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genetic homozygosity (9) 9
medicine, general & internal (7) 7
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Genetika, ISSN 0534-0012, 2015, Volume 47, Issue 2, pp. 765 - 776
This population-genetic study compares morphophysiological and genetic variability in a group of homosexually oriented individuals from Serbia (N=96) with... 
Genetic homozygosity | Homorecessive characteristics | Anthropogenetic variability | Homosexuals | anthropogenetic variability | genetic homozygosity | AGRONOMY | ABO BLOOD-GROUPS | GENETICS & HEREDITY | homorecessive characteristics | MORPHOGENETIC VARIABILITY | homosexuals
Journal Article
Genetika, ISSN 0534-0012, 2016, Volume 48, Issue 2, pp. 743 - 751
This population-genetic study compares morpholophysiological and genetic variability in five control groups of individuals (children from five regular schools,... 
School children | Genetic homozygosity | Anthropogenetic variability | genetic homozygosity | anthropogenetic variability | AGRONOMY | GENETICS & HEREDITY | school children
Journal Article
Genetika, ISSN 0534-0012, 2017, Volume 49, Issue 3, pp. 1035 - 1045
Assuming that developmental hip dysplasia (DDH) is a genetically controlled disease, we made a hypothesis that an increased homozygosity level and genetic... 
Developmental hip dysplasia | Morphogenetic variability | Genetic loads | Homozygously recessive characteristics | morphogenetic variability | AGRONOMY | homozygously recessive characteristics | developmental hip dysplasia | genetic loads | GENETICS & HEREDITY
Journal Article
Journal of Sports Sciences, ISSN 0264-0414, 07/2009, Volume 27, Issue 9, pp. 941 - 947
Journal Article
JOURNAL OF CLINICAL MEDICINE, ISSN 2077-0383, 07/2018, Volume 7, Issue 7, p. 162
In this study, we evaluated and compared the morphogenetic variability and the degree of recessive homozygosity in patients with manifested ischemic stroke... 
MEDICINE, GENERAL & INTERNAL | SUSCEPTIBILITY | homozygous recessive characteristics | POPULATION GENETIC ANALYSES | manifested ischemic stroke | variability | hypertension
Journal Article
BRAIN SCIENCES, ISSN 2076-3425, 06/2019, Volume 9, Issue 6, p. 138
The aim of our study was to evaluate the role of morphogenetic variability in functional outcome of patients with ischemic stroke. The prospective study... 
RECOVERY | functional outcome | SUSCEPTIBILITY | DISABILITY | homozygous recessive characteristics | POPULATION GENETIC ANALYSES | REHABILITATION | stroke | NEUROSCIENCES | age | PLASTICITY
Journal Article
JOURNAL OF CLINICAL MEDICINE, ISSN 2077-0383, 09/2018, Volume 7, Issue 9, p. 232
Background: The aim of our study was to evaluate the degree of genetic homozygosity in the group of patients with coronary artery disease (CAD), as well as to... 
coronary artery disease | blood groups | POPULATION | risk factors | EVENTS | ABO BLOOD-GROUPS | SUSCEPTIBILITY | PREVENTION | RISK | SPINA-BIFIDA OCCULTA | homozygously-recessive characteristics | variability | MEDICINE, GENERAL & INTERNAL | MORPHOGENETIC VARIABILITY | PRAVASTATIN | CORONARY-HEART-DISEASE
Journal Article
JOURNAL OF CLINICAL MEDICINE, ISSN 2077-0383, 05/2018, Volume 7, Issue 5, p. 103
We analyzed morphogenetic variability and degree of genetic homozygosity in male and female individuals with coronary artery disease (CAD) versus unaffected... 
coronary artery disease | MEDICINE, GENERAL & INTERNAL | gender | SUSCEPTIBILITY | homozygous recessive characteristics | UPDATE | variability | HYPERTENSION | TYPE-2 DIABETES-MELLITUS
Journal Article
Archives of Biological Sciences, ISSN 0354-4664, 2014, Volume 66, Issue 3, pp. 1055 - 1059
Myelodysplastic syndromes (MDS) are clonal hematologic stem cell disorders with an as yet unknown molecular pathology. Genetic instability has been proposed as... 
657DEL5 | MDS | NBS1 mutations | Nibrin | CELLS | COMPLEX | PROTEIN | NIJMEGEN BREAKAGE SYNDROME | DNA-DAMAGE RESPONSE | REPAIR | TELOMERE DYSFUNCTION | 657del5 | BIOLOGY | nibrin | ATAXIA-TELANGIECTASIA | APLASTIC-ANEMIA | ASSOCIATION
Journal Article
Archives of Medical Science, ISSN 1734-1922, 12/2011, Volume 7, Issue 6, pp. 1049 - 1054
Introduction: Patients with spina bifida in the lumbosacral region usually have various degrees of motor and sensory dysfunctions of the lower extremities and... 
