Clinical genetic evaluation of the child with mental retardation or developmental delays.
about
Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalitiesConsensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomaliesMultiplex ligation-dependant probe amplification study of children with idiopathic mental retardation in South IndiaSubtelomeric FISH analysis in 76 patients with syndromic developmental delay/intellectual disability.Complex aetiology of an apparently Mendelian form of mental retardation.Submicroscopic subtelomeric aberrations in Chinese patients with unexplained developmental delay/mental retardation.Genetics of autism and mental retardation: A spoonful from the sea!Translating personalized medicine using new genetic technologies in clinical practice: the ethical issuesGenome-wide UPD screening in patients with intellectual disabilityXLMR genes: update 2007.[Neuropsychomotor developmental delay: conceptual map, term definitions, uses and limitations].Caregiver opinions about fragile X population screening.Routine chromosomal microarray analysis is necessary in Korean patients with unexplained developmental delay/mental retardation/autism spectrum disorder.Aetiologic spectrum of mental retardation & developmental delay in India.Physicians' perspectives on the uncertainties and implications of chromosomal microarray testing of children and familiesAbsence of subtelomeric rearrangements in selected patients with mental retardation as assessed by multiprobe T FISH.Multiplex ligation-dependent probe amplification workflow for the detection of submicroscopic chromosomal abnormalities in patients with developmental delay/intellectual disability.Policy considerations in designing a fragile X population screening programTo determine the frequency of subtelomeric abnormalities in children with idiopathic mental retardation.The utility of chromosomal microarray analysis in developmental and behavioral pediatrics.Developmental and behavioral pediatricians' attitudes toward screening for fragile X.Utilization of genetic testing among children with developmental disabilities in the United States.Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia.Dysmorphology at a distance: results of a web-based diagnostic serviceA systematic review of population screening for fragile X syndrome.Compendium of national guidelines for imaging of the pediatric patient.Unexplained developmental delay/learning disability: guidelines for best practice protocol for first line assessment and genetic/metabolic/radiological investigations.Genetic testing in patients with global developmental delay / intellectual disabilities. A review.Dysmorphology services: a snapshot of current practices and a vision for the future.Implementation of an electronic genomic and family health history tool in primary prenatal care.Sex Education and Intellectual Disability: Practices and Insight from Pediatric Genetic Counselors.Detailed assessment of incontinence in boys with fragile-X-syndrome in a home setting.Identifying the KAT6B Mutation via Diagnostic Exome Sequencing to Diagnose Say-Barber-Biesecker-Young-Simpson Syndrome in Three Generations of a FamilyAetiology of intellectual disability in paediatric outpatients in Northern India.The clinical utility of MRI in patients with neurodevelopmental disorders of unknown origin.Spectrum of neurodevelopmental disabilities: a cohort study in hungary.High prevalence of array comparative genomic hybridization abnormalities in adults with unexplained intellectual disability.Practice parameters in child neurology: do pediatricians use them?Low-Functioning Autism and Nonsyndromic Intellectual Disability: Magnetic Resonance Imaging (MRI) Findings.Cortical maturation in fetuses referred for 'isolated' mild ventriculomegaly: a longitudinal ultrasound assessment.
P2860
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P2860
Clinical genetic evaluation of the child with mental retardation or developmental delays.
description
2006 nî lūn-bûn
@nan
2006 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Clinical genetic evaluation of the child with mental retardation or developmental delays.
@ast
Clinical genetic evaluation of the child with mental retardation or developmental delays.
@en
type
label
Clinical genetic evaluation of the child with mental retardation or developmental delays.
@ast
Clinical genetic evaluation of the child with mental retardation or developmental delays.
@en
prefLabel
Clinical genetic evaluation of the child with mental retardation or developmental delays.
@ast
Clinical genetic evaluation of the child with mental retardation or developmental delays.
@en
P2093
P356
P1433
P1476
Clinical genetic evaluation of the child with mental retardation or developmental delays.
@en
P2093
American Academy of Pediatrics Committee on Genetics
John B Moeschler
Michael Shevell
P304
P356
10.1542/PEDS.2006-1006
P407
P577
2006-06-01T00:00:00Z