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

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

عرض إصدارات أخرى (1)

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Fisher, S, Vargha-Khadem, F, Watkins, K, Monaco, A, Pembrey, M
التنسيق:	Conference item
منشور في:	1997

مواد مشابهة

Localisation of a gene implicated in a severe speech and language disorder.
حسب: Fisher, S, وآخرون
منشور في: (1998)

A forkhead-domain gene is mutated in a severe speech and language disorder.
حسب: Lai, C, وآخرون
منشور في: (2001)

A novel forkhead-domain gene is mutated in a severe speech and language disorder.
حسب: Fisher, S, وآخرون
منشور في: (2001)

A novel transcription factor is mutated in a severe speech and language disorder
حسب: Lai, C, وآخرون
منشور في: (2001)

Functional and structural brain abnormalities associated with a genetic disorder of speech and language.
حسب: Watkins, K, وآخرون
منشور في: (1999)

Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia.
حسب: Watkins, K, وآخرون
منشور في: (2002)

Neural basis of an inherited speech and language disorder.
حسب: Vargha-Khadem, F, وآخرون
منشور في: (1998)

Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder.
حسب: Vargha-Khadem, F, وآخرون
منشور في: (1995)

Pitch and timing abilities in inherited speech and language impairment.
حسب: Alcock, K, وآخرون
منشور في: (2000)

Oral dyspraxia in inherited speech and language impairment and acquired dysphasia.
حسب: Alcock, K, وآخرون
منشور في: (2000)

Neocerebellar Crus I abnormalities associated with a speech and language disorder due to a mutation in FOXP2
حسب: Argyropoulos, G, وآخرون
منشور في: (2018)

MRI analysis of an inherited speech and language disorder: structural brain abnormalities.
حسب: Watkins, K, وآخرون
منشور في: (2002)

Structural abnormalities revealed by analysis of magnetic resonance brain images in a large family with an inherited speech and language disorder
حسب: Watkins, K, وآخرون
منشور في: (1997)

The genetic basis of a severe speech and language disorder
حسب: Fisher, S
منشور في: (2003)

Identification of foxp2 truncation as a novel cause of developmental speech disorder.
حسب: MacDermot, K, وآخرون
منشور في: (2004)

The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder.
حسب: Lai, C, وآخرون
منشور في: (2000)

Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits.
حسب: MacDermot, K, وآخرون
منشور في: (2005)

Deciphering the genetic basis of speech and language disorders.
حسب: Fisher, S, وآخرون
منشور في: (2003)

Familial specific language impairment?
حسب: Alcock, K, وآخرون
منشور في: (2000)

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

Language after acquired unilateral pathology and hemispherectomy
حسب: Liegeois, F, وآخرون
منشور في: (2000)

FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder.
حسب: Lai, C, وآخرون
منشور في: (2003)

Functional genetic analysis of mutations implicated in a human speech and language disorder.
حسب: Vernes, S, وآخرون
منشور في: (2006)

On genes, speech, and language.
حسب: Fisher, S
منشور في: (2005)

Molecular genetics of speech and language disorders.
حسب: Newbury, D, وآخرون
منشور في: (2002)

MOLECULAR WINDOWS INTO SPEECH AND LANGUAGE DISORDERS
حسب: Fisher, S
منشور في: (2011)

Molecular windows into speech and language disorders.
حسب: Fisher, S
منشور في: (2007)

Genetic advances in the study of speech and language disorders.
حسب: Newbury, D, وآخرون
منشور في: (2010)

Molecular evolution of FOXP2, a gene involved in speech and language.
حسب: Enard, W, وآخرون
منشور في: (2002)

Aberrant striatal activity in mice with a mutation implicated in a developmental speech and language disorder
حسب: French, C, وآخرون
منشور في: (2010)

Severely impaired episodic memory after early hypoxic-ischaemic injury
حسب: Gadian, D, وآخرون
منشور في: (1999)

Neural basis of speech and language impairments in development: the case of developmental language disorder
حسب: Asaridou, SS, وآخرون
منشور في: (2022)

Dissection of molecular mechanisms underlying speech and language disorders
حسب: Fisher, S
منشور في: (2005)

Dual language intervention in a case of severe speech sound disorder
حسب: Eliane Ramos, وآخرون
منشور في: (2014-06-01)

Dual language intervention in a case of severe speech sound disorder
حسب: Eliane Ramos, وآخرون
منشور في: (2014-11-01)

Co-localisation of abnormal brain structure and funtion in Specific Language Impairment
حسب: Badcock, N, وآخرون
منشور في: (2012)

Co-localisation of abnormal brain structure and function in specific language impairment.
حسب: Badcock, N, وآخرون
منشور في: (2012)

Co-localisation of abnormal brain structure and function in specific language impairment
حسب: Badcock, N, وآخرون
منشور في: (2012)

Speech and Language Disorders
حسب: Bishop, D, وآخرون
منشور في: (2009)

Geriatrie Speech and Language Disorders
حسب: Hashem Shemshadi, وآخرون
منشور في: (2006-10-01)