Ludwig J, Mrazek J
BMC Bioinformatics. 2024; 25(1):163.
PMID: 38664637
PMC: 11044567.
DOI: 10.1186/s12859-024-05786-7.
Wang L, Xu X
BMC Genet. 2006; 6 Suppl 1:S58.
PMID: 16451670
PMC: 1866725.
DOI: 10.1186/1471-2156-6-S1-S58.
Edwards A
Hum Genet. 2005; 118(3-4):515-30.
PMID: 16283389
DOI: 10.1007/s00439-005-0049-1.
Morton N
Am J Hum Genet. 1998; 62(3):690-7.
PMID: 9497238
PMC: 1376937.
DOI: 10.1086/301741.
Collins A, FREZAL J, Teague J, Morton N
Proc Natl Acad Sci U S A. 1996; 93(25):14771-5.
PMID: 8962130
PMC: 26211.
DOI: 10.1073/pnas.93.25.14771.
A general statistical model for detecting complex-trait loci by using affected relative pairs in a genome search.
Smalley S, Woodward J, Palmer C
Am J Hum Genet. 1996; 58(4):844-60.
PMID: 8644749
PMC: 1914671.
Pure hereditary spastic paraparesis: an exclusion map covering more than 40% of the autosomal genome.
van Deutekom J, Bruyn R, van den Boorn N, Sandkuijl L, Padberg G, Frants R
Hum Genet. 1994; 93(4):408-14.
PMID: 8168811
DOI: 10.1007/BF00201665.
Multipoint linkage map of the human pseudoautosomal region, based on single-sperm typing: do double crossovers occur during male meiosis?.
Schmitt K, Lazzeroni L, Foote S, Vollrath D, Fisher E, Goradia T
Am J Hum Genet. 1994; 55(3):423-30.
PMID: 8079986
PMC: 1918414.
Absence of linkage between the serum cholinesterase (CHE1) and rhesus (RH) loci.
Chautard-Freire-Maia E
Hum Genet. 1982; 60(3):284-6.
PMID: 6809594
DOI: 10.1007/BF00303021.
Interpretation of RFLP linkage data.
Clayton J
J Med Genet. 1984; 21(2):157-8.
PMID: 6716420
PMC: 1049251.
DOI: 10.1136/jmg.21.2.157.
Beta-globin locus is linked to the parathyroid hormone (PTH) locus and lies between the insulin and PTH loci in man.
Antonarakis S, Phillips 3rd J, Mallonee R, Kazazian Jr H, Fearon E, Waber P
Proc Natl Acad Sci U S A. 1983; 80(21):6615-9.
PMID: 6314332
PMC: 391220.
DOI: 10.1073/pnas.80.21.6615.
Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome.
Davies K, Pearson P, Harper P, Murray J, OBrien T, Sarfarazi M
Nucleic Acids Res. 1983; 11(8):2303-12.
PMID: 6304647
PMC: 325885.
DOI: 10.1093/nar/11.8.2303.
The Mendelian inheritance of a human X chromosome-specific DNA sequence polymorphism and its use in linkage studies of genetic disease.
Hill M, Davies K, Harper P, Williamson R
Hum Genet. 1982; 60(3):222-6.
PMID: 6286461
DOI: 10.1007/BF00303007.
Construction of a genetic linkage map in man using restriction fragment length polymorphisms.
Botstein D, White R, Skolnick M, Davis R
Am J Hum Genet. 1980; 32(3):314-31.
PMID: 6247908
PMC: 1686077.
Eyes on chromosomes.
Renwick J
J Med Genet. 1970; 7(3):239-43.
PMID: 5489092
PMC: 1468891.
DOI: 10.1136/jmg.7.3.239.
Genetic linkage analysis of human hemoglobin variants.
Nance W, Conneally M, Kang K, Reed T, Schroder J, Rose S
Am J Hum Genet. 1970; 22(4):453-9.
PMID: 5432289
PMC: 1706597.
A kindred of koilonychia: linkage data.
Schleutermann D, Bias W, MCKUSICK V
Am J Hum Genet. 1970; 22(4):390-5.
PMID: 5432288
PMC: 1706585.
ABH secretor status of the fetus: a genetic marker identifiable by amniocentesis.
Harper P, Bias W, Hutchinson J, MCKUSICK V
J Med Genet. 1971; 8(4):438-40.
PMID: 5149527
PMC: 1469112.
DOI: 10.1136/jmg.8.4.438.
Possible linkage between uncoiler chromosome Un 1 and amylase polymorphism Amy 2 loci.
KAMARYT J, Adamek R, Vrba M
Humangenetik. 1971; 11(3):213-20.
PMID: 5101659
DOI: 10.1007/BF00274740.
Genetic linkage confirmed between the locus for myotonic dystrophy and the ABH-secretion and Lutheran blood group loci.
Harper P, Rivas M, Bias W, Hutchinson J, DYKEN P, MCKUSICK V
Am J Hum Genet. 1972; 24(3):310-6.
PMID: 5063795
PMC: 1762284.