Literature DB >> 2332125

An extended family with a dominantly inherited speech disorder.

J A Hurst1, M Baraitser, E Auger, F Graham, S Norell.   

Abstract

A three-generation family is described in which 16 members have a severe developmental verbal dyspraxia. Inheritance is autosomal dominant, with full penetrance. Intelligence and hearing are normal.

Entities:  

Mesh：

Year:  1990        PMID： 2332125     DOI： 10.1111/j.1469-8749.1990.tb16948.x

Source DB:  PubMed          Journal:  Dev Med Child Neurol        ISSN： 0012-1622            Impact factor:   5.449


  62 in total

Review 1.  Functional and structural brain abnormalities associated with a genetic disorder of speech and language.

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Review 4.  The human lexinome: genes of language and reading.

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6.  A genome-wide sib-pair scan for quantitative language traits reveals linkage to chromosomes 10 and 13.

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Journal:  Genes Brain Behav       Date:  2015-06       Impact factor: 3.449

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Review 8.  Autism: in search of susceptibility genes.

Authors:  Janine A Lamb; Jeremy R Parr; Anthony J Bailey; Anthony P Monaco
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9.  Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.

Authors:  Gordana Raca; Becky S Baas; Salman Kirmani; Jennifer J Laffin; Craig A Jackson; Edythe A Strand; Kathy J Jakielski; Lawrence D Shriberg
Journal:  Eur J Hum Genet       Date:  2012-08-22       Impact factor: 4.246

10.  Striatal FoxP2 is actively regulated during songbird sensorimotor learning.

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Journal:  PLoS One       Date:  2010-01-06       Impact factor: 3.240
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