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American Journal of Medical Genetics|September 15, 1993
X-inactivation pattern in an Ullrich-Turner syndrome patient with a small ring X and normal intelligenceJ L Zenger-Hain, A Wiktor, J Goldman, et al.American Journal of Medical Genetics|December 1, 1993
Inverted duplication of chromosome 5p14p15.3 confirmed with in situ hybridizationJ L Zenger-Hain, D L Van Dyke, A Wiktor, et al.Annales De Genetique|November 6, 2001
Deletion of 2q37 and duplication of 10q24: two cases in the same family and review of the literatureA Wiktor, G L Feldman, E V Bawle, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 8, 2001
Prenatal diagnosis of 22q11.2 deletion when ultrasound examination reveals a heart defectS Manji, J R Roberson, A Wiktor, et al.Genes, Chromosomes & Cancer|November 24, 1999
Clinical significance of Y chromosome loss in hematologic diseaseA Wiktor, B A Rybicki, Z S Piao, et al.American Journal of Medical Genetics|August 1, 1992
Ullrich-Turner syndrome with a small ring X chromosome and presence of mental retardationD L Van Dyke, A Wiktor, C G Palmer, et al.American Journal of Medical Genetics|September 6, 1996
Toward quality assurance for metaphase FISH: a multi-center experienceG Dewald, R Stallard, P I Bader, et al.American Journal of Medical Genetics|April 17, 1998
A multicenter investigation with interphase fluorescence in situ hybridization using X- and Y-chromosome probesG Dewald, R Stallard, A Al Saadi, et al.American Journal of Medical Genetics|October 28, 1996
Toward quality assurance for metaphase FISH: a multicenter experienceG W Dewald, R Stallard, P I Bader, et al.Cancer Genetics and Cytogenetics|January 20, 2000
A multicenter investigation with D-FISH BCR/ABL1 probesG Dewald, R Stallard, A Alsaadi, et al.Pageof 2