Mutation analysis anti embryonic expression of the HLXB9 currarino syndrome gene

American Journal of Human Genetics

Volumn 66, Issue 5, 2000, Pages 1504-1515

  Hagan, D M ^a   Ross, A J ^a   Strachan, T ^a,q   Lynch, S A ^a   Ruiz Perez, V ^a   Wang, Y M ^a   Scambler, P ^b   Custard, E ^b   Reardon, W ^b   Hassan, S ^b   Muenke, M ^f   Nixon, P ^b   Papapetrou, C ^b   Winter, R M ^b   Edwards, Y ^c   Morrison, K ^c   Barrow, M ^g   Cordier Alex, M P ^h   Correia, P ⁱ   Galvin Parton, P A ^j   Gaskill, S ^k   Gaskin, K J ^l   Garcia Minaur, S ^m   Gereige, R ⁿ   Hayward, R ^d   Homfray, T ^e   McKeown, C ^o   Murday, V ^e   Plauchu, H ^h   Shannon, N ^p   Spitz, L ^d   Lindsay, S ^a,q   more..

^a NEWCASTLE UNIVERSITY   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

^d GREAT ORMOND STREET HOSPITAL   (United Kingdom)

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

^f NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^g LEICESTER ROYAL INFIRMARY   (United Kingdom)

^h HÔTEL DIEU   (France)

ⁱ INSTITUTO OSWALDO CRUZ   (Brazil)

^j STONY BROOK UNIVERSITY   (United States)

^k Roy Alexandra Hosp for Sick C ^*  (United States)

^l CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

^m HOSPITAL DE CRUCES   (Spain)

ⁿ JOHNS HOPKINS ALL CHILDREN S HOSPITAL   (United States)

^o BIRMINGHAM WOMEN S HOSPITAL   (United Kingdom)

^p Centre for Human Genetics   (United Kingdom)

^q School of Biochemistry and Genetics   (United Kingdom)

more..

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID SUBSTITUTION; ANORECTAL MALFORMATION; ARTICLE; CLINICAL ARTICLE; DEVELOPMENTAL DISORDER; GENE EXPRESSION; GENE MAPPING; GENE MUTATION; GENETIC HETEROGENEITY; GENETIC SCREENING; GENOTYPE; HOMEOBOX; HUMAN; LANGUAGE DEVELOPMENT; MISSENSE MUTATION; MOSAICISM; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; TISSUE DISTRIBUTION; AMINO ACID SEQUENCE; ANIMAL; CHEMISTRY; CONGENITAL MALFORMATION; EMBRYO; GENE DELETION; GENETICS; GROWTH DISORDER; MALE; METABOLISM; MOLECULAR GENETICS; MOUSE; MULTIPLE MALFORMATION SYNDROME; MUTATION; NUCLEOTIDE SEQUENCE; SACRUM; STOP CODON; SYNDROME; TIME;

HOMEODOMAIN PROTEIN; MICROSATELLITE DNA;

ABNORMALITIES, MULTIPLE; AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ANIMALS; CODON, TERMINATOR; CONSERVED SEQUENCE; DNA MUTATIONAL ANALYSIS; EMBRYO; GENES, HOMEOBOX; GROWTH DISORDERS; HOMEODOMAIN PROTEINS; HUMANS; MALE; MICE; MICROSATELLITE REPEATS; MOLECULAR SEQUENCE DATA; MUTATION; MUTATION, MISSENSE; PHENOTYPE; SACRUM; SEQUENCE DELETION; SYNDROME; TIME FACTORS;

EID: 0033625433     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302899     Document Type: Article

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