11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structures.

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Jacobsen Syndrome: Surgical Complications due to Unsuspected Diagnosis, the Importance of Molecular Studies in Patients with Craniosynostosis.Ventriculomegaly and cerebellar hypoplasia in a neonate with interstitial 11q 24 deletion in Jacobsen syndrome region.

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11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structures.

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11q24.2-25 micro-rearrangement ...... Relation to brain structures.

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11q24.2-25 micro-rearrangement ...... Relation to brain structures.

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11q24.2-25 micro-rearrangement ...... Relation to brain structures.

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11q24.2-25 micro-rearrangement ...... Relation to brain structures.

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11q24.2-25 micro-rearrangement ...... Relation to brain structures.

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11q24.2-25 micro-rearrangement ...... Relation to brain structures.

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P1476

11q24.2-25 micro-rearrangement ...... Relation to brain structures.

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P2093

Alexandre Mathieu

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Anita Beggiato

http://www.w3.org/2001/XMLSchema#string

Anna Maruani

http://www.w3.org/2001/XMLSchema#string

Claire S Leblond

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Frederique Amsellem

http://www.w3.org/2001/XMLSchema#string

Guillaume Huguet

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Nathalie Lemière

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P2860

Submicroscopic deletions of 11q24-25 in individuals without Jacobsen syndrome: re-examination of the critical region by high-resolution array-CGH

Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

Screening of chondrogenic factors with a real-time fluorescence-monitoring cell line ATDC5-C2ER: identification of sorting nexin 19 as a novel factor

Role of the Rho GTPase-activating protein RICS in neurite outgrowth

Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome

Functional impact of global rare copy number variation in autism spectrum disorders

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism

Sorting nexin 3 (SNX3) is disrupted in a patient with a translocation t(6;13)(q21;q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype

Sorting nexin-2 is associated with tubular elements of the early endosome, but is not essential for retromer-mediated endosome-to-TGN transport

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3019-3030

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scholarly article

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10.1002/AJMG.A.37345

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English

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http://www.w3.org/2001/XMLSchema#string

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167A

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Christopher Gillberg

Thomas Bourgeron

Monique Elmaleh-bergès

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2015-09-03T00:00:00Z

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281541413

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26334118

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P921

Autism spectrum

autism

11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structures.

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P2860

P2860

11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structures.

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