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Palavra-chave:
genetics
utilizada 151 vezes por 25 professores
Utilizada por 25 professores
Por ordem de relevância (total: 25)
Patrícia Maria de Carvalho Aguiar
Maria Cristina de Oliveira Izar
Laercio Joel Franco
Henrique Ballalai Ferraz
Vanderci Borges
André Fernandes Reis
Francisco Antonio Helfenstein Fonseca
José Antônio Baddini Martinez
Juliana Maria Ferraz Sallum
Adriana Berezovsky
Delcio Matos
Isabel Cristina Céspedes
Laura Maria de Figueiredo Ferreira Guilhoto
Marcelo Marcos Piva Demarzo
Marcelo Visentini Kitahara
Solange Rios Salomão
Adauto Castelo Filho
Alexandre Wagner Silva de Souza
Antônio Carlos de Camargo Carvalho
Elvira Maria Guerra Shinohara
Elza Márcia Targas Yacubian
Lia Rita Azeredo Bittencourt
Rodrigo Affonseca Bressan
Solange Andreoni
Vera Lucia Sdepanian
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ATP1A3
Acculturation
Aculturation
Alcohol
Apolipoproteins
Atenção primária à saúde
Brazilian Indians
COMT gene
CYP2A6
Cataracts
Celiac disease
Cobalamin
Cognition
Colorectal Adenocarcinoma
DIABETES
DYT1
DYT25
DYT6
Diabetes Mellitus
Diagnosis
Distonia
Dyslipidemia
Dystonia
EEG
Endothelium
Epidemiologia
Epilepsy
Essential myoclonus
Ethnicity and health
Eye diseases
Familial hypercholesterolemia
Familial interstitial pneumonias
Folate
Friedreich ataxia
Functional Genomics
GNAL
Gene Expression
Genetica Medica
Gilles de la Tourette
HEREDITARY
HLA
HLA DQB1*0602 allele
Homocysteine
Huntington's disease
Japanese-Brazilians
LHON
LRRK2
Lafora Body Disease
MODY
MTHFR
MYOCARDIAL INFARCTION
Marfan Syndrome
Medical education
Microarray
Molecular biology
Multiple System Atrophy
Mutation
Myoclonus
NGS
NPC1
New Caledonia
Niemann Pick
Non- motor symptoms
PARK2
PARK8
PINK1
PRKRA
PROM 1 protein
Parkin
Parkinson
Parkinson's disease
Polymorphism
Polymorphisms
Positron-emission tomography
Primary Health Care
Retinal dystrophies
Review
SGCE
Scleractinia
Single photon emission computed tomography
Smoking
Survival
THAP1
TRODAT
Treatment outcome
Triglycerides
Type 2 diabetes
UCP2
WFS1 gene
adiponectina
association study
atypical parkinsonism
autophagy
azooxanthellate
birth weight
cholesterol
chronic complications
cocaine dependence
color vision
congenital
coronary heart disease
diabetes type 2
distonia-mioclonia
educação médica
environment
epidemiology
fatores de risco
febrile seizure
genetics
genomic imprinting
glucoquinase
glucose intolerance
glucose tolerance
gold
human
imaging
insulin secretion
insulin-dependent diabetes mellitus
integrin genes
likage
lipids
lipoprotein lipase
macrovascular disease
matematic model
migraine
mitonchondria
molecular imaging
myoclonus-dystonia
narcolepsy
neuro-ophthalmology
neurodegeneration
neuroimage
obesidade
obsessive-compulsive disorder
ocular abnomalities
optic nerve
osteoporosis
pakinson's disease
parkinsonism
phylogeny
rapid-onset dystonia parkinsonism
segregation analysis
síndrome metabólica
taxonomy
visual impairment: neuro-ophthalmological disease
vitamin D receptor gene polymorfism
wolframin
índios brasileiros
CTIT UFMG