E-LIB Suche - Ergebnisse für: Sher Alam Khan

1

Variants in HCFC1 and MN1 genes causing intellectual disabi..:

Hussain, Syeda Iqra ; Muhammad, Nazif ; Shah, Shahbaz Ali...
BMC Medical Genomics. 17 (2024) 1 - p. , 2024

Link: https://doi.org/10.1186/..

2

Professional Quality of Life and Psychological Impact on Fr..:

Ullah, Hanif ; Arbab, Safia ; Liu, Chang-Qing...
Journal of Nursing Management. 2024 (2024) - p. 1-9 , 2024

Link: https://doi.org/10.1155/..

3

Brachyolmia, dental anomalies and short stature (DASS): Phe..:

Nawaz, Hamed ; Parveen, Asia ; Khan, Sher Alam...
Heliyon. 10 (2024) 1 - p. e23688 , 2024

Link: https://doi.org/10.1016/..

4

Biallelic Variants in Seven Different Genes Associated with..:

Nawaz, Hamed ; Mujahid ; Khan, Sher Alam...
Genes. 14 (2023) 5 - p. 1113 , 2023

Link: https://doi.org/10.3390/..

5

Autosomal recessive variants c.953A>C and c.97-1G>C in NSUN..:

Muhammad, Nazif ; Hussain, Syeda Iqra ; Rehman, Zia Ur...
Frontiers in Neurology. 14 (2023) - p. , 2023

Link: https://doi.org/10.3389/..

6

Molecular insight into CREBBP and TANGO2 variants causing i..:

Hussain, Syeda Iqra ; Muhammad, Nazif ; Khan, Niamatullah...
The Journal of Gene Medicine. 26 (2023) 1 - p. , 2023

Link: https://doi.org/10.1002/..

7

A novel frameshift variant in UBA2 causing split-hand/foot ..:

Parveen, Asia ; Tariq, Muhammad ; Khan, Sher Alam...
Human Genome Variation. 10 (2023) 1 - p. , 2023

Link: https://doi.org/10.1038/..

8

Structural and functional implications of SLC13A3 and SLC9A..:

Hussain, Syeda Iqra ; Muhammad, Nazif ; Shah, Salah Ud Din...
BMC Neurology. 23 (2023) 1 - p. , 2023

Link: https://doi.org/10.1186/..

9

The Expansion of the Spectrum in Stuttering Disorders to a ..:

Rehman, Adil U ; Hamid, Malaika ; Khan, Sher Alam...
Genes. 13 (2022) 12 - p. 2299 , 2022

Link: https://doi.org/10.3390/..

10

An analysis of the narrowing space of secularism in India a..:

Alam, Sughra ; Bhatti, Muhammad Nawaz ; Khan, Alam Sher
Liberal Arts and Social Sciences International Journal (LASSIJ). 6 (2022) 2 - p. 122-143 , 2022

Link: https://doi.org/10.47264..

11

The First Report of a Missense Variant in RFX2 Causing Non-..:

Khan, Sher Alam ; Khan, Saadullah ; Muhammad, Noor...
Frontiers in Genetics. 12 (2022) - p. , 2022

Link: https://doi.org/10.3389/..

12

Detection of Novel Biallelic Causative Variants in COL7A1 G..:

Fozia, Fozia ; Nazli, Rubina ; Alrashed, May Mohammed...
Diagnostics. 12 (2022) 7 - p. 1525 , 2022

Link: https://doi.org/10.3390/..

13

Whole Exome Sequencing Confirms Molecular Diagnostics of Th..:

Fozia, Fozia ; Nazli, Rubina ; Bibi, Nousheen...
Frontiers in Pediatrics. 9 (2021) - p. , 2021

Link: https://doi.org/10.3389/..

14

Novel Homozygous Mutations in the Genes TGM1, SULT2B1, SPIN..:

Fozia, Fozia ; Nazli, Rubina ; Alam Khan, Sher...
Genes. 12 (2021) 3 - p. 373 , 2021

Link: https://doi.org/10.3390/..

15

Novel splicing‐site mutation in DCAF17 gene causing Woodhou..:

Fozia, Fozia ; Shah, Khadim ; Nazli, Rubina...
Journal of Clinical Laboratory Analysis. 36 (2021) 1 - p. , 2021

Link: https://doi.org/10.1002/..