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Thrombosis and Haemostasis|November 1, 2000
Ethnic heterogeneity of the factor XIII Val34Leu polymorphismF A Attié-Castro, M A Zago, J Lavinha, et al.
Molecular Genetics and Metabolism|February 13, 2001
Molecular and structural analysis of two novel mutations in a patient with mut(-) methylmalonyl-CoA deficiencyJ F Benoist, C Acquaviva, I Callebaut, et al.
Human Genetics|September 1, 1991
Nucleotide sequence evidence of the unicentric origin of the beta C mutation in AfricaG Trabuchet, J Elion, O Dunda, et al.
European Journal of Human Genetics : EJHG|August 31, 2001
N219Y, a new frequent mutation among mut(degree) forms of methylmalonic acidemia in Caucasian patientsC Acquaviva, J F Benoist, I Callebaut, et al.
European Journal of Medical Genetics|May 21, 2009
Chromosome 22q13.3 deletion syndrome with a de novo interstitial 22q13.3 cryptic deletion disrupting SHANK3A Delahaye, A Toutain, A Aboura, et al.
Journal of Clinical Microbiology|July 1, 1991
DNA restriction fragment length polymorphism differentiates crossed from independent infections in nosocomial Xanthomonas maltophilia bacteremiaE H Bingen, E Denamur, N Y Lambert-Zechovsky, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 27, 2000
[Constitutional deficiency of pulmonary surfactant protein B: clinical presentation, histologic and molecular diagnosis]M Tredano, F Cneude, E Denamur, et al.
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