Detalhe da pesquisa
1.
Biallelic missense variants in ZBTB11 can cause intellectual disability in humans.
Hum Mol Genet
; 27(18): 3177-3188, 2018 09 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29893856
2.
Heterozygosity for the Novel HBA2: c.*91_*92delTA Polyadenylation Site Variant on the α2-Globin Gene Expanding the Genetic Spectrum of α-Thalassemia in Iran.
Hemoglobin
; 44(6): 423-426, 2020 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-33054440
3.
Effect of inbreeding on intellectual disability revisited by trio sequencing.
Clin Genet
; 95(1): 151-159, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30315573
4.
Frequency of α-Globin Gene Triplications and Coinheritance with ß-Globin Gene Mutations in the Iranian Population.
Hemoglobin
; 42(4): 252-256, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-30451045
5.
Identification of causative gene mutation in an Iranian family with coloboma and nephropathy using whole exome sequencing.
CEN Case Rep
; 11(4): 404-407, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35179696