about
The inv dup (15) or idic (15) syndrome (Tetrasomy 15q)Additional complexity on human chromosome 15q: identification of a set of newly recognized duplicons (LCR15) on 15q11-q13, 15q24, and 15q26.Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14.Hippocampal abnormalities in magnetic resonance imaging (MRI) of 15q duplication syndromes.Inherited DNA amplification of the proximal 15q region: cytogenetic and molecular studies.Triplication of 15q11-q13 with inv dup(15) in a female with developmental delay.Large inv dup(15) chromosome in two generationsHigh-resolution molecular characterization of 15q11-q13 rearrangements by array comparative genomic hybridization (array CGH) with detection of gene dosageChromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints.Two inv dup(15) chromosomes in a woman with repeated abortions.A study of two Chinese patients with tetrasomy and pentasomy 15q11q13 including Prader-Willi/Angelman syndrome critical region present with developmental delays and mental impairment.Inherited interstitial duplications of proximal 15q: genotype-phenotype correlations.Angelman syndrome phenotype associated with mutations in MECP2, a gene encoding a methyl CpG binding proteinMolecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients.The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplicationsPaternal Transmission of Small Supernumerary Marker Chromosome 15 Identified in Prenatal Diagnosis Due to Advanced Maternal Age.Differences between the pattern of developmental abnormalities in autism associated with duplications 15q11.2-q13 and idiopathic autism.Williams Syndrome and 15q Duplication: Coincidence versus Association.Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8, 18, and 21 in three patients.Prenatal diagnosis of partial tetrasomy 14: a case study.Developmental delay caused by a supernumerary chromosome, inv dup (15), identified by fluorescent in situ hybridization.
P2860
Q28301354-CDB79791-5CD2-4881-AE16-970C5D23EED4Q30168524-D9F2001D-6164-44B5-810E-7C9065E0000CQ30495343-993214F4-50EA-4E5F-89CD-4E06CC60B751Q30834483-321A5554-4072-463E-BA2E-BE211FC7E87CQ33678546-C2034B43-8F16-4D69-A77B-EB68A3735A8FQ33680746-AD5C3C43-427E-481E-8B8A-6F288B14F260Q33683424-B29E4ABC-A054-4FBF-8371-B5D03E22AADFQ33998533-285C70C7-C942-479B-8E78-79DF5FEA722AQ34389945-8F6ADD18-BE60-4044-A8CE-C0442F56D0A1Q34468917-4E31A135-E60C-49F2-993E-FD36C0A59EC8Q34548757-4BCB9BB8-F75D-4260-A368-63297B564B65Q35250235-5FAEE017-AA71-4677-ACD1-89C60D3E8B96Q35437213-4D8EAEA0-B6CA-4861-8EB2-65F9FD8D2E41Q35643492-1CF57599-64E0-4768-8AC7-DF8C9F6052E2Q35881781-D8841801-E60E-451F-89C2-9FF86CB0056DQ36212709-D173B0A6-17EE-4E52-B81F-8ABE7C70BE22Q36730353-1A15859C-EF24-47AA-953D-0AB448799EB2Q37603018-718483BB-8E98-407F-81CE-97693484F857Q38462574-4F1CD3F5-8C58-4038-ABBF-C5A28669826CQ48682052-2A6D1834-31E6-4DBF-BBA8-8CDE95B33184Q52209400-1749F1F7-4678-482A-97C9-2182895BB8FC
P2860
description
1994 nî lūn-bûn
@nan
1994 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
Inv dup(15) supernumerary marker chromosomes.
@ast
Inv dup(15) supernumerary marker chromosomes.
@en
type
label
Inv dup(15) supernumerary marker chromosomes.
@ast
Inv dup(15) supernumerary marker chromosomes.
@en
prefLabel
Inv dup(15) supernumerary marker chromosomes.
@ast
Inv dup(15) supernumerary marker chromosomes.
@en
P2860
P356
P1476
Inv dup(15) supernumerary marker chromosomes.
@en
P2093
P2860
P304
P356
10.1136/JMG.31.8.585
P407
P577
1994-08-01T00:00:00Z