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Saad Ullah Khan

Saad Ullah Khan

Kohat University of Science & Technology - Kohat / Pakistan
Natural Sciences / Molecular Biology & Genetics
AD Scientific Index ID: 517370
کوہاٹ یونیورسٹی سائنس اور ٹیکنالوجی
person_outline Saad Ullah Khan's MOST POPULAR ARTICLES
1-) Genetics of human Bardet–Biedl syndrome, an updates Clinical genetics 90 (1), 3-15, 2016
2-) Mutations in KARS, encoding lysyl-tRNA synthetase, cause autosomal-recessive nonsyndromic hearing impairment DFNB89 The American Journal of Human Genetics 93 (1), 132-140, 2013
3-) Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability Human genetics 137 (9), 735-752, 2018
4-) Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p Human genetics 130 (6), 759-765, 2011
5-) A novel homozygous missense mutation in WNT10B in familial split‐hand/foot malformation Clinical genetics 82 (1), 48-55, 2012