gergel | Devin E Mcquaid | Devin E McQuaid | Samer Karamohamed
[1] D. Conrad,et al. Recurrent 16p11.2 microdeletions in autism. , 2007, Human molecular genetics.
[2] Kenny Q. Ye,et al. Strong Association of De Novo Copy Number Mutations with Autism , 2007, Science.
[3] Thomas Bourgeron,et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements , 2007, Nature Genetics.
[4] A. Alberti,et al. 1.5 Mb de novo 22q11.21 microduplication in a patient with cognitive deficits and dysmorphic facial features , 2007, Clinical genetics.
[5] N. M. Mukaddes,et al. Autistic disorder and 22q11.2 duplication , 2007 .
[6] Kiyoko F. Aoki-Kinoshita,et al. Gene annotation and pathway mapping in KEGG. , 2007, Methods in molecular biology.
[7] L. Feuk,et al. Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome , 2006, Cytogenetic and Genome Research.
[8] E. Mickelson,et al. Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1 , 2006, Journal of Medical Genetics.
[9] P. Jonveaux,et al. Pure de-novo 5 Mb duplication at Xp11.22-p11.23 in a male: phenotypic and molecular characterization , 2006, Journal of Human Genetics.
[10] R Redon,et al. Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders , 2006, Journal of Medical Genetics.
[11] M. V. Van Allen,et al. 15q Duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array‐CGH , 2006, Clinical genetics.
[12] Eric Fombonne,et al. Epidemiology of autistic disorder and other pervasive developmental disorders. , 2005, The Journal of clinical psychiatry.
[13] Jane Lomax,et al. Get ready to GO! A biologist's guide to the Gene Ontology , 2005, Briefings Bioinform..
[14] M. Portnoï,et al. 22q11.2 duplication syndrome: Two new familial cases with some overlapping features with DiGeorge/velocardiofacial syndromes , 2005, American journal of medical genetics. Part A.
[15] D. Albertson,et al. The BAC Resource: Tools for Array CGH and FISH , 2005, Current protocols in human genetics.
[16] Eric Fombonne,et al. Pervasive developmental disorders in preschool children: confirmation of high prevalence. , 2005, The American journal of psychiatry.
[17] E. Mickelson,et al. A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3‐25 detected using whole genomic array CGH , 2005, Clinical genetics.
[18] Michael Krauthammer,et al. GeneWays: a system for extracting, analyzing, visualizing, and integrating molecular pathway data , 2004, J. Biomed. Informatics.
[19] S. Folstein,et al. Genetics of austim: complex aetiology for a heterogeneous disorder , 2001, Nature Reviews Genetics.
[20] S. Spence,et al. The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions. , 2001, American journal of human genetics.
[21] N. Dracopoli,et al. Current protocols in human genetics , 1994 .
[22] L. Kanner. Autistic disturbances of affective contact. , 1968, Acta paedopsychiatrica.
[23] J. Raven. Coloured progressive matrices : sets A, Ab, B , 1956 .