Analysis of Hemochromatosis Gene Mutations in 52 Consecutive Patients with Polycythemia Vera

By Franchini Massimo   de Matteis Giovanna   Federici Francesca   Solero Pietro   Veneri Dino  

Hematology, Vol. 9, Iss. 5-6, 2004-10 ,pp. : 413-414

Maney Publishing

Access to resources Recommend Favorite

Genetic analysis in nine unrelated Italian patients affected by OTC deficiency: detection of novel mutations in the OTC gene

By Bisanzi S.   Morrone A.   Donati M.A.   Pasquini E.   Spada M.   Strisciuglio P.   Parenti G.   Parini R.   Papadia F.   Zammarchi E.  

Molecular Genetics and Metabolism, Vol. 76, Iss. 2, 2002-06 ,pp. : 137-144

Academic Press

Access to resources Recommend Favorite

Ankyrin gene mutations in japanese patients with hereditary spherocytosis

By Nakanishi Hidekazu   Kanzaki Akio   Yawata Ayumi   Yamada Osamu   Yawata Yoshihito  

International Journal of Hematology, Vol. 73, Iss. 1, 2001-01 ,pp. : 54-63

Springer Publishing Company

Access to resources Recommend Favorite

Self-Learning Fuzzy Control with Temporal Knowledge for Atracurium-Induced Neuromuscular Block during Surgery

By Mason D.G.   Ross J.J.   Edwards N.D.   Linkens D.A.   Reilly C.S.  

Computers and Biomedical Research, Vol. 32, Iss. 3, 1999-06 ,pp. : 187-197

Academic Press

Access to resources Recommend Favorite

Clinical heterogeneity and molecular findings in five Polish patients with glycerol kinase deficiency: investigation of two splice site mutations with computerized splice junction analysis and Xp21 gene-specific mRNA analysis

By Hellerud C.   Adamowicz M.   Jurkiewicz D.   Taybert J.   Kubalska J.   Ciara E.   Popowska E.   Ellis J.R.   Lindstedt S.   Pronicka E.  

Molecular Genetics and Metabolism, Vol. 79, Iss. 3, 2003-07 ,pp. : 149-159

Elsevier

Access to resources Recommend Favorite