Keywords: سندرم حذف 22q11; DNA copy number variations; Congenital heart defects; 22q11 deletion syndrome; Comparative genomic hybridization; Chromosome aberrations; Variações do número de cópias de DNA; Cardiopatias congênitas; SÃndrome de deleção 22q11; Hibridização genÃ
مقالات ISI سندرم حذف 22q11 (ترجمه نشده)
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Keywords: سندرم حذف 22q11; DNA copy number variations; Congenital heart defects; 22q11 deletion syndrome; Comparative genomic hybridization; Chromosome aberrations; Variações do número de cópias de DNA; Cardiopatias congênitas; SÃndrome de deleção 22q11; Hibridização genÃ
Keywords: سندرم حذف 22q11; United Kingdom; Biosociality; Collective effervescence; Conferences; Rare disease community; 22q11 deletion syndrome; Ceremonial order;
Dopamine in high-risk populations: A comparison of subjects with 22q11.2 deletion syndrome and subjects at ultra high-risk for psychosis
Keywords: سندرم حذف 22q11; 22q11 deletion syndrome; Ultra High Risk Psychosis; Dopamine; SPECT;
The use of two different MLPA kits in 22q11.2 deletion syndrome
Keywords: سندرم حذف 22q11; 22q11 deletion syndrome; Cognitive deterioration; Intelligence; Psychopathology; MLPA; Deletion size
La dysgénésie thymique : marqueur de microdélétion 22q11.2 dans le bilan d'un hydramnios
Keywords: سندرم حذف 22q11; Syndrome de Di George; Microdélétion 22q11.2; Hydramnios; Thymus fÅtal; Ãchographie anténatale; IRM fÅtale; Di George syndrome; 22q11 deletion syndrome; Polyhydramnios; Fetal thymus; Antenatal ultrasound; prenatal MRI;
Early onset intellectual disability in chromosome 22q11.2 deletion syndrome
Keywords: سندرم حذف 22q11; DiGeorge syndrome; Velocardiofacial syndrome; Microdeletion syndrome; 22q11 deletion syndrome; Tetralogy of Fallot; Cognitive impairment; Intellectual disability disordersSíndrome de DiGeorge; Síndrome velocardiofacial; Síndrome de microdeleción; Síndrome
3 generation pedigree with paternal transmission of the 22q11.2 deletion syndrome: Intrafamilial phenotypic variability
Keywords: سندرم حذف 22q11; 22q11 deletion syndrome; Phenotypic variability; Intellectual disability; Adaptive functioning; Paternal transmission
Aberrant Cortical Morphometry in the 22q11.2 Deletion Syndrome
Keywords: سندرم حذف 22q11; 22q11 Deletion syndrome; Cortical thickness; Genetics; Gyrification index; MRI; Psychosis;
Presenting symptoms in adults with the 22q11 deletion syndrome
Keywords: سندرم حذف 22q11; 22q11 Deletion syndrome; Presenting symptoms; Age at diagnosis; Intellectual disability; Psychiatry; Adults
Is child intelligence associated with parent and sibling intelligence in individuals with developmental disorders? An investigation in youth with 22q11.2 deletion (velo-cardio-facial) syndrome
Keywords: سندرم حذف 22q11; Intelligence; Parent-child correlations; Developmental disability; Velo-cardio-facial syndrome; 22q11 deletion syndrome;
SÃndrome de microdeleción 22q11: manifestaciones cardiorrespiratorias y utilidad de la fibrobroncoscopia
Keywords: سندرم حذف 22q11; Microdeleción 22q11; Malformación de la vÃa aérea; Fibrobroncoscopia; 22q11 deletion syndrome; Structural airway anomaly; Fibrobronchoscopy;
Neuroanatomy in adolescents and young adults with 22q11 Deletion Syndrome: Comparison to an IQ-matched group
