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1.
Autozygosity-driven genetic diagnosis in consanguineous families from Italy and the Greater Middle East.
Hum Genet
; 139(11): 1429-1441, 2020 Nov.
Article
in English
| MEDLINE | ID: mdl-32488467
2.
In silico analysis of a novel causative mutation in Cadherin23 gene identified in an Omani family with hearing loss.
J Genet Eng Biotechnol
; 18(1): 8, 2020 Mar 02.
Article
in English
| MEDLINE | ID: mdl-32115674
3.
Novel mutation of GLRA1 in Omani families with hyperekplexia and mild mental retardation.
Pediatr Neurol
; 46(2): 89-93, 2012 Feb.
Article
in English
| MEDLINE | ID: mdl-22264702
4.
Apolipoprotein E polymorphism in Omani dyslipidemic patients with and without coronary artery disease.
Hum Biol
; 79(1): 93-102, 2007 Feb.
Article
in English
| MEDLINE | ID: mdl-17985658
5.
Distribution of apolipoprotein E alleles in the Omani population.
Med Princ Pract
; 14(2): 73-8, 2005.
Article
in English
| MEDLINE | ID: mdl-15785096
6.
Apolipoprotein A1 gene polymorphisms at the -75 bp and +83/ 84 bp polymorphic sites in healthy Omanis compared with world populations.
Hum Biol
; 76(2): 307-12, 2004 Apr.
Article
in English
| MEDLINE | ID: mdl-15359539
7.
Clinical and molecular analysis of Grebe acromesomelic dysplasia in an Omani family.
Am J Med Genet A
; 121A(1): 9-14, 2003 Aug 15.
Article
in English
| MEDLINE | ID: mdl-12900894
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