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Nucleic Acids Research, ISSN 0305-1048, 01/2017, Volume 45, Issue 1, pp. D12 - D17
The National Center for Biotechnology Information (NCBI) provides a large suite of online resources for biological information and data, including the GenBank... 
Genome, Bacterial | National Library of Medicine (U.S.) | Sequence Alignment | Databases, Chemical | United States | Databases, Protein | Genomics | Systems Integration | Databases, Genetic | Drug Resistance, Microbial - genetics | PubMed | Database Issue
Journal Article
Nucleic Acids Research, ISSN 0305-1048, 2016, Volume 44, Issue 1, pp. D7 - D19
Journal Article
Nucleic Acids Research, ISSN 0305-1048, 01/2013, Volume 41, Issue 1, pp. D8 - D20
Journal Article
Nucleic Acids Research, ISSN 0305-1048, 01/2014, Volume 42, Issue 1, pp. D7 - D17
Journal Article
Nucleic Acids Research, ISSN 0305-1048, 01/2015, Volume 43, Issue 1, pp. D6 - D17
Journal Article
Nucleic Acids Research, ISSN 0305-1048, 1/2012, Volume 40, Issue D1, pp. D13 - D25
Journal Article
by Agarwala, Richa and Barrett, Tanya and Beck, Jeff and Benson, Dennis A and Bollin, Colleen and Bolton, Evan and Bourexis, Devon and Brister, J Rodney and Bryant, Stephen H and Canese, Kathi and Cavanaugh, Mark and Charowhas, Chad and Clark, Karen and Dondoshansky, Ilya and Feolo, Michael and Fitzpatrick, Lawrence and Funk, Kathryn and Geer, Lewis Y and Gorelenkov, Viatcheslav and Graeff, Alan and Hlavina, Wratko and Holmes, Brad and Johnson, Mark and Kattman, Brandi and Khotomlianski, Viatcheslav and Kimchi, Avi and Kimelman, Michael and Kimura, Masato and Kitts, Paul and Klimke, William and Kotliarov, Alex and Krasnov, Sergey and Kuznetsov, Anatoliy and Landrum, Melissa J and Landsman, David and Lathrop, Stacy and Lee, Jennifer M and Leubsdorf, Carl and Lu, Zhiyong and Madden, Thomas L and Marchler-Bauer, Aron and Malheiro, Adriana and Meric, Peter and Karsch-Mizrachi, Ilene and Mnev, Anatoly and Murphy, Terence and Orris, Rebecca and Ostell, James and O'Sullivan, Christopher and Palanigobu, Vasuki and Panchenko, Anna R and Phan, Lon and Pierov, Borys and Pruitt, Kim D and Rodarmer, Kurt and Sayers, Eric W and Schneider, Valerie and Schoch, Conrad L and Schuler, Gregory D and Sherry, Stephen T and Siyan, Karanjit and Soboleva, Alexandra and Soussov, Vladimir and Starchenko, Grigory and Tatusova, Tatiana A and Thibaud-Nissen, Francoise and Todorov, Kamen and Trawick, Bart W and Vakatov, Denis and Ward, Minghong and Yaschenko, Eugene and Zasypkin, Aleksandr and Zbicz, Kerry and NCBI Resource Coordinators
Nucleic Acids Research, ISSN 0305-1048, 01/2018, Volume 46, Issue D1, pp. D8 - D13
Abstract The National Center for Biotechnology Information (NCBI) provides a large suite of online resources for biological information and data, including the... 
BIOCHEMISTRY & MOLECULAR BIOLOGY | Database Issue
Journal Article
European Journal of Haematology, ISSN 0902-4441, 06/2017, Volume 98, Issue 6, p. 553
[alpha]-Thalassemia, one of the most common genetic diseases, is caused by deletions or point mutations affecting one to four [alpha]-globin genes. Molecular... 
Hemoglobin | Thalassemia | Algorithms | Diagnosis | Gene mutations | Analysis | Polymerase chain reaction | Laboratories | Anemia | Mutation
Journal Article
European Journal of Haematology, ISSN 0902-4441, 09/2018, Volume 101, Issue 3, pp. 297 - 304
Background Most patients with anemia are diagnosed through clinical phenotype and basic laboratory testing. Nonetheless, in cases of rare congenital anemias,... 
red cell disorders | DYSERYTHROPOIETIC ANEMIA | HEREDITARY STOMATOCYTOSIS | GENE | RECOMMENDATIONS | PIEZO1 | PYRUVATE-KINASE DEFICIENCY | SPLENECTOMY | MUTATIONS | HEMATOLOGY | BONE-MARROW FAILURE | NONSPHEROCYTIC HEMOLYTIC-ANEMIA | Genetic Testing | Anemia - blood | Anemia, Hemolytic, Congenital Nonspherocytic - diagnosis | Humans | Anemia, Dyserythropoietic, Congenital - diagnosis | Child, Preschool | Pyruvate Metabolism, Inborn Errors - genetics | Erythrocyte Indices | Male | Young Adult | Hydrops Fetalis - genetics | Anemia, Sideroblastic - diagnosis | Pyruvate Metabolism, Inborn Errors - diagnosis | Adult | Female | Child | Genetic Predisposition to Disease | Anemia, Dyserythropoietic, Congenital - therapy | Genetic Association Studies | Hydrops Fetalis - diagnosis | Anemia - diagnosis | Anemia, Dyserythropoietic, Congenital - genetics | Computational Biology | Anemia - therapy | Rare Diseases | Anemia, Hemolytic, Congenital - genetics | Pyruvate Kinase - deficiency | Anemia - congenital | Anemia, Sideroblastic - genetics | Anemia, Hemolytic, Congenital - diagnosis | Bone Marrow - pathology | Adolescent | High-Throughput Nucleotide Sequencing | Mutation | Pyruvate Kinase - genetics | Anemia, Hemolytic, Congenital Nonspherocytic - genetics | Anemia | Genetic disorders | Medical genetics | Phenotypes | Genetic counseling | Pyruvate kinase | Pyruvic acid | Sideroblastic anemia | Diagnosis | Kinases | Genetic screening
Journal Article