Literature DB >> 9882098

Coinheritance of alpha-and beta-spectrin gene mutations in a case of hereditary elliptocytosis.

D Dhermy, C Galand, O Bournier, M J King, T Cynober, I Roberts, F Kanyike, A Adekile.   

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Year:  1998        PMID： 9882098

Source DB:  PubMed          Journal:  Blood        ISSN： 0006-4971            Impact factor:   22.113


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  3 in total

1.  Genotype-phenotype correlations in hereditary elliptocytosis and hereditary pyropoikilocytosis.

Authors:  Omar Niss; Satheesh Chonat; Neha Dagaonkar; Marya O Almansoori; Karol Kerr; Zora R Rogers; Patrick T McGann; Maa-Ohui Quarmyne; Mary Risinger; Kejian Zhang; Theodosia A Kalfa
Journal:  Blood Cells Mol Dis       Date:  2016-07-17       Impact factor: 3.039

2.  Diagnostic tool for red blood cell membrane disorders: Assessment of a new generation ektacytometer.

Authors:  Lydie Da Costa; Ludovic Suner; Julie Galimand; Amandine Bonnel; Tiffany Pascreau; Nathalie Couque; Odile Fenneteau; Narla Mohandas
Journal:  Blood Cells Mol Dis       Date:  2015-09-16       Impact factor: 3.039

3.  Exome sequencing for diagnosis of congenital hemolytic anemia.

Authors:  Lamisse Mansour-Hendili; Abdelrazak Aissat; Bouchra Badaoui; Mehdi Sakka; Christine Gameiro; Valérie Ortonne; Orianne Wagner-Ballon; Serge Pissard; Véronique Picard; Khaldoun Ghazal; Michel Bahuau; Corinne Guitton; Ziad Mansour; Mylène Duplan; Arnaud Petit; Nathalie Costedoat-Chalumeau; Marc Michel; Pablo Bartolucci; Stéphane Moutereau; Benoît Funalot; Frédéric Galactéros
Journal:  Orphanet J Rare Dis       Date:  2020-07-08       Impact factor: 4.123
  3 in total

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