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Cytogenetics and Cell Genetics|January 1, 1988
Pachytene analysis in males heterozygous for a familial translocation (9;12;13) (q22; q22; q32) ascertained through a child with partial trisomy 9R Johannisson, U Löhrs, E PassargeBirth Defects Original Article Series|June 1, 1971
Possible genetic heterogeneity of X-linked ichthyosisE Passarge, B Post, E SchöpfBlood|October 1, 1987
Analyses of phenotype and genotype in acute lymphoblastic leukemias at first presentation and in relapseA Raghavachar, E Thiel, C R BartramCytogenetics and Cell Genetics|January 1, 1987
Mapping of the oncogenes Myc, Sis, and int-1 to the distal part of mouse chromosome 15S Adolph, C R Bartram, H HameisterBlut|April 1, 1986
Biallelic heavy chain immunoglobulin gene rearrangement in acute nonlymphocytic leukemiaC R Bartram, A Raghavachar, H HeimpelBlood|April 15, 1990
Isochromosome 17q in Ph1-negative leukemia: a clinical, cytogenetic, and molecular studyR Becher, F Carbonell, C R BartramCancer Research|July 1, 1988
Immunoglobulin and T-cell receptor gene rearrangements in Hodgkin's diseaseA Raghavachar, T Binder, C R BartramDeutsche Medizinische Wochenschrift (1946)|April 1, 1976
[Cytogenetic and clinical findings in suspected Turner's syndrome: results of a five-year study of 207 patients (author's transl)]R Berghoff, R A Rüdiger, E PassargeTeratology|April 1, 1982
Fetal manifestation of a chromosomal disorder: partial duplication of the long arm of chromosome 5 (5q33 to qter)E Passarge, M Bartsch-Sandhoff, H RehderBirth Defects Original Article Series|June 1, 1971
Syndrome of cystic eyelids, palmo-plantar keratosis, hypodontia and hypotrichosis as a possible autosomal recessive traitE Schöpf, H J Schulz, E PassargePageof 26