Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcription factor gene

Human Molecular Genetics

Volumn 8, Issue 4, 1999, Pages 625-637

  Hong, Hee Kyung ^a   Lass, Jonathan H ^b   Chakravarti, Aravinda ^a  

^a UNIVERSITY HOSPITALS OF CLEVELAND   (United States)

^b CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BIRTH DEFECT; CONGENITAL HYDROCEPHALUS; GENE ISOLATION; GENE MUTATION; GENETIC MARKER; GENETIC TRANSCRIPTION; HETEROZYGOTE; HOMOZYGOSITY; HOMOZYGOTE; MOUSE; MULTIGENE FAMILY; NEURAL CREST; NONHUMAN; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; PHENOTYPE; PLEIOTROPY; PRIORITY JOURNAL;

EID: 0033041178     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/8.4.625     Document Type: Article

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