受强制性开放获取政策约束的文章 - Raja ali了解详情
无法在其他位置公开访问的文章：1 篇
Novel mutations in the gene HOXC13 underlying pure hair and nail ectodermal dysplasia in consanguineous families
RH Ali, R Habib, N Ud‐Din, MN Khan, M Ansar, W Ahmad
British Journal of Dermatology 169 (2), 478-480, 2013
强制性开放获取政策： German Research Foundation
可在其他位置公开访问的文章：6 篇
METTL1-mediated m7G modification of Arg-TCT tRNA drives oncogenic transformation
EA Orellana, Q Liu, E Yankova, M Pirouz, E De Braekeleer, W Zhang, ...
Molecular Cell, 2021
强制性开放获取政策： US National Institutes of Health, Cancer Research UK, UK Medical Research …
Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafish
RLP Santos-Cortez, K Lee, AP Giese, M Ansar, M Amin-Ud-Din, K Rehn, ...
Human molecular genetics 23 (12), 3289-3298, 2014
强制性开放获取政策： US National Institutes of Health
ADAMTS1, MPDZ, MVD, and SEZ6: candidate genes for autosomal recessive nonsyndromic hearing impairment
T Bharadwaj, I Schrauwen, S Rehman, K Liaqat, A Acharya, APJ Giese, ...
European Journal of Human Genetics 30 (1), 22-33, 2022
强制性开放获取政策： US National Institutes of Health
Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment
K Liaqat, S Hussain, M Bilal, A Nasir, A Acharya, RH Ali, S Nawaz, ...
Journal of human genetics 65 (2), 187-192, 2020
强制性开放获取政策： US National Institutes of Health
Sequence variants in nine different genes underlying rare skin disorders in 10 consanguineous families
K Shah, S Mehmood, A Jan, I Abbe, R Hussain Ali, A Khan, MS Chishti, ...
International journal of dermatology 56 (12), 1406-1413, 2017
强制性开放获取政策： US National Institutes of Health
Mitral regurgitation as a phenotypic manifestation of nonphotosensitive trichothiodystrophy due to a splice variant in MPLKIP
K Shah, RH Ali, M Ansar, K Lee, MS Chishti, I Abbe, B Li, JD Smith, ...
BMC medical genetics 17 (1), 13, 2016
强制性开放获取政策： US National Institutes of Health
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