Keywords: سندرم حذف 22q11; 22q11 deletion syndrome; Velocardiofacial syndrome; Magnetic resonance imaging; Learning disability; Schizophrenia;
22q11 chromosome abnormalities and the cleft service
Keywords: سندرم حذف 22q11; 22q11 deletion syndrome; Velocardiofacial syndrome; DiGeorge syndrome; Cleft palate; Submucous cleft; Velophayngeal insuffiency
The neuropsychology of 22q11 deletion syndrome. A neuropsychiatric study of 100 individuals
Keywords: سندرم حذف 22q11; 22q11 deletion syndrome; Intellectual ability; Executive function; ASD; ADHD
Cognitive and Psychiatric Predictors to Psychosis in Velocardiofacial Syndrome: A 3-Year Follow-Up Study
Keywords: سندرم حذف 22q11; velocardiofacial syndrome (VCFS); 22q11 deletion syndrome; cognition; psychosis; longitudinal;
Autism, ADHD, mental retardation and behavior problems in 100 individuals with 22q11 deletion syndrome
Keywords: سندرم حذف 22q11; 22q11 deletion syndrome; Autism; ADHD; Mental retardation
Prevalence of 22q11.2 deletions in 311 Dutch patients with schizophrenia
Keywords: سندرم حذف 22q11; 22q11 deletion syndrome; 22q11DS; Schizophrenia; VCFS; Deficit syndrome; Prevalence
Structural changes to the fusiform gyrus: A cerebral marker for social impairments in 22q11.2 deletion syndrome?
Keywords: سندرم حذف 22q11; 22q11DS, 22q11.2 deletion syndrome; FG, fusiform gyrus; MRI, magnetic resonance imaging.Velocardiofacial syndrome; 22q11 deletion syndrome; Fusiform gyrus; Structural MRI; Face processing; Psychosis
Catechol-O-methyl Transferase and Expression of Schizophrenia in 73 Adults with 22q11 Deletion Syndrome
Keywords: سندرم حذف 22q11; Catechol-O-methyl transferase; genetic risk; impulsivity; schizophrenia; velocardiofacial syndrome; 22q11 deletion syndrome
Mathematical disabilities in children with velo-cardio-facial syndrome
Keywords: سندرم حذف 22q11; Cognitive phenotype; Number processing; Learning disabilities; Developmental dyscalculia; 22q11 deletion syndrome;
The neuropsychological phenotype of velocardiofacial syndrome (VCFS): Relationship to psychopathology
Keywords: سندرم حذف 22q11; Neuropsychology; Genetics; Velocardiofacial syndrome; 22q11 deletion syndrome; Psychopathology
The 22q11.2 Deletion in Children : High Rate of Autistic Disorders and Early Onset of Psychotic Symptoms
Keywords: سندرم حذف 22q11; 22q11 deletion syndrome; velocardiofacial syndrome; autism; psychosis; behavioral phenotype
Abnormal patterns of cortical gyrification in velo-cardio-facial syndrome (deletion 22q11.2): An MRI study
Keywords: سندرم حذف 22q11; 22q11 deletion syndrome; VCFS; Gyrification index; Schizophrenia; Cortical complexity
Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants
Keywords: سندرم حذف 22q11; Tbx1; Fgf8; 22q11 Deletion syndrome; Cardiovascular development; Genetic interaction; Pharyngeal apparatus; Pharyngeal endoderm
Temporal perception in velo-cardio-facial syndrome
Keywords: سندرم حذف 22q11; Time perception; 22q11 Deletion syndrome; Cerebellum; Caudate nucleus; Fronto-striatal circuit; VCFS; Phenotype;
Loss of Gbx2 results in neural crest cell patterning and pharyngeal arch artery defects in the mouse embryo
Keywords: سندرم حذف 22q11; Cardiovascular; 22q11 deletion syndrome; Pharyngeal arches; Pharyngeal arch arteries; Neural crest; Gbx2; Fgf8; DiGeorge syndrome;