About: Complex gene conversion events in germline mutation at human minisatellites

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description	article (en) wetenschappelijk artikel (nl) наукова стаття, опублікована в лютому 1994 (uk) article scientifique publié en 1994 (fr) im Februar 1994 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q58992797-E0958D00-DA40-4256-A5D8-401C692CCE81
publication date	1994-02-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q58992797-1A3EE425-AB2E-4461-81BA-AAC3D52AD6F8
language of work or name	English
exact match	wds:Q58992797-6AB8114D-6062-46E1-B101-2EA63EC142BF
exact match	https://scigraph.springernature.com/pub.10.1038/ng0294-136
cites work	wds:Q58992797-03FD5829-5769-4E84-A862-EABB51662B37 wds:Q58992797-0AB0DCE4-BC60-4E8B-8621-D6EC8C6145C8 wds:Q58992797-18920688-48BF-4606-875F-861601903E58 wds:Q58992797-1AC2B629-921F-46DD-8514-6AB0EEEAD952 wds:Q58992797-25424088-DBE2-4D5D-AB63-ABC76BD392E3 wds:Q58992797-5665FC81-8E21-4060-BDE5-A4BA2573CDA6 wds:Q58992797-56AB2595-D3F5-4291-B087-6365F1935D82 wds:Q58992797-5AE97297-334B-4458-BECD-0B25EE2371C6 wds:Q58992797-5C23271C-9A93-4BB8-91DF-2AEB6D9DF037 wds:Q58992797-5F50B1FC-A47E-4D8A-829C-8D49547B3197 wds:Q58992797-653BB592-4536-48A1-AD22-C92F74EBC91A wds:Q58992797-68A4B855-B67D-4014-A74F-857B65CD8C99 wds:Q58992797-79832F9C-CC63-4F2A-B622-580EA3AD4FD0 wds:Q58992797-8A872833-1160-4ED8-A391-4B9684461EE1 wds:Q58992797-A4256E13-ABBC-4E65-BE84-5A9E71B04CF6 wds:Q58992797-A8B49948-1473-4BB0-A927-5793AB014A14 wds:Q58992797-AC9E5EC8-30A4-4066-A39D-E70950759654 wds:Q58992797-C0D74D13-C4F3-4A79-90D8-2478F28DAFD1 wds:Q58992797-CCA76B82-CD5D-41D8-AA4E-AF26CE2A4520 wds:Q58992797-CCBAC305-E231-4719-B441-6F75215B8BF8 wds:Q58992797-D9C7E7AE-DD10-49CA-97C1-3755DDF77A52 wds:Q58992797-E4EFDA49-EFD3-430E-8084-7E8DEDB084C1 wds:Q58992797-F1777CE2-D1A7-4CF1-90BF-3939D7437369 wds:Q58992797-FD128B24-DB82-4548-A5D0-0BAAF2FFBFD7 wds:Q58992797-FF861F6C-FD98-4233-8A23-DE803351C5C2
cites work	Minisatellite repeat coding as a digital approach to DNA typing Repeat unit sequence variation in minisatellites: a novel source of DNA polymorphism for studying variation and mutation by single molecule analysis Characterization of a panel of highly variable minisatellites cloned from human DNA A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Gene conversion, recombination nodules, and the initiation of meiotic synapsis Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation. Association of fragile X syndrome with delayed replication of the FMR1 gene Clustering of hypervariable minisatellites in the proterminal regions of human autosomes The use of synthetic tandem repeats to isolate new VNTR loci: cloning of a human hypermutable sequence Sequences flanking the repeat arrays of human minisatellites: association with tandem and dispersed repeat elements. Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA. Triplet repeat mutations in human disease A poly(dA.dT) tract is a component of the recombination initiation site at the ARG4 locus in Saccharomyces cerevisiae Unequal crossingover between homologous chromosomes is not the major mechanism involved in the generation of new alleles at VNTR loci Allelic diversity at minisatellite MS205 (D16S309): evidence for polarized variability Biology and applications of human minisatellite loci Molecular characterization of a spontaneously generated new allele at a VNTR locus: no exchange of flanking DNA sequence Digital DNA typing at a second hypervariable locus by minisatellite variant repeat mapping A hypervariable locus D16S309 located at the distal end of 16p. Allele-specific MVR-PCR analysis at minisatellite D1S8. Evolutionary transience of hypervariable minisatellites in man and the primates Four-state MVR-PCR: increased discrimination of digital DNA typing by simultaneous analysis of two polymorphic sites within minisatellite variant repeats at D1S8. Minisatellite “isoallele” discrimination in pseudohomozygotes by single molecule PCR and variant repeat mapping DNA-minisatellite mutations: recent investigations concerning distribution and impact on parentage testing
author name string	wds:Q58992797-13D5A140-692A-4485-8560-8E3D31786CE7 wds:Q58992797-4EB9BAFD-86AE-4CE8-B848-EED21E81C6A2 wds:Q58992797-618BD97F-2D66-45F9-971A-A89C32461046 wds:Q58992797-ABAAE9D0-ED2F-4A98-BC96-BB22B4A801C0
author name string	Jeffreys AJ Tamaki K MacLeod A Neil DL
rdfs:label	Complex gene conversion events in germline mutation at human minisatellites (en) Complex gene conversion events in germline mutation at human minisatellites (nl)
skos:prefLabel	Complex gene conversion events in germline mutation at human minisatellites (en) Complex gene conversion events in germline mutation at human minisatellites (nl)
name	Complex gene conversion events in germline mutation at human minisatellites (en) Complex gene conversion events in germline mutation at human minisatellites (nl)
author	wds:Q58992797-C5B200C8-E01B-452F-8C34-7714D57F223E wds:Q58992797-DD8E947F-B61E-48FD-9F10-7C97135A11B7
author	Darren G Monckton John A.L. Armour
title	wds:Q58992797-388407C6-9350-4D4D-8ED4-23D1CB13FDFF
title	Complex gene conversion events in germline mutation at human minisatellites (en)
page(s)	wds:Q58992797-0F9DA83D-1587-4C59-BB58-AE39ED7BF14C
page(s)	136-145
instance of	wds:Q58992797-0687FFB9-D91A-43D5-8DEA-D224474142FD
instance of	scholarly article
PubMed ID	wds:Q58992797-81496692-D06F-4FDE-926D-D9061C592BCA
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/8162067
PubMed ID	8162067
published in	wds:Q58992797-8D54B55C-87BC-41AA-8006-877FECFFB559
published in	Nature Genetics
issue	wds:Q58992797-CEEEC998-E4E6-4475-9B4D-6E9664906582
volume	wds:Q58992797-F6DDAA1A-1F42-4317-80E2-D05E8816871F
issue	2
volume	6
DOI	wds:Q58992797-70F98385-8857-428A-A345-476BE1785589
DOI	http://dx.doi.org/10.1038/NG0294-136
DOI	10.1038/NG0294-136
Fatcat ID	wds:Q58992797-A90C7AD4-BE28-4C2C-9392-E82D010A4FE6
Fatcat ID	release_vmxcpahsafh7vgxfr443sqaqk4

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