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American Journal of Medical Genetics|September 1, 1988
Maternal serum alpha-fetoprotein screening for Down syndrome: economic considerationsJ M Swint, F GreenbergAmerican Journal of Medical Genetics|January 1, 1989
Mild Brachmann-de Lange syndrome: changes of phenotype with ageF Greenberg, L K RobinsonProceedings of the National Academy of Sciences of the United States of America|September 1, 1987
Isolation of anonymous DNA sequences from within a submicroscopic X chromosomal deletion in a patient with choroideremia, deafness, and mental retardationR L Nussbaum, J G Lesko, R A Lewis, et al.Human Genetics|June 1, 1991
Chromosomal assignment of a large tRNA gene cluster (tRNA(Leu), tRNA(Gln), tRNA(Lys), tRNA(Arg), tRNA(Gly)) to 17p13.1N Morrison, J P Goddard, D H Ledbetter, et al.The Journal of Pediatrics|May 1, 1993
Wilms tumor in a patient with Prader-Willi syndromeM J Coppes, H Sohl, I E Teshima, et al.Cytogenetics and Cell Genetics|January 1, 1980
Ring chromosome 15: phenotype, Ag-NOR analysis, secondary aneuploidy, and associated chromosome instabilityD H Ledbetter, V M Riccardi, W W Au, et al.American Journal of Human Genetics|April 1, 1990
Five polymorphic microsatellite VNTRs on the human X chromosomeJ A Luty, Z Guo, H F Willard, et al.American Journal of Human Genetics|February 1, 1989
New polymorphisms at the DXS98 locus and confirmation of its location proximal to FRAXA by in situ hybridizationR E Schnur, S A Ledbetter, D H Ledbetter, et al.Ophthalmology|December 1, 1988
The Williams syndrome. Spectrum and significance of ocular featuresF Greenberg, R A LewisPageof 33