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Prenatal Diagnosis|October 30, 1998
Prenatal diagnosis of congenital alveolar proteinosis (surfactant protein B deficiency)M Stuhrmann, B Bohnhorst, U Peters, et al.Public Health Genomics|March 6, 2010
Genetic screening in EuropeP Javaher, E Nyoungui, H Kääriäinen, et al.Nucleic Acids Research|November 11, 1987
A human Y-chromosomal DNA sequence expressed in testicular tissueJ Arnemann, J T Epplen, H J Cooke, et al.EXS|January 1, 1993
Oligonucleotide fingerprinting of free-ranging and captive rhesus macaques from Cayo Santiago: paternity assignment and comparison of heterozygosityP Nürnberg, J D Berard, F Bercovitch, et al.The Journal of Clinical Investigation|April 1, 1994
A novel exon in the cystic fibrosis transmembrane conductance regulator gene activated by the nonsense mutation E92X in airway epithelial cells of patients with cystic fibrosisK Will, T Dörk, M Stuhrmann, et al.Cytogenetics and Cell Genetics|February 15, 2001
TSPY variants in six loci on the human Y chromosomeF Dechend, G Williams, B Skawran, et al.Human Mutation|January 1, 1995
Somatic spectrum of cancer-associated single basepair substitutions in the TP53 gene is determined mainly by endogenous mechanisms of mutation and by selectionM Krawczak, B Smith-Sorensen, J Schmidtke, et al.Dalton Transactions (Cambridge, England : 2003)|July 15, 2004
Pyridylpyrrolides as alternatives to cyclometalated phenylpyridine ligands: synthesis and characterization of luminescent zinc and boron pyridylpyrrolide complexesJamie J Klappa, Sarah A Geers, Sarah J Schmidtke, et al.Saudi Medical Journal|September 21, 2016
The potential benefits of genetic testing in breast and ovarian cancerel-H A ElHarith, M S Abdel-Hadi, T Doerk, et al.Human Genetics|January 1, 1984
Restriction fragment length polymorphisms at the human parathyroid hormone gene locusJ Schmidtke, B Pape, U Krengel, et al.Pageof 25