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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.Annales De Genetique|April 24, 1999
[Promiscuous genes and chromosomal rearrangements of hematopoietic malignancies]R BergerThe International Journal of Applied Radiation and Isotopes|December 1, 1982
Radical scavengers and the stability of 99mTc-radiopharmaceuticalsR BergerCancer Genetics and Cytogenetics|March 1, 1997
Acute lymphoblastic leukemia and chromosome 21R BergerPrenatal Diagnosis|February 17, 2001
Use of PRINS for preconception screening of polar bodies for common aneuploidiesC Petit, V Martel-Petit, A Fleurentin, 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.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.The American Journal of Managed Care|July 19, 2011
Functional improvement and symptom management in multiple sclerosis: clinical efficacy of current therapiesJoseph R BergerPageof 176