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

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

Бусад хувилбаруудыг харуулах (1)

Номзүйн дэлгэрэнгүй
Үндсэн зохиолчид:	Fisher, S, Vargha-Khadem, F, Watkins, K, Monaco, A, Pembrey, M
Формат:	Conference item
Хэвлэсэн:	1997

Ижил төстэй зүйлс

Localisation of a gene implicated in a severe speech and language disorder.
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A forkhead-domain gene is mutated in a severe speech and language disorder.
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A novel forkhead-domain gene is mutated in a severe speech and language disorder.
-н: Fisher, S, зэрэг
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A novel transcription factor is mutated in a severe speech and language disorder
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Functional and structural brain abnormalities associated with a genetic disorder of speech and language.
-н: Watkins, K, зэрэг
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Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia.
-н: Watkins, K, зэрэг
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Neural basis of an inherited speech and language disorder.
-н: Vargha-Khadem, F, зэрэг
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Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder.
-н: Vargha-Khadem, F, зэрэг
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Pitch and timing abilities in inherited speech and language impairment.
-н: Alcock, K, зэрэг
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Oral dyspraxia in inherited speech and language impairment and acquired dysphasia.
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Neocerebellar Crus I abnormalities associated with a speech and language disorder due to a mutation in FOXP2
-н: Argyropoulos, G, зэрэг
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MRI analysis of an inherited speech and language disorder: structural brain abnormalities.
-н: Watkins, K, зэрэг
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Structural abnormalities revealed by analysis of magnetic resonance brain images in a large family with an inherited speech and language disorder
-н: Watkins, K, зэрэг
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The genetic basis of a severe speech and language disorder
-н: Fisher, S
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Identification of foxp2 truncation as a novel cause of developmental speech disorder.
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The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder.
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Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits.
-н: MacDermot, K, зэрэг
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Deciphering the genetic basis of speech and language disorders.
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Familial specific language impairment?
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Developmental disorders of speech and language: from genes to brain structure and function.
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Language after acquired unilateral pathology and hemispherectomy
-н: Liegeois, F, зэрэг
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FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder.
-н: Lai, C, зэрэг
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Functional genetic analysis of mutations implicated in a human speech and language disorder.
-н: Vernes, S, зэрэг
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On genes, speech, and language.
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Molecular genetics of speech and language disorders.
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MOLECULAR WINDOWS INTO SPEECH AND LANGUAGE DISORDERS
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Molecular windows into speech and language disorders.
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Genetic advances in the study of speech and language disorders.
-н: Newbury, D, зэрэг
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Molecular evolution of FOXP2, a gene involved in speech and language.
-н: Enard, W, зэрэг
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Aberrant striatal activity in mice with a mutation implicated in a developmental speech and language disorder
-н: French, C, зэрэг
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Severely impaired episodic memory after early hypoxic-ischaemic injury
-н: Gadian, D, зэрэг
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Neural basis of speech and language impairments in development: the case of developmental language disorder
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Dissection of molecular mechanisms underlying speech and language disorders
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Dual language intervention in a case of severe speech sound disorder
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Dual language intervention in a case of severe speech sound disorder
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Co-localisation of abnormal brain structure and funtion in Specific Language Impairment
-н: Badcock, N, зэрэг
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Co-localisation of abnormal brain structure and function in specific language impairment.
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Co-localisation of abnormal brain structure and function in specific language impairment
-н: Badcock, N, зэрэг
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Speech and Language Disorders
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Geriatrie Speech and Language Disorders
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