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91. Association of variants in PTPN22, CTLA‐4, IL2‐RA, and INS genes with type 1 diabetes in Emiratis. (24th September 2020)

95. Associations of the melanocortin 3 receptor C17A + G241A haplotype with body composition and inflammation in African‐American adults. (2nd April 2019)

98. Autosomal Dominant Hearing Loss resulting from p.R75Q Mutation in the GJB2 Gene: Nonsyndromic presentation in a South Indian Family. (13th November 2014)

100. BBS5 and INPP5E mutations associated with ciliopathy disorders in families from Pakistan. (7th June 2019)