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Prenatal Diagnosis|November 1, 1992
Analysis of chromosome 21 copy number in uncultured amniocytes by fluorescence in situ hybridization using a cosmid contigY L Zheng, M A Ferguson-Smith, J P Warner, et al.Journal of Medical Genetics|October 1, 1992
A male with trisomy 9 mosaicism and maternal uniparental disomy for chromosome 9 in the euploid cell lineL R Willatt, B C Davison, D Goudie, et al.Prenatal Diagnosis|May 1, 1994
Second-trimester maternal serum screening using alpha-fetoprotein, human chorionic gonadotrophin, and unconjugated oestriol: experience of a regional programmeS F Goodburn, J R Yates, P R Raggatt, et al.Clinical Genetics|October 1, 1975
Prenatal diagnosis and family studies in a case of propionicacidaemiaD Gompertz, P A Goodey, H Thom, et al.Human Genetics|August 1, 1993
Physical mapping of chromosome 3p25-p26 by fluorescence in situ hybridisation (FISH)M E Phipps, E R Maher, N A Affara, et al.TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|July 15, 2017
QTL associated with resistance to cassava brown streak and cassava mosaic diseases in a bi-parental cross of two Tanzanian farmer varieties, Namikonga and AlbertE A Masumba, F Kapinga, G Mkamilo, et al.Plos One|August 17, 2021
Collection, genotyping and virus elimination of cassava landraces from Tanzania and documentation of farmer knowledgeM E Ferguson, S Tumwegamire, C Chidzanga, et al.Pageof 3