GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome

Nature Genetics

Volumn 15, Issue 3, 1997, Pages 266-268

  Kang, Seongman ^a   Graham Jr , John M ^b   Olney, Ann Haskins ^c   Biesecker, Leslie G ^a  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c UNIVERSITY OF NEBRASKA MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR; ZINC FINGER PROTEIN;

ARTICLE; BRAIN TUMOR; CHROMOSOME 7P; CLINICAL FEATURE; FRAMESHIFT MUTATION; HAMARTOMA; HUMAN; MALFORMATION SYNDROME; PALLISTER HALL SYNDROME; PEDIGREE ANALYSIS; POLYDACTYLY; PRIORITY JOURNAL; PROTEIN DOMAIN;

ABNORMALITIES, MULTIPLE; AMINO ACID SEQUENCE; BASE SEQUENCE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 7; DNA-BINDING PROTEINS; FEMALE; FRAMESHIFT MUTATION; HAMARTOMA; HUMANS; HYPOTHALAMIC DISEASES; INFANT, NEWBORN; KRUPPEL-LIKE TRANSCRIPTION FACTORS; MALE; MOLECULAR SEQUENCE DATA; NERVE TISSUE PROTEINS; PEDIGREE; POLYDACTYLY; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; REPRESSOR PROTEINS; SYNDROME; TRANSCRIPTION FACTORS; XENOPUS PROTEINS; ZINC FINGERS;

GENETTA; VERTEBRATA;

EID: 0031019090     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0397-266     Document Type: Article

References (19)

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