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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 11, 2001
[Analysis of a case of balanced chromosome translocation and phenotypic abnormality by fluorescence in situ hybridization]G Zhu, O Bartsch, M Wan, et al.Human Genetics|October 1, 1994
Distinct RB1 gene mutations with low penetrance in hereditary retinoblastomaD R Lohmann, B Brandt, W Höpping, et al.Human Genetics|July 1, 1987
Detection of submicroscopic deletions and a DNA polymorphism at the retinoblastoma locusB Horsthemke, V Greger, H J Barnert, et al.Human Genetics|January 28, 1999
Mutations in the gene for the common gamma chain (gammac) in X-linked severe combined immunodeficiencyS D Fugmann, S Müller, W Friedrich, et al.British Journal of Haematology|December 1, 1988
Rapid and non-radioactive prenatal diagnosis of beta thalassaemia and sickle cell disease: application of the polymerase chain reaction (PCR)A E Kulozik, J Lyons, E Kohne, et al.European Journal of Pediatrics|May 1, 1995
Acute promyelocytic leukaemia with hypogranular bone marrow blasts in a 16-year-old girl: diagnostic value of different genetic methodsW Scherulen, J Harbott, J W Janssen, et al.Bone Marrow Transplantation|March 1, 1996
Graft-versus-host reaction spares normal stem cells in chronic myelogenous leukemiaH J Kolb, J Mittermüller, E Holler, et al.Leukemia|February 1, 1995
Improved detection of minimal residual leukemia through modifications of polymerase chain reaction analyses based on clonospecific T cell receptor junctionsT Seriu, T E Hansen-Hagge, D H Erz, et al.Journal of Medical Genetics|April 1, 1988
Application of linkage analysis to genetic counselling in families with hereditary retinoblastomaV Greger, S Kerst, E Messmer, et al.Journal of Medical Genetics|February 1, 1995
DNA methylation based testing of 450 patients suspected of having Prader-Willi syndromeG Gillessen-Kaesbach, S Gross, S Kaya-Westerloh, et al.Pageof 26