Complex nature of apparently balanced chromosomal rearrangements in patients with autism spectrum disorder. - Wikidata - awgldk - TriplyDB

Complex nature of apparently balanced chromosomal rearrangements in patients with autism spectrum disorder.

Complex nature of apparently balanced chromosomal rearrangements in patients with autism spectrum disorder.

http://www.wikidata.org/entity/Q35257406

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Mechanisms of Origin, Phenotypic Effects and Diagnostic Implications of Complex Chromosome Rearrangements PARP3 is a promoter of chromosomal rearrangements and limits G4 DNA.Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome.The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies.Prenatal diagnosis by chromosomal microarray analysis.Array-CGH Analysis in a Cohort of Phenotypically Well-Characterized Individuals with "Essential" Autism Spectrum Disorders.A rapid and reliable chromosome analysis method for products of conception using interphase nuclei.Deletion 2q37 syndrome: Cognitive-behavioral trajectories and autistic features related to breakpoint and deletion size.Current Enlightenment About Etiology and Pharmacological Treatment of Autism Spectrum Disorder.

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P2860

Complex nature of apparently balanced chromosomal rearrangements in patients with autism spectrum disorder.

http://www.wikidata.org/entity/Q35257406

description

2015 nî lūn-bûn

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2015 թվականի մարտին հրատարակված գիտական հոդված

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2015年の論文

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name

Complex nature of apparently b ...... with autism spectrum disorder.

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Complex nature of apparently b ...... with autism spectrum disorder.

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Complex nature of apparently b ...... with autism spectrum disorder.

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Complex nature of apparently b ...... with autism spectrum disorder.

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Complex nature of apparently b ...... with autism spectrum disorder.

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Complex nature of apparently b ...... with autism spectrum disorder.

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Molecular Autism

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Complex nature of apparently b ...... with autism spectrum disorder.

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Andrée Delahaye

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Anne-Claude Tabet

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Aurelia Jacquette

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Azzedine Aboura

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Brigitte Benzacken

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Céline Dupont

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Delphine Héron

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Elsa Delaby

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Françoise Devillard

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Gudrun Nygren

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P2860

Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5qter and 9qter

Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding

Molecular analysis of 20 patients with 2q37.3 monosomy: definition of minimum deletion intervals for key phenotypes

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

The transcription factor RFX3 directs nodal cilium development and left-right asymmetry specification

The 2q37-deletion syndrome: an update of the clinical spectrum including overweight, brachydactyly and behavioural features in 14 new patients

Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting

De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.

Haploinsufficiency of HDAC4 causes brachydactyly mental retardation syndrome, with brachydactyly type E, developmental delays, and behavioral problems.

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Christopher Gillberg

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Richard Delorme

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2015-03-25T00:00:00Z

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Autism spectrum

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