Samuel A. Latt
Affiliations: | Harvard Medical School, Boston, MA, United States |
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Parents
Sign in to add mentor| Herbert Alexander Sober | grad student | National Cancer Institute | |
| Bert Lester Vallee | grad student | Harvard Medical School (Chemistry Tree) |
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| Bianchi DW, Flint AF, Pizzimenti MF, et al. (1990) Isolation of fetal DNA from nucleated erythrocytes in maternal blood. Proceedings of the National Academy of Sciences of the United States of America. 87: 3279-83 |
| Heartlein MW, Latt SA. (1989) Amplified inverted duplications within and adjacent to heterologous selectable DNA. Nucleic Acids Research. 17: 1697-716 |
| Rudolph NS, Latt SA. (1989) Flow cytometric analysis of X-ray sensitivity in ataxia telangiectasia Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis. 211: 31-41 |
| Rudolph NS, Nagasawa H, Little JB, et al. (1989) Identification of ataxia telangiectasia heterozygotes by flow cytometric analysis of X-ray damage Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis. 211: 19-29 |
| Tantravahi U, Nicholls RD, Stroh H, et al. (1989) Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndrome American Journal of Medical Genetics. 33: 78-87 |
| Simon M, Phillips M, Green H, et al. (1989) Absence of a single repeat from the coding region of the human involucrin gene leading to RFLP. American Journal of Human Genetics. 45: 910-6 |
| Nicholls RD, Knoll JH, Glatt K, et al. (1989) Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome. American Journal of Medical Genetics. 33: 66-77 |
| Knoll JH, Nicholls RD, Magenis RE, et al. (1989) Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion. American Journal of Medical Genetics. 32: 285-90 |
| Tantravahi U, Stewart GD, 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. Human Genetics. 79: 196-202 |
| Heartlein MW, Knoll JH, Latt SA. (1988) Chromosome instability associated with human alphoid DNA transfected into the Chinese hamster genome. Molecular and Cellular Biology. 8: 3611-8 |