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• A human Hox 1 homeobox gene exhibits myeloid-specific expression of alternative transcripts in human hematopoietic cells.

  Lowney P, Corral J, Detmer K, LeBeau MM, Deaven L, Lawrence HJ, Largman C. Lowney P, et al. Nucleic Acids Res. 1991 Jun 25;19(12):3443-9. doi: 10.1093/nar/19.12.3443. Nucleic Acids Res. 1991. PMID: 1676505 Free PMC article.
• Haplotyping the human T-cell receptor beta-chain gene complex by use of restriction fragment length polymorphisms.

  Charmley P, Chao A, Concannon P, Hood L, Gatti RA. Charmley P, et al. Proc Natl Acad Sci U S A. 1990 Jun;87(12):4823-7. doi: 10.1073/pnas.87.12.4823. Proc Natl Acad Sci U S A. 1990. PMID: 1972281 Free PMC article.
• No evidence for genetic linkage of Gilles de la Tourette syndrome on chromosomes 7 and 18.

  Heutink P, van de Wetering BJ, Breedveld GJ, Weber J, Sandkuyl LA, Devor EJ, Heiberg A, Niermeijer MF, Oostra BA. Heutink P, et al. J Med Genet. 1990 Jul;27(7):433-6. doi: 10.1136/jmg.27.7.433. J Med Genet. 1990. PMID: 2395161 Free PMC article.
• Molecular cytogenetic analysis of a familial 8p23.1 deletion associated with minimal dysmorphic features, seizures, and mild mental retardation.

  Pettenati MJ, Rao N, Johnson C, Hayworth R, Crandall K, Huff O, Thomas IT. Pettenati MJ, et al. Hum Genet. 1992 Aug;89(6):602-6. doi: 10.1007/BF00221946. Hum Genet. 1992. PMID: 1511976 Review.
• Evidence for the evolutionary origin of human chromosome 21 from comparative gene mapping in the cow and mouse.

  Threadgill DS, Kraus JP, Krawetz SA, Womack JE. Threadgill DS, et al. Proc Natl Acad Sci U S A. 1991 Jan 1;88(1):154-8. doi: 10.1073/pnas.88.1.154. Proc Natl Acad Sci U S A. 1991. PMID: 1986361 Free PMC article.