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Detection of non-deletional type of hereditary persistence of fetal hemoglobin (HPFH) condition associated with 619 bp β(°)-thalassemia deletion

DNA samples from a family (parents and a son) with hereditary persistence of fetal hemoglobin (HPFH) condition were subjected to amplification of a 1.214 kbp DNA fragment from β-globin gene using polymerase chain reaction (PCR). The aim of this study was to identify the type of HPFH i.e. deletional...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Husain, Syed Mazher, Anandaraj, M. P. J. S.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Springer India 1997
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC3453670/
https://ncbi.nlm.nih.gov/pubmed/23100882
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/BF02873679
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