Muscles | Electromyography | Neurogenic lesion | Spina bifida aperta | Spina bifida occulta | MEDICINE, GENERAL & INTERNAL | muscles | MANAGEMENT | spina bifida occulta | electromyography | NEURAL-TUBE DEFECTS | spina bifida aperta | neurogenic lesion | OCCULTA | DYSRAPHISM | CHILDREN | Clinical Research
Journal Article
Archives of Biological Sciences, ISSN 0354-4664, 2014, Volume 66, Issue 2, pp. 729 - 734
The effect of 5,10-methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphism on serum lipid profiles is controversial. We randomly selected 530... 
Schoolchildren | MTHFR gene | MTHFR 677T allele | Lipid levels | Atherosclerosis | Polymorphism | atherosclerosis | schoolchildren | lipid levels | polymorphism
Journal Article
Archives of Medical Science, ISSN 1734-1922, 12/2010, Volume 6, Issue 6, pp. 854 - 859
Introduction: Assuming that spina bifida (SB) is a genetically controlled disease, the aim of our study was to evaluate the degree of genetic homozygosity and... 
Spina bifida | Genetic homozygosity | Genetic variability | genetic homozygosity | MEDICINE, GENERAL & INTERNAL | spina bifida | NEURAL-TUBE DEFECTS | genetic variability | Basic Research
Journal Article
Archives of Medical Science, ISSN 1734-1922, 11/2012, Volume 8, Issue 6, p. 998
  Introduction: Obesity is a complex condition with multifactorial origin. Assuming that such a state is genetically controlled, the aim of our study was to... 
Journal Article
Addiction Research & Theory, ISSN 1606-6359, 2008, Volume 16, Issue 4, pp. 331 - 337
Acting on the assumption that susceptibility to alcohol dependence is genetically controlled, we have developed a hypothesis that a generally increased... 
HRC test | genetic variation | preventive medicine | Genetic variation | Preventive medicine | SOCIAL ISSUES | SUBSTANCE ABUSE | CHROMOSOME-1
Journal Article
Archives of Biological Sciences, ISSN 0354-4664, 2012, Volume 64, Issue 2, pp. 787 - 792
Duchenne and Becker muscular dystrophy (DMD/BMD) are severe X-linked neuromuscular disorders caused by mutations in the dystrophin gene. Our aim was to... 
SYBR | green | Real-time PCR | Duchenne/Becker muscular dystrophy | carrier detection | ΔΔCt method | DIAGNOSIS | DUPLICATIONS | SYBR (R) Green | DMD/BMD | DMD GENE | IDENTIFICATION | FEMALE CARRIERS | Delta Delta Ct method | POLYMERASE-CHAIN-REACTION | BIOLOGY | DUCHENNE MUSCULAR-DYSTROPHY | DELETIONS | SYBR® Green
Journal Article
Archives of Medical Science, ISSN 1734-1922, 12/2012, Volume 8, Issue 6, pp. 998 - 1002
Introduction: Obesity is a complex condition with multifactorial origin. Assuming that such a state is genetically controlled, the aim of our study was to... 
Obesity | Genetic homozygosity | Genetic variability | Overweight | genetic homozygosity | MEDICINE, GENERAL & INTERNAL | MASS | PHYSICAL-ACTIVITY | INDEX | overweight | obesity | genetic variability | Clinical Research
Journal Article
Genes & Genomics(구 한국유전학회지), ISSN 1976-9571, 2005, Volume 27, Issue 1, p. 35
Our study of genetic homozygosity degree includes an analysis of the presence, distribution and individual combination of 20 to 30 selected genetically... 
genetic homozygosity | ABO blood types | genetic variation
Journal Article
Srpski Arhiv za Celokupno Lekarstvo, ISSN 0370-8179, 2008, Volume 136, Issue 9-10, pp. 519 - 523
INTRODUCTION Our study of genetic homozygosity degree includes an analysis of the presence, distribution and individual combination of 15 selected genetically... 
Hrc-test | Genetic homozygosity | Spinal dysraphia | genetic homozygosity | spinal dysraphia | HRC-test
Journal Article
SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, ISSN 0370-8179, 09/2008, Volume 136, Issue 9-10, pp. 519 - 523
INTRODUCTION Our study of genetic homozygosity degree includes an analysis of the presence, distribution and individual combination of 15 selected genetically... 
genetic homozygosity | MEDICINE, GENERAL & INTERNAL | BIFIDA | spinal dysraphia | NEURAL-TUBE DEFECTS | INHERITANCE | LOCUS | HRC-test | FAMILY | Homozygote | Phenotype | Child | Humans | Spinal Dysraphism - genetics | Index Medicus
Journal Article
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