A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man
about
Mosaic supernumerary ring chromosome 19 identified by comparative genomic hybridisationMolecular cytogenetic characterisation of a small ring X chromosome in a Turner patient and in a male patient with congenital abnormalities: role of X inactivationA review of fluorescence in situ hybridization (FISH): current status and future prospects.Prenatal diagnosis of a de novo supernumerary marker derived from chromosome 16.A functional marker centromere with no detectable alpha-satellite, satellite III, or CENP-B protein: activation of a latent centromere?Characterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH).Centromere DNA dynamics: latent centromeres and neocentromere formation.Identification of supernumerary marker chromosomes derived from chromosomes 5, 6, 19, and 20 using FISH.Tetrasomy 15q: two marker chromosomes with no detectable alpha-satellite DNAA stable acentric marker chromosome: possible existence of an intercalary ancient centromere at distal 8pGeneration of a human X-derived minichromosome using telomere-associated chromosome fragmentation.A new small supernumerary marker chromosome, generating mosaic pure trisomy 16q11.1-q12.1 in a healthy man.An apparently acentric marker chromosome originating from 9p with a functional centromere without detectable alpha and beta satellite sequences.A molecular and FISH approach to determining karyotype and phenotype correlations in six patients with supernumerary marker(22) chromosomes.Neocentromere at 13q32 in one of two stable markers derived from a 13q21 break.Prenatal diagnosis of partial tetrasomy 14: a case study.Mosaic tetrasomy 15q25-->qter in a newborn infant with multiple anomalies.Developmental delay caused by a supernumerary chromosome, inv dup (15), identified by fluorescent in situ hybridization.Tetrasomy 15q25.2→qter identified with SNP microarray in a patient with multiple anomalies including complex cardiovascular malformation.
P2860
Q31995052-8484C0C6-66D8-4003-B642-F2B6A89FBABDQ33675752-14EA8E70-1242-46C0-AF8F-354FEF80379BQ34002217-8E33897A-FE15-4662-A4C9-270DB16D4EA9Q34299793-88E6AACD-B314-4A9E-9A8B-4BC16623E70DQ35194698-D9A01432-2C09-451A-B27B-08D7BEA0D57DQ35194867-72501822-E5D0-462E-8761-ECC448ECC4E1Q35250147-1E01C358-E926-4585-93FA-5D63E33ED379Q35434123-21E26AE0-2253-4710-901B-182DA06DD3BEQ35889346-B5DF0591-6F4D-4C07-9838-87D29B5507E2Q35889830-B480AA0A-4B00-40DA-A7F6-FD7F703B0D5BQ37624580-59C18D0A-A554-4DB6-B550-5978779A0CB3Q38286655-4DAD67D6-3153-4AD4-9E11-3E53C2227712Q38504030-9CF5A6B6-0B23-4E6E-88DA-7855F66552F3Q41074063-DE925D79-EE8F-4D9A-BAC8-6A823C017BE6Q41925663-E33332FC-F2BA-45E2-B117-FA9EA17E9CF4Q48682052-B440A81F-0904-4BD5-8FD6-79C60B241538Q49167099-7696F47F-231F-4E05-B97A-18578BDB678BQ52209400-79AD61B0-1E85-4B32-9464-EBCF774616BEQ53161929-03CE4259-A9FB-449B-8B55-58B394DB6828
P2860
A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man
description
1992 nî lūn-bûn
@nan
1992 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
A non-isotopic in situ hybridi ...... rary marker chromosomes in man
@ast
A non-isotopic in situ hybridi ...... rary marker chromosomes in man
@en
type
label
A non-isotopic in situ hybridi ...... rary marker chromosomes in man
@ast
A non-isotopic in situ hybridi ...... rary marker chromosomes in man
@en
prefLabel
A non-isotopic in situ hybridi ...... rary marker chromosomes in man
@ast
A non-isotopic in situ hybridi ...... rary marker chromosomes in man
@en
P2093
P2860
P356
P1476
A non-isotopic in situ hybridi ...... rary marker chromosomes in man
@en
P2093
P2860
P304
P356
10.1136/JMG.29.10.699
P407
P577
1992-10-01T00:00:00Z