Search details
1.
Novel variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability in Iranian consanguineous families.
J Clin Lab Anal
; 36(2): e24241, 2022 Feb.
Article
in English
| MEDLINE | ID: mdl-35019165
2.
Defective phosphatidylethanolamine biosynthesis leads to a broad ataxia-spasticity spectrum.
Brain
; 144(3): e30, 2021 04 12.
Article
in English
| MEDLINE | ID: mdl-33454747
3.
An inappropriate decline in ribosome levels drives a diverse set of neurodevelopmental disorders.
bioRxiv
; 2024 Jan 09.
Article
in English
| MEDLINE | ID: mdl-38260472
4.
A Novel Missense Mutation in the ALDH13 Gene Causes Anophthalmia in Two Unrelated Iranian Consanguineous Families.
Int J Mol Cell Med
; 6(2): 131-134, 2017.
Article
in English
| MEDLINE | ID: mdl-28890889
5.
Incomplete penetrance of autosomal recessive anophthalmia in a large consanguineous family.
Ophthalmic Genet
; 42(6): 787-789, 2021 12.
Article
in English
| MEDLINE | ID: mdl-34287093
6.
Prevalence of glucose-6-phosphate dehydrogenase (G6PD) deficiency in southeast Iran: implications for malaria elimination.
J Infect Dev Ctries
; 9(3): 289-97, 2015 Mar 15.
Article
in English
| MEDLINE | ID: mdl-25771467
Results
1 -
6
de 6
1
Next >
>>