[go: up one dir, main page]

Streata et al., 2020 - Google Patents

Phenotype heterogeneity in 3q29 microduplication syndrome

Streata et al., 2020

View HTML
Document ID
4200282263911368199
Author
Streata I
Riza A
Sosoi S
Burada F
Ioana M
Publication year
Publication venue
Current Health Sciences Journal

External Links

Snippet

3q29 microduplication syndrome is characterized by widely variable clinical presentation, but generally mild features. Developmental delay, particularly speech, and intellectual disability, eye abnormalities and heart defects are more frequently seen in affected …
Continue reading at pmc.ncbi.nlm.nih.gov (HTML) (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES OR MICRO-ORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6876Hybridisation probes
    • C12Q1/6883Hybridisation probes for diseases caused by alterations of genetic material
    • GPHYSICS
    • G06COMPUTING; CALCULATING; COUNTING
    • G06FELECTRICAL DIGITAL DATA PROCESSING
    • G06F19/00Digital computing or data processing equipment or methods, specially adapted for specific applications
    • G06F19/30Medical informatics, i.e. computer-based analysis or dissemination of patient or disease data
    • G06F19/34Computer-assisted medical diagnosis or treatment, e.g. computerised prescription or delivery of medication or diets, computerised local control of medical devices, medical expert systems or telemedicine
    • G06F19/345Medical expert systems, neural networks or other automated diagnosis
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES OR MICRO-ORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q2600/00Oligonucleotides characterized by their use
    • C12Q2600/156Polymorphic or mutational markers

Similar Documents

Publication Publication Date Title
Bureau et al. Epileptic syndromes in infancy, childhood and adolescence
Fang et al. Artificial intelligence framework identifies candidate targets for drug repurposing in Alzheimer’s disease
Hardiman et al. Amyotrophic lateral sclerosis
Walhovd et al. Timing of lifespan influences on brain and cognition
Salameh et al. Amyotrophic lateral sclerosis
De La Torre-Ubieta et al. Advancing the understanding of autism disease mechanisms through genetics
Oskoui et al. Clinically relevant copy number variations detected in cerebral palsy
Castronovo et al. Phenotypic spectrum of NRXN1 mono‐and bi‐allelic deficiency: a systematic review
Korvatska et al. R47H variant of TREM2 associated with Alzheimer disease in a large late-onset family: clinical, genetic, and neuropathological study
Parisi Clinical and molecular features of Joubert syndrome and related disorders
WO2018077303A1 (en) Compositions, methods and kits for detection of genetic variants for alzheimer's disease
van Eyk et al. Redefining cerebral palsies as a diverse group of neurodevelopmental disorders with genetic aetiology
Celestino-Soper et al. Deletions in chromosome 6p22. 3-p24. 3, including ATXN1, are associated with developmental delay and autism spectrum disorders
Micalizzi et al. Clinical, neuroradiological and molecular characterization of cerebellar dysplasia with cysts (Poretti–Boltshauser syndrome)
Elkaim et al. Deep brain stimulation for childhood dystonia: current evidence and emerging practice
Nho et al. Integration of bioinformatics and imaging informatics for identifying rare PSEN1 variants in Alzheimer’s disease
Fowler et al. Leveraging existing data sets to generate new insights into Alzheimer’s disease biology in specific patient subsets
Ramanan et al. Variants in PPP2R2B and IGF2BP3 are associated with higher tau deposition
Liu et al. The association between TOMM40 gene polymorphism and spontaneous brain activity in amnestic mild cognitive impairment
Bonham et al. Radiogenomics of C9orf72 expansion carriers reveals global transposable element derepression and enables prediction of thalamic atrophy and clinical impairment
Lu et al. Identification of a de novo mutation of the FOXG1 gene and comprehensive analysis for molecular factors in Chinese FOXG1-related encephalopathies
Streata et al. Phenotype heterogeneity in 3q29 microduplication syndrome
Madrigal et al. Spectrum of clinical heterogeneity of β-tubulin TUBB5 gene mutations
Roussotte et al. Neuroimaging and genetic risk for Alzheimer’s disease and addiction-related degenerative brain disorders
Manca et al. The neural signatures of psychoses in Alzheimer’s disease: a neuroimaging genetics approach