STS for Minisatellite MS607 (D22S163)

Overview

Journal Nucleic Acids Res

Publisher Oxford University Press

Specialty Biochemistry

Date 1991 Jun 11

PMID 2057375

Citations 4

Authors

J A Armour

A J Jeffreys

Affiliations

Soon will be listed here.

Citing Articles

Identification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome.

Bonaglia M, Giorda R, Mani E, Aceti G, Anderlid B, Baroncini A J Med Genet. 2005; 43(10):822-8.

PMID: 16284256 PMC: 2563164. DOI: 10.1136/jmg.2005.038604.

Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms.

Wilson H, Wong A, Shaw S, Tse W, Stapleton G, Phelan M J Med Genet. 2003; 40(8):575-84.

PMID: 12920066 PMC: 1735560. DOI: 10.1136/jmg.40.8.575.

Molecular characterization of a 130-kb terminal microdeletion at 22q in a child with mild mental retardation.

Wong A, Ning Y, Flint J, Clark K, Dumanski J, Ledbetter D Am J Hum Genet. 1997; 60(1):113-20.

PMID: 8981954 PMC: 1712560.

New nucleotide sequence data on the EMBL File Server.

Nucleic Acids Res. 1991; 19(21):6063-79.

PMID: 1945897 PMC: 329084. DOI: 10.1093/nar/19.21.6063.

References

Jeffreys A, Wilson V, Neumann R, Keyte J . Amplification of human minisatellites by the polymerase chain reaction: towards DNA fingerprinting of single cells. Nucleic Acids Res. 1988; 16(23):10953-71. PMC: 338990. DOI: 10.1093/nar/16.23.10953. View

Armour J, Povey S, Jeremiah S, Jeffreys A . Systematic cloning of human minisatellites from ordered array charomid libraries. Genomics. 1990; 8(3):501-12. DOI: 10.1016/0888-7543(90)90037-u. View

Jeffreys A, Neumann R, Wilson V . Repeat unit sequence variation in minisatellites: a novel source of DNA polymorphism for studying variation and mutation by single molecule analysis. Cell. 1990; 60(3):473-85. DOI: 10.1016/0092-8674(90)90598-9. View