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Khan, Hammal
32  results:
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1

Novel pathogenic variants in HR underlie atrichia with papu..:

Ullah, Kifayat ; Ahmed, Sohail ; Cesarato, Nicole...
The Journal of Dermatology.  , 2024
Link: https://doi.org/10.1111/..
 
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2

Loss-of-function variant in the LRR domain of SLITRK2 impli..:

Afsar, Tayyaba ; Fu, Hongxia ; Khan, Hammal...
Frontiers in Genetics.  14 (2024)  - p. , 2024
Link: https://doi.org/10.3389/..
 
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3

A novel homozygous FAM92A gene (CIBAR1) variant further con..:

Umair, Muhammad ; Ahmed, Zaheer ; Shaker, Bilal...
Clinical Genetics.  , 2024
Link: https://doi.org/10.1111/..
 
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4

Clinical and genetic investigation of 14 families with vari..:

Khan, Fati Ullah ; Khan, Hammal ; Ullah, Kifayat...
Clinical Genetics.  , 2024
Link: https://doi.org/10.1111/..
 
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5

Sequence variants in DLX5, HOXD13 and 445 kb‐microduplicati..:

Abdullah ; Hussain, Shabir ; Ji, Weizhen...
Clinical Genetics.  105 (2023)  1 - p. 109-111 , 2023
Link: https://doi.org/10.1111/..
 
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6

A variant in the LDL receptor‐related protein encoding gene..:

Khan, Hammal ; Ullah, Kifayat ; Jan, Abid...
Congenital Anomalies.  63 (2023)  6 - p. 190-194 , 2023
Link: https://doi.org/10.1111/..
 
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7

Variants in EFCAB7 underlie nonsyndromic postaxial polydact..:

Bilal, Muhammad ; Khan, Hammal ; Khan, Muhammad Javed...
European Journal of Human Genetics.  31 (2023)  11 - p. 1270-1274 , 2023
Link: https://doi.org/10.1038/..
 
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8

A splice site variant in TCTN3 underlies an atypical form o..:

Hussain, Shabir ; Nawaz, Shoaib ; Khan, Hammal...
Annals of Human Genetics.  86 (2022)  6 - p. 291-296 , 2022
Link: https://doi.org/10.1111/..
 
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9

A novel variant in AFF3 underlying isolated syndactyly:

Khan, Hammal ; Koh, Glenn ; Chong, Angie En Qi...
Clinical Genetics.  103 (2022)  3 - p. 341-345 , 2022
Link: https://doi.org/10.1111/..
 
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10

A novel homozygous variant in the GLI1 underlies postaxial ..:

Bakar, Abu ; Ullah, Asmat ; Bibi, Nousheen...
European Journal of Medical Genetics.  65 (2022)  10 - p. 104599 , 2022
Link: https://doi.org/10.1016/..
 
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11

Novel variants in the LRP4 underlying Cenani-Lenz Syndactyl..:

Khan, Hammal ; Chong, Angie En Qi ; Bilal, Muhammad...
Journal of Human Genetics.  67 (2021)  5 - p. 253-259 , 2021
Link: https://doi.org/10.1038/..
 
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12

A splice site variant in TCTN3 underlies an atypical form o..:

Hussain, Shabir ; Nawaz, Shoaib ; Khan, Hammal...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804382/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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13

Loss-of-function variant in the LRR domain of SLITRK2 impli..:

Tayyaba Afsar ; Hongxia Fu ; Hammal Khan...
https://www.frontiersin.org/articles/10.3389/fgene.2023.1308116/full.  , 2024
Link: https://doi.org/10.3389/..
 
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14

Uncovering the genetic basis of hyperphosphatasia with impa..:

Anam Nayab ; Shagufta Andleeb ; Shah Zeb...
http://www.ejmanager.com/fulltextpdf.php?mno=137867.  , 2023
Link: https://doi.org/10.24911..
 
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15

Genetic advances in skeletal disorders: an overview:

Safdar Abbas ; Hammal Khan ; Qamre Alam..
http://www.ejmanager.com/fulltextpdf.php?mno=134070.  , 2023
Link: https://doi.org/10.24911..
 
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