Easy calculations of lod scores and genetic risks on small computers
- PMID: 6585139
- PMCID: PMC1684427
Easy calculations of lod scores and genetic risks on small computers
Abstract
A computer program that calculates lod scores and genetic risks for a wide variety of both qualitative and quantitative genetic traits is discussed. An illustration is given of the joint use of a genetic marker, affection status, and quantitative information in counseling situations regarding Duchenne muscular dystrophy.
Similar articles
-
Duchenne muscular dystrophy and idiopathic hyperCKemia in a family causing confusion in genetic counselling.Am J Med Genet. 1996 Dec 11;66(2):237-8. doi: 10.1002/(SICI)1096-8628(19961211)66:2<237::AID-AJMG22>3.0.CO;2-T. Am J Med Genet. 1996. PMID: 8958338 No abstract available.
-
Complex segregation analysis and computer-assisted genetic risk assessment for Duchenne muscular dystrophy.Am J Med Genet. 1983 Feb;14(2):315-33. doi: 10.1002/ajmg.1320140212. Am J Med Genet. 1983. PMID: 6837627
-
DUCHEN: an interactive computer program for calculating heterozygosity (carrier) risks in X-linked recessive lethal diseases, and its application in Duchenne muscular dystrophy.Am J Med Genet. 1986 Oct;25(2):211-8. doi: 10.1002/ajmg.1320250203. Am J Med Genet. 1986. PMID: 3777018
-
[Genetics of muscular dystrophies].Recenti Prog Med. 1977 May;62(5):489-511. Recenti Prog Med. 1977. PMID: 329369 Review. Italian. No abstract available.
-
Carrier detection and genetic counselling in Duchenne dystrophy.Dev Med Child Neurol. 1975 Jun;17(3):352-6. doi: 10.1111/j.1469-8749.1975.tb04674.x. Dev Med Child Neurol. 1975. PMID: 1107098 Review. No abstract available.
Cited by
-
Linkage of cystic fibrosis to two tightly linked DNA markers: joint report from a collaborative study.Am J Hum Genet. 1986 Dec;39(6):681-93. Am J Hum Genet. 1986. PMID: 3026171 Free PMC article.
-
A likelihood-based framework for variant calling and de novo mutation detection in families.PLoS Genet. 2012;8(10):e1002944. doi: 10.1371/journal.pgen.1002944. Epub 2012 Oct 4. PLoS Genet. 2012. PMID: 23055937 Free PMC article.
-
Lack of phenotypic effect of triallelic variation in SPATA7 in a family with Leber congenital amaurosis resulting from CRB1 mutations.Mol Vis. 2011;17:3326-32. Epub 2011 Dec 16. Mol Vis. 2011. PMID: 22219627 Free PMC article.
-
First trimester prenatal diagnosis and detection of carriers of haemophilia A using the linked DNA probe DX13.Br Med J (Clin Res Ed). 1985 Sep 21;291(6498):765-9. doi: 10.1136/bmj.291.6498.765. Br Med J (Clin Res Ed). 1985. PMID: 3929933 Free PMC article.
-
Close linkage of the Wilson's disease locus to D13S12 in the chromosomal region 13q21 and not to ESD in 13q14.Hum Genet. 1990 Oct;85(5):560-2. doi: 10.1007/BF00194238. Hum Genet. 1990. PMID: 2227943
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical