2008
Molecular characterization of a patient with 3p deletion syndrome and a review of the literature
Fernandez TV, García‐González I, Mason CE, Hernández‐Zaragoza G, Ledezma‐Rodríguez V, Anguiano‐Alvarez V, E'Vega R, Gutiérrez‐Angulo M, Maya ML, García‐Bejarano H, González‐Cruz M, Barrios S, Atorga R, López‐Cardona M, Armendariz‐Borunda J, State MW, Dávalos NO. Molecular characterization of a patient with 3p deletion syndrome and a review of the literature. American Journal Of Medical Genetics Part A 2008, 146A: 2746-2752. PMID: 18837054, DOI: 10.1002/ajmg.a.32533.Peer-Reviewed Original ResearchMeSH KeywordsChild, PreschoolChromosome DeletionChromosome DisordersChromosomes, Human, Pair 13Chromosomes, Human, Pair 3Comparative Genomic HybridizationCraniofacial AbnormalitiesDevelopmental DisabilitiesFemaleHumansIn Situ Hybridization, FluorescenceKaryotypingLimb Deformities, CongenitalMalePhenotypeSyndromeTranslocation, GeneticConceptsDeletion syndromeDysmorphic physical featuresArray-based comparative genomic hybridizationChild patientsRare disorderNovo unbalanced translocationGrowth retardationSyndromeDevelopmental delayRoutine cytogenetic analysisUnbalanced abnormalitiesComparative genomic hybridizationChromosome 3p26Unbalanced translocationPatientsChromosome 3pMb deletionCytogenetic analysisDisordersRare chromosomal rearrangementsSitu hybridizationGenomic hybridizationMb terminal deletionTerminal deletionDisruption of Contactin 4 (CNTN4) Results in Developmental Delay and Other Features of 3p Deletion Syndrome
Fernandez T, Morgan T, Davis N, Klin A, Morris A, Farhi A, Lifton RP, State MW. Disruption of Contactin 4 (CNTN4) Results in Developmental Delay and Other Features of 3p Deletion Syndrome. American Journal Of Human Genetics 2008, 82: 1385. PMID: 18551756, PMCID: PMC2661627, DOI: 10.1016/j.ajhg.2008.04.021.Peer-Reviewed Original Research
2004
Disruption of Contactin 4 (CNTN4) Results in Developmental Delay and Other Features of 3p Deletion Syndrome
Fernandez T, Morgan T, Davis N, Klin A, Morris A, Farhi A, Lifton RP, State MW. Disruption of Contactin 4 (CNTN4) Results in Developmental Delay and Other Features of 3p Deletion Syndrome. American Journal Of Human Genetics 2004, 74: 1286-1293. PMID: 15106122, PMCID: PMC1182094, DOI: 10.1086/421474.Peer-Reviewed Original ResearchMeSH KeywordsCell Adhesion Molecules, NeuronalChildChromosome BreakageChromosome DeletionChromosomes, Human, Pair 10Chromosomes, Human, Pair 3ContactinsCraniofacial AbnormalitiesDevelopmental DisabilitiesGene RearrangementGrowth DisordersHumansIn Situ Hybridization, FluorescenceKaryotypingMalePhenotypeRNA, MessengerSyndromeTelomereTranslocation, GeneticConceptsCentral nervous systemDevelopmental delayDeletion syndromeObserved clinical manifestationsAbnormal CNS developmentNeuronal cell adhesion moleculeClinical manifestationsCell adhesion moleculeNervous systemCharacteristic physical featuresGrowth retardationSyndromeDeletion syndrome phenotypeDysmorphic featuresAxon growthContiguous gene disorderImmunoglobulin super familyAdhesion moleculesSyndrome phenotypeCausative relationshipCNS developmentNeural developmentTelomeric portionRare contiguous gene disorderChromosome 3
1999
Clinical and Neurobiological Correlates of Cytogenetic Abnormalities in Childhood-Onset Schizophrenia
Nicolson R, Giedd JN, Lenane M, Hamburger S, Singaracharlu S, Bedwell J, Fernandez T, Thaker GK, Malaspina D, Rapoport JL. Clinical and Neurobiological Correlates of Cytogenetic Abnormalities in Childhood-Onset Schizophrenia. American Journal Of Psychiatry 1999, 156: 1575-1579. PMID: 10518169, DOI: 10.1176/ajp.156.10.1575.Peer-Reviewed Original ResearchMeSH KeywordsAdolescentAge of OnsetBrainBrief Psychiatric Rating ScaleCerebral VentriclesChildChromosome AberrationsChromosome DeletionDevelopmental DisabilitiesFamilyFemaleHippocampusHumansIntelligence TestsMagnetic Resonance ImagingMalePrevalencePsychiatric Status Rating ScalesRisk FactorsSchizophreniaSchizophrenic PsychologyConceptsChildhood-onset schizophreniaCytogenetic abnormalitiesCytogenetic anomaliesEye tracking dysfunctionSubgroup of patientsChromosome 22q11 deletionNeurobiological correlatesRisk factor measuresSchizophrenia spectrum disordersObstetric complicationsGroup of childrenEtiologic contributionPathophysiologic roleChildhood onsetFragile X testingLower performance IQPatientsGreater impairmentAbnormalitiesDevelopmental impairmentEarly onsetChromosomal abnormalitiesSchizophreniaEarly ageImpairment