Showing results (431-440 of 1,544) with videos related to

Sort By:
Pageof 155
British Journal of Haematology|September 24, 2004
Different impacts of alleles alphaLEPRA and alphaLELY as assessed versus a novel, virtually null allele of the SPTA1 gene in transJ Delaunay, V Nouyrigat, A Proust, et al.
British Journal of Haematology|March 1, 1997
Frequent de novo mutations of the ANK1 gene mimic a recessive mode of transmission in hereditary spherocytosis: three new ANK1 variants: ankyrins Bari, Napoli II and AnzioJ Randon, E Miraglia del Giudice, M Bozon, et al.
Prenatal Diagnosis|January 12, 2002
Dehydrated hereditary stomatocytosis: a cause of prenatal ascitesS Grootenboer, C Barro, T Cynober, et al.
Biochemistry|July 31, 1990
Structure and function of hemoglobin variants at an internal hydrophobic site: consequences of mutations at the beta 27 (B9) positionY Huang, J Pagnier, P Magne, et al.
Human Genetics|July 1, 1992
Alpha I/65 hereditary elliptocytosis in southern Italy: evidence for an African originE M del Giudice, M T Ducluzeau, N Alloisio, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 17, 2008
[Hereditary spherocytosis: guidelines for the diagnosis and management in children]C Guitton, L Garçon, T Cynober, et al.
Blood Cells, Molecules & Diseases|January 8, 2011
A genomic deletion causes truncation of α-spectrin and ellipto-poikilocytosisA Iolascon, M-J King, S Robertson, et al.
Blood|April 1, 1988
Spectrin Oran (alpha II/21), a new spectrin variant concerning the alpha II domain and causing severe elliptocytosis in the homozygous stateN Alloisio, L Morlé, B Pothier, et al.
British Journal of Haematology|May 1, 1991
Occurrence of the alpha I 22 Arg----His (CGT----CAT) spectrin mutation in Tunisia: potential association with severe elliptopoikilocytosisF Baklouti, J Marechal, L Morle, et al.
The Journal of Pharmacology and Experimental Therapeutics|September 19, 2001
Capsaicin inhibits Jurkat T-cell activation by blocking calcium entry current I(CRAC)B S Fischer, D Qin, K Kim, et al.
Pageof 155