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Molecular and Cellular Biology|May 1, 1993
Functional analysis of a stable transcription arrest site in the first intron of the murine adenosine deaminase geneS F Kash, J W Innis, A U Jackson, et al.Molecular and Cellular Biology|December 1, 1991
Sequence requirements for transcriptional arrest in exon 1 of the human adenosine deaminase geneZ Chen, J W Innis, M H Sun, et al.Molecular and Cellular Biology|January 1, 1985
Role of specific simian virus 40 sequences in the nuclease-sensitive structure in viral chromatinR D Gerard, B A Montelone, C F Walter, et al.The Journal of Biological Chemistry|November 15, 1991
The murine adenosine deaminase promoter requires an atypical TATA box which binds transcription factor IID and transcriptional activity is stimulated by multiple upstream Sp1 binding sitesJ W Innis, D J Moore, S F Kash, et al.The Laryngoscope|August 1, 1996
Familial large vestibular aqueduct syndromeA J Griffith, A Arts, C Downs, et al.American Journal of Human Genetics|January 1, 1996
Characterization of 12 silent alleles of the human butyrylcholinesterase (BCHE) geneS L Primo-Parmo, C F Bartels, B Wiersema, et al.American Journal of Medical Genetics|August 22, 1997
Exclusion of BMP6 as a candidate gene for cleidocranial dysplasiaJ W Innis, J H Asher, Y Liang, et al.American Journal of Human Genetics|June 7, 2000
Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndromeF R Goodman, C Bacchelli, A F Brady, et al.American Journal of Human Genetics|March 21, 2000
Familial syndromic esophageal atresia maps to 2p23-p24J Celli, E van Beusekom, R C Hennekam, et al.Journal of Medical Genetics|April 18, 2009
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcomeB W M van Bon, H C Mefford, B Menten, et al.Pageof 3