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Jelani, Musharraf
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1

Unveiling genetics of non-syndromic albinism using whole ex..:

Zaman, Qaiser ; Khan, Jamshid ; Ahmad, Mashal...
Gene.  894 (2024)  - p. 147986 , 2024
Link: https://doi.org/10.1016/..
 
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2

Phenotypic Classification of Eye Colour and Developmental V..:

Rahat, Murad Ali ; Akbar, Fazal ; Rasool, Akhtar...
Biomedicines.  11 (2023)  4 - p. 1228 , 2023
Link: https://doi.org/10.3390/..
 
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3

Two novel homozygous variants of ATP6V0A2 and ALDH18A1 lead..:

Zaman, Qaiser ; Iftikhar, Aiman ; Rehman, Gauhar...
The Journal of Gene Medicine.  25 (2023)  10 - p. , 2023
Link: https://doi.org/10.1002/..
 
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4

A Novel Homozygous Nonsense Variant in the DYM Underlies Dy..:

Bakar, Abu ; Shams, Sulaiman ; Bibi, Nousheen...
Genes.  14 (2023)  2 - p. 510 , 2023
Link: https://doi.org/10.3390/..
 
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5

Report of Hermansky–Pudlak Syndrome in Two Families with No..:

Zaman, Qaiser ; Sadeeda ; Anas, Muhammad...
Genes.  14 (2023)  1 - p. 145 , 2023
Link: https://doi.org/10.3390/..
 
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6

Novel Variants in MPV17, PRX, GJB1, and SACS Cause Charcot–..:

Zaman, Qaiser ; Khan, Muhammad Abbas ; Sahar, Kalsoom...
Genes.  14 (2023)  2 - p. 328 , 2023
Link: https://doi.org/10.3390/..
 
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7

Whole exome sequencing identified five novel variants in CN..:

Abdulkareem, Angham Abdulrhman ; Zaman, Qaiser ; Khan, Hamza...
Frontiers in Genetics.  14 (2023)  - p. , 2023
Link: https://doi.org/10.3389/..
 
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8

Association of cytochromes P450 3A4*22 and 3A5*3 genotypes ..:

Elalem, Elbatool G. ; Jelani, Musharraf ; Khedr, Alaa...
PLOS ONE.  17 (2022)  7 - p. e0260824 , 2022
Link: https://doi.org/10.1371/..
 
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9

Whole exome sequencing identifies a novel compound heterozy..:

Khan, Atta Ullah ; Khan, Ibrar ; Khan, Muhammad Ismail...
American Journal of Medical Genetics Part A.  188 (2022)  9 - p. 2693-2700 , 2022
Link: https://doi.org/10.1002/..
 
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10

Two missense mutations in GPNMB cause autosomal recessive a..:

Rahman, Obaid Ur ; Kim, Jeena ; Mahon, Caroline..
Genes & Genomics.  43 (2021)  5 - p. 471-478 , 2021
Link: https://doi.org/10.1007/..
 
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11

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/..
 
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12

Whole exome sequencing reveals a homozygous SGCB variant in..:

Tariq, Muhammad ; Latif, Muhammad ; Inam, Memona...
Gene Reports.  22 (2021)  - p. 101014 , 2021
Link: https://doi.org/10.1016/..
 
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13

Biallelic inheritance in a single Pakistani family with int..:

Pastore, Stephen F. ; Muhammad, Tahir ; Harripaul, Ricardo...
Scientific Reports.  11 (2021)  1 - p. , 2021
Link: https://doi.org/10.1038/..
 
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14

A novel variant in theDSEgene leads toEhlers–Danlosmusculoc..:

Ullah, Ikram ; Aamir, Muhammad ; Ilyas, Muhammad...
Congenital Anomalies.  61 (2021)  5 - p. 177-182 , 2021
Link: https://doi.org/10.1111/..
 
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15

Genetic variations in drug-metabolizing enzyme CYP2C9 among..:

Hizbullah ; Ahmed, Sagheer ; Noor Mumtaz, Mah...
Gene.  746 (2020)  - p. 144659 , 2020
Link: https://doi.org/10.1016/..
 
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