Genetics of human Bardet–Biedl syndrome, an updates
2016 · Clinical Genetics · 153 citations
https://doi.org/10.1111/cge.12737
S
Sher Alam Khan
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Sher Alam Khan is an academic researcher from Kohat University of Science and Technology. The author has contributed to research in topics: Wnt/β-catenin signaling in development and cancer & Skin and Cellular Biology Research & dental development and anomalies. The author has an h-index of 12, co-authored 42 publications.
ORCID: 0000-0001-5436-8917Papers by this author
worksGenetics of human Bardet–Biedl syndrome, an updates
2016 · Clinical Genetics · 153 citations
https://doi.org/10.1111/cge.12737
A novel mutation in the <i>HPGD</i> gene causing primary hypertrophic osteoarthropathy with digital clubbing in a Pakistani family
2017 · Annals of Human Genetics · 13 citations
https://doi.org/10.1111/ahg.12239
A novel nonsense variant in SLC24A4 causing a rare form of amelogenesis imperfecta in a Pakistani family
2020 · BMC Medical Genetics · 11 citations
https://doi.org/10.1186/s12881-020-01038-6
Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet–Biedl Syndrome
2023 · Genes · 10 citations
https://doi.org/10.3390/genes14051113
Novel Homozygous Mutations in the Genes TGM1, SULT2B1, SPINK5 and FLG in Four Families Underlying Congenital Ichthyosis
2021 · Genes · 9 citations
https://doi.org/10.3390/genes12030373
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