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Molecular and Cellular Probes|August 1, 1993
The parental origin of hydatidiform moles and blighted ova: molecular probing with hypervariable DNA polymorphismsE Trabetti, R Galavotti, L Zanini, et al.Bone Marrow Transplantation|September 1, 1992
Host origin of bone marrow fibroblasts following allogeneic bone marrow transplantation for chronic myeloid leukemiaM A Santucci, E Trabetti, G Martinelli, et al.Human Heredity|January 1, 1991
Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphismsP Gasparini, P Mandich, G Novelli, et al.Human Genetics|June 1, 1994
A base substitution at IVS-19 3'-end splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfectaM Mottes, A Sangalli, M Valli, et al.Journal of Medical Genetics|May 1, 1993
Molecular genetic diagnosis of autosomal dominant polycystic kidney disease in a newborn with bilateral cystic kidneys detected prenatally and multiple skeletal malformationsA E Turco, E M Padovani, G P Chiaffoni, et al.The European Respiratory Journal|March 29, 2003
Tumour necrosis factor family genes in a phenotype of COPD associated with emphysemaI Ferrarotti, M Zorzetto, M Beccaria, et al.Haematologica|March 1, 1991
Different suppression of Ph1 positive hemopoiesis induced by intensive chemotherapy in lymphoid and myeloid blast crisis of CMLA Guerrasio, G Martinelli, A Ambrosetti, et al.Journal of Molecular Evolution|December 1, 1995
Recurrent simple tandem repeat mutations during human Y-chromosome radiation in Caucasian subpopulationsB M Ciminelli, F Pompei, P Malaspina, et al.Clinical Pharmacology and Therapeutics|December 31, 2015
Incorporating patient preferences into drug development and regulatory decision making: Results from a quantitative pilot study with cancer patients, carers, and regulatorsD Postmus, M Mavris, H L Hillege, et al.Molecular and Cellular Probes|June 17, 1999
Two novel missense mutations causing adrenoleukodystrophy in Italian patientsC Perusi, M Gomez-Lira, M Mottes, et al.Pageof 15