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Developmental Medicine and Child Neurology|June 1, 1980
Deficits in space-form perception in patients with sex chromosome mosaicism (45,X/46,XY)A J Ebbin, V V Howell, M G WilsonClinical Genetics|July 1, 1977
Chromosomal anomalies in patients with retinoblastomaM G Wilson, A J Ebbin, J W Towner, et al.Birth Defects Original Article Series|January 1, 1975
Sex chromosome mosaicism of X/XY or X/XY/XYYM G Wilson, A J Ebbin, N W Shinno, et al.Human Genetics|January 1, 1981
Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del(4p)]M G Wilson, J W Towner, G S Coffin, et al.Humangenetik|January 1, 1975
Familial inversion of chromosome No. 8: an affected child and a carrier fetusA Fujimoto, M G Wilson, J W TownerHuman Genetics|January 1, 1983
Duplication of the segment q12.2 leads to qter of chromosome 22 due to paternal inversion 22(p13q12.2)A Fujimoto, M G Wilson, J W TownerHuman Genetics|May 1, 1988
DA/DAPI-fluorescent heteromorphism of human Y chromosomeM S Lin, A Zhang, M G Wilson, et al.Cytogenetics and Cell Genetics|January 1, 1989
Sister chromatid exchanges in the human active and inactive X chromosomesA Zhang, M S Lin, M G Wilson, et al.Human Heredity|January 1, 1994
A rare 6q11+ heteromorphism: cytogenetic analysis and in situ hybridizationM S Lin, A Zhang, A Fujimoto, et al.Pageof 46