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1.
Novel variants underlying autosomal recessive intellectual disability in Pakistani consanguineous families.
BMC Med Genet
; 21(1): 59, 2020 03 24.
Article
in English
| MEDLINE | ID: mdl-32209057
2.
Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family.
Hum Genet
; 133(8): 975-84, 2014 Aug.
Article
in English
| MEDLINE | ID: mdl-24623383
3.
A novel single base pair duplication in WDR62 causes primary microcephaly.
BMC Med Genet
; 15: 107, 2014 Oct 11.
Article
in English
| MEDLINE | ID: mdl-25303973
4.
Exploring evolution of brain genes involved in microcephaly through phylogeny and synteny analysis.
Theor Biol Med Model
; 10: 61, 2013 Oct 22.
Article
in English
| MEDLINE | ID: mdl-24148351
5.
Unveiling forensically relevant biogeographic, phenotype and Y-chromosome SNP variation in Pakistani ethnic groups using a customized hybridisation enrichment forensic intelligence panel.
PLoS One
; 17(2): e0264125, 2022.
Article
in English
| MEDLINE | ID: mdl-35176104
6.
In silico studies of C 3 metabolic pathway proteins of wheat (Triticum aestivum).
Biomed Res Int
; 2013: 294759, 2013.
Article
in English
| MEDLINE | ID: mdl-23484105
7.
Identification of novel mutation in the HR gene responsible for atrichia with papular lesions in a Pakistani family.
J Dermatol
; 40(11): 927-8, 2013 Nov.
Article
in English
| MEDLINE | ID: mdl-24111842
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