Search Results - "Al Balwi, M. A."

HLA-A, -B, -C, -DRB1 and -DQB1 allele and haplotype frequencies in Saudis using next generation sequencing technique by Hajeer, A. H., Al Balwi, M. A., Aytül Uyar, F., AlHaidan, Y., AlAbdulrahman, A., Al Abdulkareem, I., Al Jumah, M.

“…Next generation sequencing (NGS) is a promising technique that can reveal the entire gene sequences and to the highest possible resolution without any phase…”
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PRF1 gene mutation in a Saudi patient with haemophagocytic lymphohistiocytosis by Al Balwi, M. A., Al Harbi, T., Al Abdulkareem, I., Hajeer, A. H.

“…Haemophagocytic lymphohistiocytosis (HLH) is a rare autosomal inherited disease associated with activated macrophages that engulf erythrocytes, leucocytes,…”
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Congenital Duplication of the Palm Syndrome: Gene Analysis and the Molecular Basis of its Clinical Features by AL-QATTAN, M. M., AL-BALWI, M., EYAID, W., AL-ABDULKARIM, I., AL-TURKI, S.

“…Congenital duplication of the palm is a rare syndrome with the following features: the dorsal aspects of both hands have thick palmar skin with no hair or…”
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Association of SNPs rs6498169 and rs 10984447 with multiple sclerosis in Saudi patients: a model of the usefulness of familial aggregates in identifying genetic linkage in a multifactorial disease by AL JUMAH, M, AL BALWI, M, HUSSEIN, M, KOJAN, S, AL KHATHAAMI, A, AL FAWAZ, M, AL MUZAINI, B, JAWHARY, A, ALABDULKAREEM, I

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