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

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

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Bibliografiset tiedot
Päätekijät:	Fisher, S, Vargha-Khadem, F, Watkins, K, Monaco, A, Pembrey, M
Aineistotyyppi:	Conference item
Julkaistu:	1997

Samankaltaisia teoksia

Localisation of a gene implicated in a severe speech and language disorder.
Tekijä: Fisher, S, et al.
Julkaistu: (1998)

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

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

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

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

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

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

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

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

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

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

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

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

The genetic basis of a severe speech and language disorder
Tekijä: Fisher, S
Julkaistu: (2003)

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

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

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

Deciphering the genetic basis of speech and language disorders.
Tekijä: Fisher, S, et al.
Julkaistu: (2003)

Familial specific language impairment?
Tekijä: Alcock, K, et al.
Julkaistu: (2000)

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

Language after acquired unilateral pathology and hemispherectomy
Tekijä: Liegeois, F, et al.
Julkaistu: (2000)

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

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

On genes, speech, and language.
Tekijä: Fisher, S
Julkaistu: (2005)

Molecular genetics of speech and language disorders.
Tekijä: Newbury, D, et al.
Julkaistu: (2002)

MOLECULAR WINDOWS INTO SPEECH AND LANGUAGE DISORDERS
Tekijä: Fisher, S
Julkaistu: (2011)

Molecular windows into speech and language disorders.
Tekijä: Fisher, S
Julkaistu: (2007)

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

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

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

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

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

Dissection of molecular mechanisms underlying speech and language disorders
Tekijä: Fisher, S
Julkaistu: (2005)

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

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

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

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

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

Speech and Language Disorders
Tekijä: Bishop, D, et al.
Julkaistu: (2009)

Geriatrie Speech and Language Disorders
Tekijä: Hashem Shemshadi, et al.
Julkaistu: (2006-10-01)