E-LIB Suche - Ergebnisse für: Jan, Abid

1

Unraveling the Challenges of Oxidative Stability and Method..:

Zulfiqar, Hira ; Ahmed, Iqbal ; Farooq, Muhammad Furqan...
Journal of Chemistry and Environment. , 2023

Link: https://doi.org/10.56946..

2

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/..

3

The Effectiveness of High Intensity Electromagnetic Stimula..:

Khan, Muslim ; Ali, Aftab ; Khan, Zakir...
Pakistan BioMedical Journal. , 2023

Link: https://doi.org/10.54393..

4

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/..

5

Biallelic mutations in FLG, TGM1, and STS genes segregated ..:

Khan, Niamatullah ; Shah, Khadim ; Fozia, Fozia...
International Journal of Dermatology. 62 (2023) 5 - p. 672-680 , 2023

Link: https://doi.org/10.1111/..

6

Clinical Profile of the Stroke Recovering Patients in the A..:

Khan, Muslim ; Ali, Aftab ; Khan, Zakir...
Pakistan BioMedical Journal. , 2023

Link: https://doi.org/10.54393..

7

Vortex-assisted liquid-liquid microextraction of selected n..:

Jan, Abid ; Shah, Jasmin ; Jan, Muhammad Rasul
Desalination and Water Treatment. 261 (2022) - p. 289-298 , 2022

Link: https://doi.org/10.5004/..

8

Mutation screening of multiple Pakistani MCPH families reve..:

Hussain, Sadam ; Nawaz, Amjad ; Hamid, Malaika...
Biotechnology and Applied Biochemistry. 69 (2021) 6 - p. 2296-2303 , 2021

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

9

A novel homozygous sequence variant in GLI1 underlies first..:

Ullah, Asmat ; Umair, Muhammad ; Majeed, Ayesha I....
Clinical Genetics. 95 (2019) 4 - p. 540-541 , 2019

Link: https://doi.org/10.1111/..

10

Sequence variants in GDF5 and TRPS1 underlie brachydactyly ..:

Ullah, Asmat ; Umair, Muhammad ; Hussain, Shabir..
Pediatrics International. 60 (2018) 3 - p. 304-306 , 2018

Link: https://doi.org/10.1111/..

11

A variant in LMX1A causes autosomal recessive severe-to-pro..:

Schrauwen, Isabelle ; Chakchouk, Imen ; Liaqat, Khurram...
Human Genetics. 137 (2018) 6-7 - p. 471-478 , 2018

Link: https://doi.org/10.1007/..

12

Ellis–van Creveld syndrome and profound deafness resulted b..:

Umair, Muhammad ; Seidel, Heide ; Ahmed, Ishtiaq...
Journal of Genetics. 96 (2017) 6 - p. 1005-1014 , 2017

Link: https://doi.org/10.1007/..

13

Exome sequencing reveals a novel homozygous splice site var..:

Umair, Muhammad ; Alhaddad, Bader ; Rafique, Afzal...
Pediatric Research. 82 (2017) 5 - p. 753-758 , 2017

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

14

Sequence variants in nine different genes underlying rare s..:

Shah, Khadim ; Mehmood, Sabba ; Jan, Abid...
International Journal of Dermatology. 56 (2017) 12 - p. 1406-1413 , 2017

Link: https://doi.org/10.1111/..

15

Spectrofluorimetric Method for Quantification of Triazine H..:

Muhammad, Mian ; Shah, Jasmin ; Jan, M. Rasul...
Analytical Sciences. 32 (2016) 3 - p. 313-316 , 2016

Link: https://doi.org/10.2116/..