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City Minneapolis / Sanlaville / Shevell / / Company Ravan SA / GE / Chudley AE / Humans Using Ensembl Resources / / Country United States / / Currency pence / / / Facility American College of Medical Genetics / University of Arkansas / / IndustryTerm magnetic resonance imaging / routine magnetic resonance imaging / quality medical services / Array-based technology / helpful diagnostic tool / clinical testing technology / advance online publication / array technology / / MedicalCondition microcephaly / tremors / specific disorder / autistic spectrum disorders / JE / acidosis / untreated phenylketonuria / seizures / syndromic and non-syndromic autism / Smith-Magenis syndrome / Another disorder / developmental disabilities / novel autism / Sanfilippo syndrome / dysfunction / Coleman M. Autism / Fryns syndrome / apparent neurobehavioral disorders / mitochondrial disorders / alopecia / syndrome MED12 disorders / unexplained autism / electrolyte disturbances Anemia / autism spectrum disorder / metabolism Disorders / Cowden syndrome / X syndrome / X-linked neurodevelopmental disorders / febrile illness / learning disabilities / recurrent respiratory infections / MeCP2 duplication syndrome / fragile-X syndrome / relative’s disorder / phenylketonuria / Metabolic disorders / illness / MS / attention-deficit hyperactivity disorder / infantile autism / developmental delays/mental retardation / pervasive developmental disorder / Asperger syndrome / Neurometabolic disorders / neurologic symptoms / Mental Disorders / pervasive developmental disorders / Attention-deficit/hyperactivity disorder / Rett syndrome / ataxia / autism spectrum disorders / neurodevelopmental disorders / mitochondrial dysfunction / succinic semialdehyde dehydrogenase deficiency / parkinsonism / atypical autism / Fombonne E. Pervasive developmental disorders / spectrum disorder / Willi syndrome PTEN-associated disorders / Ruvalcaba syndrome / mitochondrial disease / nucleotidase superactivity Dihydropyrimidinase deficiency Disorders / autism / tumour / autistic disorder / Mild Sanfilippo syndrome / lethargy / genetic and genomic disorders / mitochondrial disorder / drooling / significant hearing loss / affective disorder / movement disorders / Gastrointestinal dysfunction / single-gene disorders / syndromic autism spectrum disorders / nonsyndromic autistic disorder / hypertrichosis / Seizures ASD / hypotonia / stupor/coma / dystonia / inborn errors of metabolism / deficiency / Opitz syndrome / neurodevelopmental and neurobehavioral disorders / spectrum disorders / disorders / classic Rett syndrome / Sotos syndrome / / MedicalTreatment immunization / counseling / / NaturalFeature Stein MT / Acosta MT / Pastore MT / / OperatingSystem Xp / / Organization American College of Medical Genetics / Society for Inherited Metabolic Disorders / University of Arkansas / ASDs.69 This / Department of Genetics and Pediatrics / Professional Practice and Guidelines Committee / Strong / / Person Ann Neurol / Reynolds A. Autistic / Mayo Clin Proc / Clin Pediatr / G. Bradley Schaefer / Marshall A. Childhood / Nancy J. Mendelsohn / / Position Prime Minister / care physician / metabolic specialist / RT / Butler / Adam MP / geneticist and genetic counselor / / ProvinceOrState Minnesota / South Dakota / Manitoba / Arkansas / / PublishedMedium PLoS ONE / / RadioStation Am 2010 / Abbacchi AM / / Technology Genomics / Bioinformatics / diagnostic tests / hybridization / array technology / Human Genome / MRI / Array-based technology / magnetic resonance imaging / clinical testing technology / DNA Chip / spectroscopy / / URL http / SocialTag 
© American College of Medical Genetics and Genomics ACMG Practice Guidelines Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions