The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; no phenotype prediction from the position of GLI3 mutations

American Journal of Human Genetics

Volumn 65, Issue 3, 1999, Pages 645-655

  Radhakrishna, Uppala ^a   Bornholdt, Dorothea ^c   Scott, Hamish S ^a   Patel, Uday C ^d   Rossier, Colette ^a   Engel, Hartmut ^c   Bottani, Armand ^b   Chandal, Divya ^e   Blouin, Jean Louis ^b   Solanki, Jitendra V ^d   Grzeschik, Karl Heinz ^c   Antonarakis, Stylianos E ^a,b,f  

^a UNIVERSITY OF GENEVA MEDICAL SCHOOL   (Switzerland)

^b University Hospital   (Germany)

^c PHILIPPS UNIVERSITY MARBURG   (Germany)

^d VETERINARY COLLEGE   (India)

^e GUJARAT UNIVERSITY   (India)

^f Centre Médical Universitaire   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; GENE MUTATION; GENETIC TRANSCRIPTION; HUMAN; HUMAN CELL; MULTIGENE FAMILY; NONSENSE MUTATION; PHENOTYPE; POLYDACTYLY; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN DOMAIN; PROTEIN LOCALIZATION; REGULATOR GENE; TRANSCRIPTION REGULATION;

EID: 0033362154     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302557     Document Type: Article

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