Multilocus linkage analysis in humans: detection of linkage and estimation of recombination.

Keywords

Linkage (software), Genetic linkage, Genetics, Biology, Recombination

References

• Easy calculations of lod scores and genetic risks on small computers.G.M. Lathrop, J.-M. Lalouel — 1984
• Construction of a genetic linkage map in man using restriction fragment length polymorphisms.David Botstein, R. White, Mark H. Skolnick — 1980
• Beta-globin locus is linked to the parathyroid hormone (PTH) locus and lies between the insulin and PTH loci in man.Stylianos E. Antonarakis, John A. Phillips, Richard L. Mallonee — 1983
• A general model for the genetic analysis of pedigree data.Robert C. Elston, Jason A. Stewart — 1971
• Strategies for multilocus linkage analysis in humans.G.M. Lathrop, J.-M. Lalouel, Cécile Julier — 1984
• Probability functions on complex pedigreesC. Cannings, E. A. Thompson, Mark H. Skolnick — 1978
• Extensions to pedigree analysis I. Likehood calculations for simple and complex pedigrees.Kenneth Lange, R.C. Elston — 1975
• A mapping function for man.D. C. Rao, N.E. Morton, J. Lindsten — 1977
• An alternative model of recombination and interferenceNeil Risch, Kenneth Lange — 1979
• Classifications and comparisons of multilocus recombination distributions.Samuel Karlin, Uri Liberman — 1978
• The use of computers.J.H. Edwards — 1982
• The theory of genetical recombination. I. Long-chromosome armsAndrew Owen — 1949
• A mathematically tractable family of genetic mapping functions with different amounts of interference.Joseph Felsenstein — 1979
• A mapping function for human chromosomesE. Sturt — 1976
• A natural class of multilocus recombination processes and related measures of crossover interferenceSamuel Karlin, Uri Liberman — 1979
• Statistical analysis of multilocus recombination.Neil Risch, Kenneth Lange — 1983

Cited by

• Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11.Ángel Rubio Castro — 1992
• Genetic and physical mapping of a novel region close to the fragile X site on the human X chromosome.照美 稲垣, 一美 宮内, 尚美 木村 — 1989
• Linkage analysis of French families with facioscapulohumeral muscular dystrophy.Carole C. Wedge, Thomas D. Kearns — 1989
• The human "interferon-beta 2/hepatocyte stimulating factor/interleukin-6" gene: DNA polymorphism studies and localization to chromosome 7p21.Carlos Martínez de Campos — 1988
• Benign familial neonatal convulsions linked to genetic markers on chromosome 20Heidi Haywood Dowell — 1989
• Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17.Malie Montagutelli — 1987
• Bayesian multilocus linkage mapping.Robert D. Blank, Gordon Campbell, Martin R. Pollak — 1988
• An autosomal genomic screen for autism.Collaborative Linkage Study of Autism — 1999
• Exclusion of linkage to 14q23‐24 in a family with Holt‐Oram syndromeMaría Alejandra López Ollero — 1994
• Carrier detection of Werner's syndrome using a microsatellite that exhibits linkage disequilibrium with the Werner's syndrome locusMariano Grajal Blanco — 1994
• Genetic linkage analysis of Canadian spinal muscular atrophy kindreds using flanking microsatellite 5q13 polymorphismsYa. I. Korenman, A. T. Alymova, E.I. Bobrinskaya — 2004
• Autosomal dominant polycystic kidney disease: localization of the second gene to chromosome 4q13-q23.Virginia Gibson, Rachael Luck — 1993
• Germ-line mosaicism simulates genetic heterogeneity in Wiskott-Aldrich syndrome.Benoı̂t Arveiler, Geneviève de Saint Basile, Alain Fischer — 1990
• Age-related cognitive decline in hereditary spastic paraparesis linked to chromosome 2pKeith Bernhard — 2000
• Mutations of the PKD1 gene among Japanese autosomal dominant polycystic kidney disease patients, including one heterozygous mutation identified in members of the same familyEdelby Escobar Carmona, Vicente Eloy Fardales Macías, Enrique Abraham Marcel — 2001
• Clinical and Genetic Analysis of a New Multigenerational Pedigree with GEFS+ (Generalized Epilepsy with Febrile Seizures Plus)裕之 岡部, 俊行 渡辺, 有二 竜 — 2002
• Spinal cord magnetic resonance imaging in autosomal dominant hereditary spastic paraplegiaOscar López de Guereño Urisabel — 2005
• A system for exact and approximate genetic linkage analysis of SNP data in large pedigrees幸裕 川浦 — 2013
• Genetic analysis of 24 French families with multiple endocrine neoplasia type 2A.S A Narod, M. F. Lavoué, Kevin Morgan — 1992
• Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1.Kevin M. Flanigan, Kathy Gardner, Kathy Alderson — 1996

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