Discriminating power of localized three-dimensional facial morphology

American Journal of Human Genetics

Volumn 77, Issue 6, 2005, Pages 999-1010

  Hammond, Peter ^a   Hutton, Tim J ^a   Allanson, Judith E ^h   Buxton, Bernard ^b   Campbell, Linda E ^d   Clayton Smith, Jill ^g   Donnai, Dian ^g   Karmiloff Smith, Annette ^c   Metcalfe, Kay ^g   Murphy, Kieran C ^f   Patton, Michael ^e   Pober, Barbara ⁱ   Prescott, Katrina ^c   Scambler, Pete ^c   Shaw, Adam ^e   Smith, Ann C M ^j,k   Stevens, Angela F ^d   Temple, I Karen ^l   Hennekam, Raoul ^c   Tassabehji, May ^g  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

^d KING'S COLLEGE LONDON   (United Kingdom)

^e ST GEORGE'S UNIVERSITY OF LONDON   (United Kingdom)

^f ROYAL COLLEGE OF SURGEONS IN IRELAND   (Ireland)

^g UNIVERSITY OF MANCHESTER   (United Kingdom)

^h Regional Geriatric Program of Eastern Ontario   (Canada)

ⁱ BOSTON CHILDREN S HOSPITAL   (United States)

^j NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^k GEORGETOWN UNIVERSITY MEDICAL CENTER   (United States)

^l UNIVERSITY OF SOUTHAMPTON   (United Kingdom)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CHROMOSOME 22Q11 DELETION SYNDROME; CHROMOSOME DELETION; CLINICAL EXAMINATION; CLINICAL FEATURE; CONTROLLED STUDY; FACE DYSMORPHIA; FACE MALFORMATION; GENETIC MODEL; GENOTYPE; GENOTYPE PHENOTYPE CORRELATION; HUMAN; MAJOR CLINICAL STUDY; MOUTH MALFORMATION; NOONAN SYNDROME; NOSE MALFORMATION; ORBIT; PATTERN RECOGNITION; PRIORITY JOURNAL; SMITH MAGENIS SYNDROME; SYNDROME; WILLIAMS BEUREN SYNDROME;

EID: 28144433319     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/498396     Document Type: Article

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