Localisation of a gene implicated in a severe speech and language disorder.

Localisation of a gene implicated in a severe speech and language disorder.

Toon andere (1) versies

Between 2 and 5% of children who are otherwise unimpaired have significant difficulties in acquiring expressive and/or receptive language, despite adequate intelligence and opportunity. While twin studies indicate a significant role for genetic factors in developmental disorders of speech and langua...

Volledige beschrijving

Bibliografische gegevens
Hoofdauteurs:	Fisher, S, Vargha-Khadem, F, Watkins, K, Monaco, A, Pembrey, M
Formaat:	Journal article
Taal:	English
Gepubliceerd in:	1998

Gelijkaardige items

Localisation of a gene implicated in a severe speech and language disorder.
door: Fisher, S, et al.
Gepubliceerd in: (1997)

A forkhead-domain gene is mutated in a severe speech and language disorder.
door: Lai, C, et al.
Gepubliceerd in: (2001)

A novel forkhead-domain gene is mutated in a severe speech and language disorder.
door: Fisher, S, et al.
Gepubliceerd in: (2001)

A novel transcription factor is mutated in a severe speech and language disorder
door: Lai, C, et al.
Gepubliceerd in: (2001)

Functional and structural brain abnormalities associated with a genetic disorder of speech and language.
door: Watkins, K, et al.
Gepubliceerd in: (1999)

Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia.
door: Watkins, K, et al.
Gepubliceerd in: (2002)

Neural basis of an inherited speech and language disorder.
door: Vargha-Khadem, F, et al.
Gepubliceerd in: (1998)

Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder.
door: Vargha-Khadem, F, et al.
Gepubliceerd in: (1995)

Pitch and timing abilities in inherited speech and language impairment.
door: Alcock, K, et al.
Gepubliceerd in: (2000)

Oral dyspraxia in inherited speech and language impairment and acquired dysphasia.
door: Alcock, K, et al.
Gepubliceerd in: (2000)

Neocerebellar Crus I abnormalities associated with a speech and language disorder due to a mutation in FOXP2
door: Argyropoulos, G, et al.
Gepubliceerd in: (2018)

MRI analysis of an inherited speech and language disorder: structural brain abnormalities.
door: Watkins, K, et al.
Gepubliceerd in: (2002)

Structural abnormalities revealed by analysis of magnetic resonance brain images in a large family with an inherited speech and language disorder
door: Watkins, K, et al.
Gepubliceerd in: (1997)

The genetic basis of a severe speech and language disorder
door: Fisher, S
Gepubliceerd in: (2003)

Identification of foxp2 truncation as a novel cause of developmental speech disorder.
door: MacDermot, K, et al.
Gepubliceerd in: (2004)

The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder.
door: Lai, C, et al.
Gepubliceerd in: (2000)

Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits.
door: MacDermot, K, et al.
Gepubliceerd in: (2005)

Deciphering the genetic basis of speech and language disorders.
door: Fisher, S, et al.
Gepubliceerd in: (2003)

Familial specific language impairment?
door: Alcock, K, et al.
Gepubliceerd in: (2000)

Developmental disorders of speech and language: from genes to brain structure and function.
door: Watkins, K
Gepubliceerd in: (2011)

Language after acquired unilateral pathology and hemispherectomy
door: Liegeois, F, et al.
Gepubliceerd in: (2000)

FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder.
door: Lai, C, et al.
Gepubliceerd in: (2003)

Functional genetic analysis of mutations implicated in a human speech and language disorder.
door: Vernes, S, et al.
Gepubliceerd in: (2006)

On genes, speech, and language.
door: Fisher, S
Gepubliceerd in: (2005)

Molecular genetics of speech and language disorders.
door: Newbury, D, et al.
Gepubliceerd in: (2002)

MOLECULAR WINDOWS INTO SPEECH AND LANGUAGE DISORDERS
door: Fisher, S
Gepubliceerd in: (2011)

Molecular windows into speech and language disorders.
door: Fisher, S
Gepubliceerd in: (2007)

Genetic advances in the study of speech and language disorders.
door: Newbury, D, et al.
Gepubliceerd in: (2010)

Molecular evolution of FOXP2, a gene involved in speech and language.
door: Enard, W, et al.
Gepubliceerd in: (2002)

Aberrant striatal activity in mice with a mutation implicated in a developmental speech and language disorder
door: French, C, et al.
Gepubliceerd in: (2010)

Severely impaired episodic memory after early hypoxic-ischaemic injury
door: Gadian, D, et al.
Gepubliceerd in: (1999)

Neural basis of speech and language impairments in development: the case of developmental language disorder
door: Asaridou, SS, et al.
Gepubliceerd in: (2022)

Dissection of molecular mechanisms underlying speech and language disorders
door: Fisher, S
Gepubliceerd in: (2005)

Dual language intervention in a case of severe speech sound disorder
door: Eliane Ramos, et al.
Gepubliceerd in: (2014-06-01)

Dual language intervention in a case of severe speech sound disorder
door: Eliane Ramos, et al.
Gepubliceerd in: (2014-11-01)

Co-localisation of abnormal brain structure and funtion in Specific Language Impairment
door: Badcock, N, et al.
Gepubliceerd in: (2012)

Co-localisation of abnormal brain structure and function in specific language impairment.
door: Badcock, N, et al.
Gepubliceerd in: (2012)

Co-localisation of abnormal brain structure and function in specific language impairment
door: Badcock, N, et al.
Gepubliceerd in: (2012)

Speech and Language Disorders
door: Bishop, D, et al.
Gepubliceerd in: (2009)

Geriatrie Speech and Language Disorders
door: Hashem Shemshadi, et al.
Gepubliceerd in: (2006-10-01)