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Volumn 67, Issue 2, 2000, Pages 357-368

The SPCH1 region on human 7q31: Genomic characterization of the critical interval and localization of translocations associated with speech and language disorder

(12) Lai, Cecilia S L a Fisher, Simon E a Hurst, Jane A b Levy, Elaine R a Hodgson, Shirley c Fox, Margaret d Jeremiah, Stephen d Povey, Susan d Jamison, D Curtis e Green, Eric D e Vargha Khadem, Faraneh f Monaco, Anthony P a

a UNIVERSITY OF OXFORD (United Kingdom)

b OXFORD UNIVERSITY HOSPITALS NHS FOUNDATION TRUST (United Kingdom)

c GUY S HOSPITAL (United Kingdom)

d UNIVERSITY COLLEGE LONDON (United Kingdom)

e NATIONAL INSTITUTES OF HEALTH (United States)

f UNIVERSITY COLLEGE LONDON (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHILD; CHROMOSOME 7Q; DNA STRAND BREAKAGE; GENE LOCATION; GENE LOCUS; GENE MAPPING; GENE SEQUENCE; GENE TRANSLOCATION; GENETIC ANALYSIS; GENETIC MARKER; GENETIC RECOMBINATION; HUMAN; LANGUAGE DISABILITY; MALE; PRIORITY JOURNAL; SPEECH DISORDER;

EID: 0033865944 PISSN: 00029297 EISSN: None Source Type: Journal
DOI: 10.1086/303011 Document Type: Article

Times cited : (154)

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