A computer program to make linkage analysis with LIPED and LINKAGE easier to perform and less prone to input errors - PubMed (original) (raw)
A computer program to make linkage analysis with LIPED and LINKAGE easier to perform and less prone to input errors
J Attwood et al. Ann Hum Genet. 1988 Jul.
No abstract available
Similar articles
- RI Manager, a microcomputer program for analysis of data from recombinant inbred strains.
Manly KF, Elliott RW. Manly KF, et al. Mamm Genome. 1991;1(2):123-6. doi: 10.1007/BF02443789. Mamm Genome. 1991. PMID: 1799788 - LIPIN: an interactive data entry and management program for LIPED.
Trofatter JA, Haines JL, Conneally PM. Trofatter JA, et al. Am J Hum Genet. 1986 Jul;39(1):147-8. Am J Hum Genet. 1986. PMID: 3755866 Free PMC article. No abstract available. - A simple method to detect linkage for rare recessive diseases: an application to juvenile diabetes.
Suarez BK, Hodge SE. Suarez BK, et al. Clin Genet. 1979 Feb;15(2):126-36. doi: 10.1111/j.1399-0004.1979.tb01751.x. Clin Genet. 1979. PMID: 367641 - Use of LINKAGE programs for linkage analysis.
Speer MC. Speer MC. Curr Protoc Hum Genet. 2006 Feb;Chapter 1:Unit 1.7. doi: 10.1002/0471142905.hg0107s48. Curr Protoc Hum Genet. 2006. PMID: 18428385 Review. - Software for genetic linkage analysis: an update.
Bryant SP. Bryant SP. Mol Biotechnol. 1996 Feb;5(1):49-61. doi: 10.1007/BF02762412. Mol Biotechnol. 1996. PMID: 8853016 Review.
Cited by
- Evidence for genetic heterogeneity in tuberous sclerosis.
Sampson JR, Yates JR, Pirrit LA, Fleury P, Winship I, Beighton P, Connor JM. Sampson JR, et al. J Med Genet. 1989 Aug;26(8):511-6. doi: 10.1136/jmg.26.8.511. J Med Genet. 1989. PMID: 2769723 Free PMC article. - Application of intragenic DNA probes in prenatal screening for retinoblastoma gene carriers in the United Kingdom.
Onadim ZO, Mitchell CD, Rutland PC, Buckle BG, Jay M, Hungerford JL, Harper K, Cowell JK. Onadim ZO, et al. Arch Dis Child. 1990 Jul;65(7 Spec No):651-6. doi: 10.1136/adc.65.7_spec_no.651. Arch Dis Child. 1990. PMID: 1974756 Free PMC article. - Programs, databases, and expert systems for human geneticists--a survey.
Fischer C, Schweigert S, Spreckelsen C, Vogel F. Fischer C, et al. Hum Genet. 1996 Feb;97(2):129-37. doi: 10.1007/BF02265253. Hum Genet. 1996. PMID: 8566941 Review. - Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness.
Kenna P, Mansergh F, Millington-Ward S, Erven A, Kumar-Singh R, Brennan R, Farrar GJ, Humphries P. Kenna P, et al. Br J Ophthalmol. 1997 Mar;81(3):207-13. doi: 10.1136/bjo.81.3.207. Br J Ophthalmol. 1997. PMID: 9135384 Free PMC article. - Linkage of PGK1 to X-linked severe combined immunodeficiency (IMD4) allows predictive testing in families with no surviving male.
Goodship J, Levinsky R, Malcolm S. Goodship J, et al. Hum Genet. 1989 Dec;84(1):11-4. doi: 10.1007/BF00210662. Hum Genet. 1989. PMID: 2606471
MeSH terms
LinkOut - more resources
Full Text Sources