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Association between oral cleft and transcobalamin 2 polymorphism in a sample study from Nassiriya, Iraq

Orofacial clefts are common congenital defects whose prevalence differs between geographical regions and ethnic groups. The inheritance is complex, involving the contribution of both genetic and environmental factors. The involvement of genes belonging to the folate pathway is still matter of debate...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Τόπος έκδοσης:Int J Immunopathol Pharmacol
Κύριοι συγγραφείς: Carinci, Francesco, Palmieri, Annalisa, Scapoli, Luca, Cura, Francesca, Abenavoli, Fabio, Giannì, Aldo Bruno, Russillo, Antonio, Docimo, Raffaella, Martinelli, Marcella
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: SAGE Publications 2019
Θέματα:
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6822189/
https://ncbi.nlm.nih.gov/pubmed/31663440
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2058738419855571
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