Suchergebnisse - "Waryah, Yar Muhammad"

PubPharm (13)

1

Serum and salivary Cu/Zn ratio as a diagnostic biomarker for oral submucosal fibrosis : an analysis of trace metals and LOX gene variants

enthalten in: Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine | 2024

von Shah, R. | Khidri, F. | Waryah, Y. | +6

2

Serum and salivary Cu/Zn ratio as a diagnostic biomarker for oral submucosal fibrosis: an analysis of trace metals and LOX gene variants

enthalten in: BioMetals | 2023

von Shah, R. | Khidri, F. | Waryah, Y. | +6

3

Impact of ACE2 gene variations on COVID-19 pathogenicity in Pakistani patients

enthalten in: Saudi journal of biological sciences | 2023

von Waryah, Y. | Khidri, F. | Nigar, R. | +4

4

Association of MSX1 Gene Variants with Nonsyndromic Cleft Lip and/or Palate in the Pakistani Population

enthalten in: The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association | 2023

von Memon, A. | Khidri, F. | Waryah, Y. | +5

5

Delineating the Spectrum of Genetic Variants Associated with Bardet-Biedl Syndrome in Consanguineous Pakistani Pedigrees

enthalten in: Genes | 2023

von Rao, A. | Nazir, A. | Imtiaz, S. | +12

6

Association of single nucleotide polymorphism variations in CRYAA and CRYAB genes with congenital cataract in Pakistani population

enthalten in: Saudi journal of biological sciences | 2022

von Jarwar, P. | Waryah, Y. | Rafiq, M. | +1

7

Biallelic Variants in EPHA2 Identified in Three Large Inbred Families with Early-Onset Cataract

enthalten in: International journal of molecular sciences | 2021

von Jarwar, P. | Sheikh, S. | Waryah, Y. | +4

8

P.arg102ser is a common Pde6a mutation causing autosomal recessive retinitis pigmentosa in Pakistani families

enthalten in: JPMA. The Journal of the Pakistan Medical Association | 2021

von Khan, A. | Waryah, Y. | Iqbal, M. | +3

9

MTHFR and F5 genetic variations have association with preeclampsia in Pakistani patients : a case control study

enthalten in: BMC medical genetics | 2019

von Khidri, F. | Waryah, Y. | Ali, F. | +3

10

MTHFR and F5 genetic variations have association with preeclampsia in Pakistani patients: a case control study

enthalten in: BMC medical genetics | 2019

von Khidri, F. | Waryah, Y. | Ali, F. | +3