Genetic linkage confirmed between the locus for myotonic dystrophy and the ABH-secretion and Lutheran blood group loci - PubMed (original) (raw)

• PMID: 5063795
• PMCID: PMC1762284

Genetic linkage confirmed between the locus for myotonic dystrophy and the ABH-secretion and Lutheran blood group loci

P S Harper et al. Am J Hum Genet. 1972 May.

No abstract available

PubMed Disclaimer

Similar articles

• An analysis procedure illustrated on a triple linkage of use for prenatal diagnosis of myotonic dystrophy.
  Renwick JH, Bolling DR. Renwick JH, et al. J Med Genet. 1971 Dec;8(4):399-406. doi: 10.1136/jmg.8.4.399. J Med Genet. 1971. PMID: 5149522 Free PMC article. No abstract available.
• Confirmation of linkage of the loci for myotonic dystrophy and ABH secretion.
  Renwick JH, Bundey SE, Ferguson-Smith MA, Izatt MM. Renwick JH, et al. J Med Genet. 1971 Dec;8(4):407-16. doi: 10.1136/jmg.8.4.407. J Med Genet. 1971. PMID: 5149523 Free PMC article. No abstract available.
• Amniotic fluid secretor typing: validation for use in prenatal prediction of myotonic dystrophy.
  Teichler-Zallen D, Doherty RA. Teichler-Zallen D, et al. Clin Genet. 1980 Oct;18(4):257-67. doi: 10.1111/j.1399-0004.1980.tb00883.x. Clin Genet. 1980. PMID: 6449321
• Myotonic dystrophy and gene mapping on human chromosome 19.
  Brook JD, Shaw DJ, Meredith AL. Brook JD, et al. Biotechnol Genet Eng Rev. 1985;3:311-47. doi: 10.1080/02648725.1985.10647817. Biotechnol Genet Eng Rev. 1985. PMID: 3004536 Review. No abstract available.
• [Myotonic dystrophy of Steinert].
  Junien C. Junien C. J Genet Hum. 1989 Jan;37(1):51-4. J Genet Hum. 1989. PMID: 2565953 Review. French.

Cited by

• Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe.
  Davies KE, Jackson J, Williamson R, Harper PS, Ball S, Sarfarazi M, Meredith L, Fey G. Davies KE, et al. J Med Genet. 1983 Aug;20(4):259-63. doi: 10.1136/jmg.20.4.259. J Med Genet. 1983. PMID: 6620325 Free PMC article.
• Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19q.
  Harley HG, Walsh KV, Rundle S, Brook JD, Sarfarazi M, Koch MC, Floyd JL, Harper PS, Shaw DJ. Harley HG, et al. Hum Genet. 1991 May;87(1):73-80. doi: 10.1007/BF01213096. Hum Genet. 1991. PMID: 2037285
• Presymptomatic detection and prenatal diagnosis for myotonic dystrophy by means of linked DNA markers.
  Norman AM, Floyd JL, Meredith AL, Harper PS. Norman AM, et al. J Med Genet. 1989 Dec;26(12):750-4. doi: 10.1136/jmg.26.12.750. J Med Genet. 1989. PMID: 2575669 Free PMC article.
• Evidence for linkage of Charcot-Marie-Tooth neuropathy to the Duffy locus on chromosome 1.
  Bird TD, Ott J, Giblett ER. Bird TD, et al. Am J Hum Genet. 1982 May;34(3):388-94. Am J Hum Genet. 1982. PMID: 6952764 Free PMC article.
• The prenatal diagnosis of metabolic disorders.
  Harper PS. Harper PS. J R Coll Physicians Lond. 1973 Apr;7(3):251-8. J R Coll Physicians Lond. 1973. PMID: 4633369 Free PMC article. Review. No abstract available.

References

1. 1. Am J Med Sci. 1968 Jun;255:368-75 - PubMed
2. 1. Br Med Bull. 1969 Jan;25(1):65-73 - PubMed
3. 1. Lancet. 1969 Aug 16;2(7616):386 - PubMed
4. 1. J Med Genet. 1971 Dec;8(4):399-406 - PubMed
5. 1. J Med Genet. 1971 Dec;8(4):407-16 - PubMed

MeSH terms

Substances

LinkOut - more resources

• Full Text Sources

  • Europe PubMed Central
  • PubMed Central