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Human Genetics|June 1, 1987
Localization of the ornithine aminotransferase gene and related sequences on two human chromosomesV Ramesh, R Eddy, G A Bruns, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1990
The major human erythroid DNA-binding protein (GF-1): primary sequence and localization of the gene to the X chromosomeL I Zon, S F Tsai, S Burgess, et al.
Plos One|June 11, 2015
Effects of Row-Type, Row-Spacing, Seeding Rate, Soil-Type, and Cultivar Differences on Soybean Seed Nutrition under US Mississippi Delta ConditionsNacer Bellaloui, Herbert A Bruns, Hamed K Abbas, et al.
American Journal of Human Genetics|April 1, 1986
Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to chromosome 19L Bufton, G A Bruns, R E Magenis, et al.
The Journal of Experimental Medicine|May 1, 1985
T cell receptor alpha chain genes are located on chromosome 14 at 14q11-14q12 in humansN Caccia, G A Bruns, I R Kirsch, et al.
Environmental Science & Technology|July 9, 2010
Identification of organic nitrates in the NO3 radical initiated oxidation of alpha-pinene by atmospheric pressure chemical ionization mass spectrometryVéronique Perraud, Emily A Bruns, Michael J Ezell, et al.
Somatic Cell Genetics|March 1, 1978
Assignment of a Mus musculus gene for triosephosphate isomerase to chromosome 6 and for glyoxalase-I to chromosome 17 using somatic cell hybridsJ D Minna, G A Bruns, A H Krinsky, et al.
American Journal of Medical Genetics. Part A|January 5, 2023
Seizures in trisomy 18: Prevalence, description, and treatmentSue L Jaspersen, Deborah A Bruns, Meghan S Candee, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 9, 1995
Primary structure of hepatocyte nuclear factor/forkhead homologue 4 and characterization of gene expression in the developing respiratory and reproductive epitheliumB P Hackett, S L Brody, M Liang, et al.
Investigative Ophthalmology & Visual Science|August 11, 2000
X-linked retinitis pigmentosa: mutation spectrum of the RPGR and RP2 genes and correlation with visual functionD Sharon, G A Bruns, T L McGee, et al.
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