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Van Keuren, M L; Stewart, G D; Bradley, C M et al. (1989) Characterization of an unusual and complex chromosome 21 rearrangement using somatic cell genetics and cloned DNA probes. Am J Med Genet 33:369-75
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Kurachi, S; Baldori, N; Kurnit, D M (1989) Sumo15A: a lambda phasmid that permits easy selection for and against cloned inserts. Gene 85:35-43
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Kurnit, D M (1989) Escherichia coli recA deletion strains that are highly competent for transformation and for in vivo phage packaging. Gene 82:313-5
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Tantravahi, U; Stewart, G D; Van Keuren, M et al. (1988) Isolation of DNA sequences on human chromosome 21 by application of a recombination-based assay to DNA from flow-sorted chromosomes. Hum Genet 79:196-202
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Stewart, G D; Hassold, T J; Berg, A et al. (1988) Trisomy 21 (Down syndrome): studying nondisjunction and meiotic recombination by using cytogenetic and molecular polymorphisms that span chromosome 21. Am J Hum Genet 42:227-36
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Stewart, G D; Hassold, T J; Kurnit, D M (1988) Trisomy 21. Molecular and cytogenetic studies of nondisjunction. Adv Hum Genet 17:99-140
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Tanzi, R E; Gusella, J F; Watkins, P C et al. (1987) Amyloid beta protein gene: cDNA, mRNA distribution, and genetic linkage near the Alzheimer locus. Science 235:880-4
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Neve, R L; Perrone-Bizzozero, N I; Finklestein, S et al. (1987) The neuronal growth-associated protein GAP-43 (B-50, F1): neuronal specificity, developmental regulation and regional distribution of the human and rat mRNAs. Brain Res 388:177-83
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Kurnit, D M; Layton, W M; Matthysse, S (1987) Genetics, chance, and morphogenesis. Am J Hum Genet 41:979-95
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Stewart, G D; Bruns, G A; Wasmuth, J J et al. (1987) An anonymous DNA segment (II227) maps to the long arm of human chromosome 5 and identifies a BstXI polymorphism (D5S26). Nucleic Acids Res 15:3939
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