The inv dup(15) syndrome: a clinically recognizable syndrome with altered behavior, mental retardation, and epilepsy.
about
Multiple forms of atypical rearrangements generating supernumerary derivative chromosome 15The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13Chromosome imbalances associated with epilepsyThe inv dup (15) or idic (15) syndrome (Tetrasomy 15q)Clinical review of genetic epileptic encephalopathiesHippocampal abnormalities in magnetic resonance imaging (MRI) of 15q duplication syndromes.Recent advances in the genetics of epilepsy: insights from human and animal studies.Three probands with autistic disorder and isodicentric chromosome 15.Rearrangements of chromosome 15 in epilepsy.Diagnostic evaluation of developmental delay/mental retardation: An overview.Origins of accessory small ring marker chromosomes derived from chromosome 1.A case of isodicentric chromosome 15 presented with epilepsy and developmental delayIdentification of a distinct developmental and behavioral profile in children with Dup15q syndromeGenetic evaluation and counseling for epilepsy.Emotion-induced myoclonic absence-like seizures in a patient with inv-dup(15) syndrome: a clinical, EEG, and molecular genetic study.Spectrum of epilepsy and electroencephalogram patterns in Wolf-Hirschhorn syndrome: experience with 87 patients.Prenatal Diagnosis of Mosaic Tetrasomy 18p in a Case without Sonographic AbnormalitiesCommon Regulatory Variants of CYFIP1 Contribute to Susceptibility for Autism Spectrum Disorder (ASD) and Classical Autism.Three supernumerary marker chromosomes in a patient with developmental delay, mental retardation, and dysmorphic features.Autistic disorder associated with a paternally derived unbalanced translocation leading to duplication of chromosome 15pter-q13.2: a case report.Pervasive developmental disorders and GABAergic system in patients with inverted duplicated chromosome 15.Mild generalized epilepsy and developmental disorder associated with large inv dup(15).Spectrum of epilepsy in terminal 1p36 deletion syndrome.Association analysis of chromosome 15 gabaa receptor subunit genes in autistic disorder.The yield of subtelomeric FISH analysis in the evaluation of autistic spectrum disorders.The behavioral phenotype of the idic(15) syndrome.Autism and maternally derived aberrations of chromosome 15q.Autism in Angelman syndrome: implications for autism research.A longitudinal follow-up study of autistic symptoms in children and adults with duplications of 15q11-13.The syndrome of inv dup (15): clinical, electroencephalographic, and imaging findings.A survey of seizures and current treatments in 15q duplication syndrome.Epilepsy and electroencephalographic findings in pericentric inversion of chromosome 12.Supernumerary marker chromosomes derived from chromosome 15: analysis of 32 new cases.Usefulness of high-resolution comparative genomic hybridization (CGH) for detecting and characterizing constitutional chromosome abnormalities.Diagnostic yield of the comprehensive assessment of developmental delay/mental retardation in an institute of child neuropsychiatry.Maternally derived 15q11.2-q13.1 duplication in a child with Lennox-Gastaut-type epilepsy and dysmorphic features: Clinical-genetic characterization of the family and review of the literature.Spectrum of epilepsy and electroencephalogram patterns in idic (15) syndrome.Small supernumerary marker chromosome 15 and a ring chromosome 15 associated with a 15q26.3 deletion excluding the IGF1R gene.
