Associated Papers
Whole genome mapping and identification of single nucleotide polymorphisms of four Bangladeshi individuals and their functional significance.
Khan S et al.
Bmc Research Notes, 2021
33743798 (PubMed )
Supplement: 13104_2021_5514_MOESM4_ESM.zip › Supplementary_File_1A-1.xlsx › Supplementary_File_1A-1.exonic_
Mutation detection in candidate genes for benign familial infantile seizures on a novel locus.
Li N et al.
The International Journal of Neuroscience, 2010
A common nonsense mutation in EphB2 is associated with prostate cancer risk in African American men with a positive family history.
Kittles RA et al.
Journal of Medical Genetics, 2006
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