Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome

Human Molecular Genetics

Volumn 8, Issue 9, 1999, Pages 1769-1777

  Kalff Suske, Martha ^a   Wild, Anja ^a   Topp, Juliane ^a   Wessling, Martina ^a   Jacobsen, Eva Maria ^a   Bornholdt, Dorothea ^a   Engel, Hartmut ^a   Heuer, Heike ^a   Aalfs, Cora M ^b   Ausems, Margreet G E M ^c   Barone, Rita ^d   Herzog, Andreas ⁿ   Heutink, Peter ^e   Homfray, Tessa ^f   Gillessen Kaesbach, Gabriele ^g   König, Rainer ^h   Kunze, Jürgen ⁱ   Meinecke, Peter ^j   Müller, Dietmar ^k   Rizzo, Renata ^d   Strenge, Sibylle ^l   Superti Furga, Andrea ^m   Grzeschik, Karl Heinz ^a   more..

^a PHILIPPS UNIVERSITY MARBURG   (Germany)

^b ACADEMIC MEDICAL CENTER   (Netherlands)

^c Klinisch Genetisch Centrum Utrecht   (Netherlands)

^d UNIVERSITY OF CATANIA   (Italy)

^e ERASMUS UNIVERSITY ROTTERDAM   (Netherlands)

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

^g UNIVERSITY HOSPITAL ESSEN   (Germany)

^h GOETHE UNIVERSITY   (Germany)

ⁱ HUMBOLDT UNIVERSITY   (Germany)

^j Altonaer Kinderkrankenhaus   (Germany)

^k KLINIKUM CHEMNITZ   (Germany)

^l UNIVERSITY OF LEIPZIG   (Germany)

^m Universitats Kinderklinik   (Switzerland)

ⁿ NONE

more..

Author keywords

[No Author keywords available]

Indexed keywords

DNA BINDING PROTEIN; ZINC FINGER PROTEIN;

AMINO TERMINAL SEQUENCE; ARTICLE; CARBOXY TERMINAL SEQUENCE; CRANIOFACIAL MALFORMATION; DEVELOPMENTAL GENETICS; LIMB MALFORMATION; MISSENSE MUTATION; PALLISTER HALL SYNDROME; PHENOTYPE; POINT MUTATION; POLYDACTYLY; PRIORITY JOURNAL; RNA SPLICING; SYNDACTYLY; TRANSACTIVATION;

ANIMALS; CRANIOFACIAL ABNORMALITIES; DNA MUTATIONAL ANALYSIS; DNA-BINDING PROTEINS; DROSOPHILA; HUMANS; KRUPPEL-LIKE TRANSCRIPTION FACTORS; LIMB DEFORMITIES, CONGENITAL; MUTATION; NERVE TISSUE PROTEINS; RECOMBINANT FUSION PROTEINS; REPRESSOR PROTEINS; SEQUENCE DELETION; SYNDROME; TRANS-ACTIVATION (GENETICS); TRANSCRIPTION FACTORS; TRANSFECTION; TUMOR CELLS, CULTURED; XENOPUS PROTEINS; ZINC FINGERS;

EID: 0032833002     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/8.9.1769     Document Type: Article

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