Zaman, Qumar
18  results:
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1

Homozygous mutations in C14orf39/SIX6OS1 cause non-obstruct..:

Fan, Suixing ; Jiao, Yuying ; Khan, Ranjha...
The American Journal of Human Genetics.  109 (2022)  7 - p. 1343 , 2022
 
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Homozygous mutations in C14orf39/SIX6OS1 cause non-obstruct..:

Fan, Suixing ; Jiao, Yuying ; Khan, Ranjha...
The American Journal of Human Genetics.  108 (2021)  2 - p. 324-336 , 2021
 
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8

Novel Loss-of-Function Mutations in DNAH1 Displayed Differe..:

Khan, Ranjha ; Zaman, Qumar ; Chen, Jing...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8635859/.  , 2021
 
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9

Computationally predicted pathogenic USP9X mutation identif..:

Wei Liu ; Yue-Wen Wang ; Huan Zhang...
http://www.zoores.ac.cn/EN/10.24272/j.issn.2095-8137.2021.409.  , 2022
 
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13

Novel Loss-of-Function Mutations in DNAH1 Displayed Differe..:

Ranjha Khan ; Qumar Zaman ; Jing Chen...
https://www.frontiersin.org/articles/10.3389/fendo.2021.765639/full.  , 2021
 
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15

Image_2_Novel Loss-of-Function Mutations in DNAH1 Displayed..:

Ranjha Khan (11024895) ; Qumar Zaman (11717246) ; Jing Chen (4762)...
https://figshare.com/articles/figure/Image_2_Novel_Loss-of-Function_Mutations_in_DNAH1_Displayed_Different_Phenotypic_Spectrum_in_Humans_and_Mice_tif/17031398.  , 2021
 
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