Cynthia Casson Morton, Ph.D.
This page shows the publications co-authored by Cynthia Morton and Jonathan Seidman.
Genes for beta chain of human T-cell antigen receptor map to regions of chromosomal rearrangement in T cells. Science. 1985 May 03; 228(4699):582-5.
Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction. Nat Genet. 1998 Nov; 20(3):299-303.
Regional localization of the human G protein alpha i2 (GNAI2) gene: assignment to 3p21 and a related sequence (GNAI2L) to 12p12-p13. Genomics. 1992 Jan; 12(1):125-9.
The gene for the alpha i1 subunit of human guanine nucleotide binding protein maps near the cystic fibrosis locus. Am J Hum Genet. 1988 Jun; 42(6):884-8.
Detection of a frequent restriction fragment length polymorphism in the human T cell antigen receptor beta chain locus. A potential diagnostic tool. J Clin Invest. 1985 Sep; 76(3):1283-5.
Human gamma-chain genes are rearranged in leukaemic T cells and map to the short arm of chromosome 7. Nature. 1985 Aug 8-14; 316(6028):549-52.
Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations. Proc Natl Acad Sci U S A. 1999 Mar 16; 96(6):2919-24.
Identification, characterization, and chromosomal localization of the human homolog (hES) of ES/130. Genomics. 1996 Aug 01; 35(3):628-31.
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