000 01760 a2200517 4500
005 20250516221633.0
264 0 _c20150219
008 201502s 0 0 eng d
022 _a1932-6203
024 7 _a10.1371/journal.pone.0100516
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aRumaney, Maryam Bibi
245 0 0 _aThe co-inheritance of alpha-thalassemia and sickle cell anemia is associated with better hematological indices and lower consultations rate in Cameroonian patients and could improve their survival.
_h[electronic resource]
260 _bPloS one
_c2014
300 _ae100516 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aAge Factors
650 0 4 _aAnemia, Sickle Cell
_xblood
650 0 4 _aBlood Cell Count
650 0 4 _aCameroon
650 0 4 _aFemale
650 0 4 _aGene Deletion
650 0 4 _aHaplotypes
650 0 4 _aHemoglobin A
_xgenetics
650 0 4 _aHemoglobin, Sickle
_xgenetics
650 0 4 _aHumans
650 0 4 _aInheritance Patterns
650 0 4 _aMale
650 0 4 _aMultigene Family
650 0 4 _aPolymorphism, Single Nucleotide
650 0 4 _aReferral and Consultation
_xstatistics & numerical data
650 0 4 _aSurvival Analysis
650 0 4 _aalpha-Globins
_xgenetics
650 0 4 _aalpha-Thalassemia
_xblood
650 0 4 _abeta-Globins
_xgenetics
700 1 _aNgo Bitoungui, Valentina Josiane
700 1 _aVorster, Anna Alvera
700 1 _aRamesar, Raj
700 1 _aKengne, Andre Pascal
700 1 _aNgogang, Jeanne
700 1 _aWonkam, Ambroise
773 0 _tPloS one
_gvol. 9
_gno. 6
_gp. e100516
856 4 0 _uhttps://doi.org/10.1371/journal.pone.0100516
_zAvailable from publisher's website
999 _c23965723
_d23965723