Detalhe da pesquisa
1.
Exome sequencing unravels genetic variants associated with chronic kidney disease in Saudi Arabian patients.
Hum Mutat
; 43(12): e24-e37, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36177613
2.
A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian families.
J Hum Genet
; 58(7): 480-9, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23595123
3.
Genetic diagnosis in consanguineous families with kidney disease by homozygosity mapping coupled with whole-exome sequencing.
Am J Kidney Dis
; 58(2): 186-95, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21658830
4.
Renal failure associated with APECED and terminal 4q deletion: evidence of autoimmune nephropathy.
Clin Dev Immunol
; 2010: 586342, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-21197407
5.
Novel mutations underlying nephrogenic diabetes insipidus in Arab families.
Genet Med
; 8(7): 443-7, 2006 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-16845277