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Items: 5

1.
Mutation rate in the hypervariable VNTR g3 (D7S22) is affected by allele length and a flanking DNA sequence polymorphism near the repeat array.
R. Andreassen, T. Egeland, B. Olaisen
Am J Hum Genet. 1996 Aug; 59(2): 360–367.
PMCID:
PMC1914730
SummaryPage BrowsePDF–1.4M
2.
Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity.
M Muenke, F Gurrieri, C Bay, D H Yi, A L Collins, V P Johnson, R C Hennekam, G B Schaefer, L Weik, M S Lubinsky, et al.
Proc Natl Acad Sci U S A. 1994 Aug 16; 91(17): 8102–8106. doi: 10.1073/pnas.91.17.8102
PMCID:
PMC44553
SummaryPage BrowsePDF–790K
3.
Amplification of human minisatellites by the polymerase chain reaction: towards DNA fingerprinting of single cells.
A J Jeffreys, V Wilson, R Neumann, J Keyte
Nucleic Acids Res. 1988 Dec 9; 16(23): 10953–10971. doi: 10.1093/nar/16.23.10953
PMCID:
PMC338990
SummaryPage BrowsePDF–2.3M
4.
Cloning a selected fragment from a human DNA 'fingerprint': isolation of an extremely polymorphic minisatellite.
Z Wong, V Wilson, A J Jeffreys, S L Thein
Nucleic Acids Res. 1986 Jun 11; 14(11): 4605–4616. doi: 10.1093/nar/14.11.4605
PMCID:
PMC311468
SummaryPage BrowsePDF–1.3M
5.
Recombination initiation maps of individual human genomes
Florencia Pratto, Kevin Brick, Pavel Khil, Fatima Smagulova, Galina V. Petukhova, R. Daniel Camerini-Otero
Science. Author manuscript; available in PMC 2017 Sep 7.
Published in final edited form as: Science. 2014 Nov 14; 346(6211): 1256442. doi: 10.1126/science.1256442
PMCID:
PMC5588152
ArticlePDF–2.7M

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