Elucidating the spectrum of alpha thalassemia mutations in iran successful online dating profile for men
Conclusion: Knowing the alpha-genotype is helpful for genetic counseling, microcytic anemia discrimination and hemoglobinopathy prevention. The β-thalassemia syndromes, Blackwell Scientific publication: Oxford, 2001. World distribution, population genetics, and health burden of the hemoglobinopathies.
doi: 10.1111/j.1365-2141.2008.07085.x Higgs DR, Weatherall DJ. doi: 10.1007/s00018-008-8529-9 Harteveld CL, Higgs DR.
Cellular and molecular life sciences : CMLS 2009; 66(7): 1154-1162.
ICSH recommendations for the measurement of haemoglobin A2.
Accepting the NEJM cookie is necessary to use the website.
Our review of the molecular basis of β-thalassemia in various Arab countries…
The Arab countries encompass a wide region stretching from the Persian Gulf to the Atlantic Ocean.
However, no specific mutation is confined to the Arabs, although some Arab countries do have unique mutations. doi: 10.1186/1750-1172-5-13 Stephens AD, Angastiniotis M, Baysal E, et al. doi: 10.1111/j.1751-553X.2011.01368.x Sambrook J, Russell DW. Molecular Cloning: A Laboratory Manual, 3rd edn Cold Spring Harbor: Cold Spring Harbor Laboratory, 2001. Rapid detection of alpha-thalassaemia deletions and alpha-globin gene triplication by multiplex polymerase chain reactions. Hemoglobinopathies in newborns from Salvador, Bahia, Northeast Brazil. Adorno EV, Couto FD, Moura Neto JP, Menezes JF, Rego M, Reis MG et al. Alpha-thalassemia (3.7 kb deletion) in a population from the Brazilian Amazon region: Santarem, Para State. Please set your browser to accept cookies to continue.This cookie stores just a session ID; no other information is captured.