P2860
Q21283782-9BABCE22-0D5A-4875-8298-A8748AF584F1Q24594577-C4E447DA-A7C6-4F2D-8A40-6F7EDAFF73CBQ28189593-4933890E-7943-4CFA-B6CD-84EB9C067101Q28301354-C04E7C7C-E21E-442E-BD05-FE25DAE62F2DQ30537230-8A6CF3C0-8160-429D-BDAE-AA9CAD040574Q30834483-0412ABBD-5B4A-4556-912D-5A3C44ECE373Q33755692-D7C0B9BF-3109-4354-8E3C-4A9617156B80Q33970872-CA11C083-9CF5-4C0C-8766-767A87202822Q34386784-8432B1CB-AEB4-402C-93C0-F3FE6431F49AQ35057630-A5C098A7-AA1F-4608-ABBF-9CB07CE55106Q35430951-E4602455-BA16-456E-909C-3372B504829EQ36499665-6530F082-1253-4A1B-8163-91E5D0077D27Q36876026-B482BBA4-BA69-4B83-9352-5BC92575858BQ37774544-7D715DB9-8A32-41BB-97F5-77D6AFEC5D4CQ38554453-F706738F-1CA5-418E-8CBA-D32CFFA9E7FCQ40391962-847B7559-5DC9-4B5E-802E-98F84A66D1F2Q40502014-A55D0AA2-34DA-4046-9A57-45DDE3B289A0Q40816230-25D0F53B-ADF1-4228-9546-D75261E1BEEBQ41809824-6048C011-A698-457B-8D4E-0E9702F9E1ABQ41956312-DB24D991-F3EE-4BE2-BDEC-ECBF7D369942Q43850516-7DBEB700-4A03-49D2-A657-B98C750B13DEQ44117283-2F5D5EC4-3472-424D-A205-1FCAA9CF3F47Q48450753-022295A2-9717-4F19-9672-B0034C8E3F22Q48563558-100742FC-F35F-4D44-B40A-F5B65D786138Q48684336-8A39901A-E4A5-4DD4-930F-821643D0267AQ50301670-7686BC62-FC6D-412F-8277-6389E5F3C530Q50302069-11604E26-BB77-47E3-B7D6-5233FEF2BCE2Q50307340-C1C9EA6E-EDD3-4A49-B988-4B9B8734BE9FQ50307457-7CEA687D-0CC9-41D6-B0D4-A61311F943D8Q50312781-634F421C-1461-4F17-84E3-782EA34939E2Q50343349-1580B687-7678-42CB-9F06-D2164855E0A7Q51934642-2C44203E-59E6-43CA-9328-290AC89CAC0CQ51955271-4B386ACC-8C4B-453B-AACA-C6D7F2C7D3C4Q52113040-861C32DE-1F33-457C-BF7B-AE8C991349A8Q52180232-CBF34068-FB77-4508-BBBA-AAB3F00DB08DQ52959204-02F04E0B-5DDA-4D44-A370-9DA3295D83D7Q53038576-F549D744-A639-4808-817D-9A9421840E18Q53489608-7C2B0FA1-9F38-4229-8E45-38B6625F93BA
P2860
The inv dup(15) syndrome: a clinically recognizable syndrome with altered behavior, mental retardation, and epilepsy.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年学术文章
@wuu
1997年学术文章
@zh
1997年学术文章
@zh-cn
1997年学术文章
@zh-hans
1997年学术文章
@zh-my
1997年学术文章
@zh-sg
1997年學術文章
@yue
1997年學術文章
@zh-hant
name
The inv dup(15) syndrome: a cl ...... tal retardation, and epilepsy.
@en
The inv dup(15) syndrome: a cl ...... tal retardation, and epilepsy.
@nl
type
label
The inv dup(15) syndrome: a cl ...... tal retardation, and epilepsy.
@en
The inv dup(15) syndrome: a cl ...... tal retardation, and epilepsy.
@nl
prefLabel
The inv dup(15) syndrome: a cl ...... tal retardation, and epilepsy.
@en
The inv dup(15) syndrome: a cl ...... tal retardation, and epilepsy.
@nl
P2093
P356
P1433
P1476
The inv dup(15) syndrome: a cl ...... ntal retardation, and epilepsy
@en
P2093
A Battaglia
A Bellacosa
F Gurrieri
M Paravatou-Petsotas
P304
P356
10.1212/WNL.48.4.1081
P407
P577
1997-04-01T00:00:00Z