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BMC Evolutionary Biology, ISSN 1471-2148, 06/2018, Volume 18, Issue 1, pp. 98 - 98
Journal Article
BMC evolutionary biology, 11/2016, Volume 16, Issue 1, pp. 246 - 246
From a mtDNA dominant perspective, the exit from Africa of modern humans to colonize Eurasia occurred once, around 60 kya, following a southern coastal route... 
Genetics, Population | Humans | Phylogeography | Africa | Genetic Markers | Phylogeny | Fossils | India | Asia, Southeastern | Genetic Variation | Archaeology | Haplotypes - genetics | DNA, Mitochondrial - genetics | Asia | Heterozygote | Australia | Far East | Human Migration | Principal Component Analysis | Cluster Analysis | Index Medicus
Journal Article
Journal of AAPOS, ISSN 1091-8531, 12/2014, Volume 18, Issue 6, pp. 622 - 623
Journal Article
Journal of AAPOS, ISSN 1091-8531, 12/2014, Volume 18, Issue 6, pp. 622 - 623
Journal Article
BMC Research Notes, ISSN 1756-0500, 11/2017, Volume 10, Issue 1, pp. 562 - 562
Congenital fibrosis of the extraocular muscles type 1 (CFEOM1) is known to be caused by mutations in KIF21A or TUBB3 or other known genes (SALL4, CHN1, HOXA1).... 
Congenital fibrosis | arrayCGH | GRHL2 | CCDD | Psychological aspects | Genetic disorders | Fibrosis | Muscles | Research | Gene expression | Face | Index Medicus
Journal Article
Journal of American Association for Pediatric Ophthalmology and Strabismus, ISSN 1091-8531, 12/2014, Volume 18, Issue 6, pp. 622 - 623
Journal Article
Prenatal Diagnosis, ISSN 0197-3851, 02/2014, Volume 34, Issue 2, pp. 153 - 158
What's already known about this topic? In the Saudi society, attitude toward prenatal diagnosis and termination of pregnancy is influenced by the severity of... 
ADULTS | PREVALENCE | THALASSEMIA | GENETICS & HEREDITY | OBSTETRICS & GYNECOLOGY | Deafness | Prenatal Diagnosis - psychology | Attitude to Health | Humans | Male | Pregnancy | Saudi Arabia | Abortion, Eugenic - psychology | Parents - psychology | Sex Factors | Adult | Female | Surveys and Questionnaires | Culture | Pregnant women | Alzheimer's disease | Analysis | Deaf | Amyloid beta-protein | Index Medicus
Journal Article
BMC Research Notes, ISSN 1756-0500, 11/2017, Volume 10, Issue 1, pp. 652 - 652
Polymorphism rs13334190 in the zinc finger protein 469 gene has been suggested to predispose toward a "thin" cornea, which then becomes keratoconic or is... 
rs13334190 | ZNF469 | Saudi | Keratoconus | Medical colleges | Genetic aspects | DNA binding proteins | Genes | Risk factors | Index Medicus
Journal Article
Molecular Vision, ISSN 1090-0535, 2011, Volume 17, Issue 74-76, pp. 667 - 672
Purpose: To screen the visual system homebox 1 (VSX1) gene in Saudi Arabian keratoconus patients. Methods: We sequenced the entire coding region, exon-intron... 
LOCALIZATION | DYSTROPHY | FAMILIES | BIOCHEMISTRY & MOLECULAR BIOLOGY | OPHTHALMOLOGY | MUTATIONS | LINKAGE | LOCUS | Genetic Testing | Humans | Middle Aged | Male | Case-Control Studies | Homeodomain Proteins - genetics | Saudi Arabia | Phenotype | Base Sequence | Keratoconus - genetics | Female | Keratoconus - pathology | Eye Proteins - genetics | Index Medicus
Journal Article
Ophthalmic Genetics, ISSN 1381-6810, 01/2019, Volume 40, Issue 1, pp. 74 - 76
Journal Article
Clinical Ophthalmology, ISSN 1177-5467, 01/2018, Volume 12, p. 1413
Cytochrome P450 Family 1 Subfamily B Member 1 (CYP1B1; OMIM# 601771) gene encodes one of the cytochrome P450 family of enzymes. CYP1B1 mutations have been... 
Medicine | Cytochrome | Studies | Glaucoma | Enzymes | Congenital diseases | Pathogenesis | Genes | Cell cycle | Cardiovascular disease | Mutation
Journal Article
Ophthalmic Genetics, ISSN 1381-6810, 12/2015, Volume 36, Issue 4, pp. 373 - 375
We investigated Saudi patients with familial and sporadic Keratoconus for mutations in the Superoxide dismutase 1, soluble (SOD1) gene. We sequenced the entire... 
Saudi Arabia | mutation | SOD1 gene | Keratoconus | OPHTHALMOLOGY | GENETICS & HEREDITY | Superoxide Dismutase - genetics | Humans | Middle Aged | Male | Young Adult | Keratoconus - genetics | Polymerase Chain Reaction | Arabs - genetics | Adult | Female | Mutation | Superoxide Dismutase-1 | Saudi Arabia - epidemiology | Index Medicus
Journal Article
Saudi Medical Journal, ISSN 0379-5284, 09/2015, Volume 36, Issue 9, pp. 1110 - 1114
The aim of this report is to analyze the clinical features, and mutations of the methylmalonyl CoA mutase (MUT) gene in 2 patients with methylmalonic aciduria... 
MEDICINE, GENERAL & INTERNAL | ACIDEMIA | ACIDURIA | Methylmalonyl-CoA Mutase - genetics | Saudi Arabia | Homozygote | Animals | Humans | Mice | Mutation | Amino acids | Genetic aspects | Codon | Genes | Index Medicus | Case Report
Journal Article
Journal of AAPOS, ISSN 1091-8531, 2015, Volume 19, Issue 2, pp. 191 - 192
“Mirror movements” are an axonal guidance disorder that consists of involuntary contralateral movements that mimic unilateral intentional ones, typically... 
Ophthalmology | OPHTHALMOLOGY | PEDIATRICS | Cranial Nerves - abnormalities | Oculomotor Nerve Diseases - congenital | Humans | Movement Disorders - congenital | Strabismus - congenital | Male | Consanguinity | Child | Oculomotor Muscles - innervation | Genetic disorders | Paralysis | Index Medicus
Journal Article
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