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Molecular Genetics and Metabolism|September 21, 2013
Undiagnosed phenylketonuria in parents of phenylketonuric patients, is it worthwhile to be checked?A Wiedemann, B Leheup, S-F Battaglia-Hsu, et al.Prenatal Diagnosis|February 17, 2001
Use of PRINS for preconception screening of polar bodies for common aneuploidiesC Petit, V Martel-Petit, A Fleurentin, et al.Genes, Chromosomes & Cancer|January 1, 1995
Inversion-associated translocations in acute myelomonocytic leukemia with eosinophiliaR Berger, J Derré, M Le Coniat, et al.Bioinformatics (Oxford, England)|December 2, 2008
Gene-disease relationship discovery based on model-driven data integration and database view definitionS Yilmaz, P Jonveaux, C Bicep, et al.Journal of Medical Genetics|July 1, 2009
Phenotypic variability in Rett syndrome associated with FOXG1 mutations in femalesC Philippe, D Amsallem, C Francannet, et al.Human Molecular Genetics|August 11, 1999
The signal transducer and activator of transcription STAT5b gene is a new partner of retinoic acid receptor alpha in acute promyelocytic-like leukaemiaC Arnould, C Philippe, V Bourdon, et al.Genes, Chromosomes & Cancer|January 1, 1996
Chromosome microdissection in leukemia: a powerful tool for the analysis of complex chromosomal rearrangementsP Jonveaux, M Le Coniat, J Derre, et al.Leukemia|September 1, 1995
Partial duplication of HRX in acute leukemia with trisomy 11O A Bernard, S P Romana, S A Schichman, et al.Prenatal Diagnosis|March 1, 2000
Dicentric marker derived from chromosome 22 associated with mild clinical signs: a case reportL Lohmann, N Chelloug, B Rosales, et al.British Journal of Haematology|May 1, 1995
Leukaemic non-Hodgkin's lymphomas with hyperdiploid cells and t(11;14)(q13;q32): a subtype of mantle cell lymphoma?M T Daniel, I Tigaud, M A Flexor, et al.Pageof 10