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43. Failure to demonstrate linkage between the loci for the Rh and Duffy blood groups. Sanger R; Tippett P; Gavin J; Race RR Ann Hum Genet; 1973 Jan; 36(3):353-4. PubMed ID: 4714425 [No Abstract] [Full Text] [Related]
44. Minimal expression of myotonic dystrophy: a clinical and molecular analysis. Reardon W; Harley HG; Brook JD; Rundle SA; Crow S; Harper PS; Shaw DJ J Med Genet; 1992 Nov; 29(11):770-3. PubMed ID: 1453424 [TBL] [Abstract][Full Text] [Related]
45. Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspring. Redman JB; Fenwick RG; Fu YH; Pizzuti A; Caskey CT JAMA; 1993 Apr; 269(15):1960-5. PubMed ID: 8464127 [TBL] [Abstract][Full Text] [Related]
46. [Myotonia dystrophica]. Grinshteĭn AB; Goretov AP; Belyĭ EA Zh Nevrol Psikhiatr Im S S Korsakova; 1993; 93(5):17-9. PubMed ID: 8154209 [TBL] [Abstract][Full Text] [Related]
47. Characterization and polymerase chain reaction (PCR) detection of an Alu deletion polymorphism in total linkage disequilibrium with myotonic dystrophy. Mahadevan MS; Foitzik MA; Surh LC; Korneluk RG Genomics; 1993 Feb; 15(2):446-8. PubMed ID: 8449517 [TBL] [Abstract][Full Text] [Related]
48. Genetics and linkage relationships of the C3 polymorphism: discovery of C3-Se linkage and assignment of LES-C3-DM-Se-PEPD-Lu synteny to chromosome 19. Eiberg H; Mohr J; Nielsen LS; Simonsen N Clin Genet; 1983 Sep; 24(3):159-70. PubMed ID: 6627719 [TBL] [Abstract][Full Text] [Related]
55. [A case of myotonic dystrophy proved by DNA analysis]. Juryńczyk J; Weglewski A Neurol Neurochir Pol; 1998; 32(5):1267-71. PubMed ID: 10463239 [TBL] [Abstract][Full Text] [Related]
56. Introduction to blood group genetics. Polesky HF Mayo Clin Proc; 1977 Mar; 52(3):136-40. PubMed ID: 402510 [No Abstract] [Full Text] [Related]
57. Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophy. Meredith AL; Huson SM; Lunt PW; Sarfarazi M; Harley HG; Brook JD; Shaw DJ; Harper PS Br Med J (Clin Res Ed); 1986 Nov; 293(6558):1353-6. PubMed ID: 2878705 [TBL] [Abstract][Full Text] [Related]
58. Five years experience of predictive testing for myotonic dystrophy using linked DNA markers. Reardon W; Floyd JL; Myring J; Lazarou LP; Meredith AL; Harper PS Am J Med Genet; 1992 Aug; 43(6):1006-11. PubMed ID: 1415325 [TBL] [Abstract][Full Text] [Related]
59. Autosomal linkage in humans (methodology and results of computer analysis). Falk CT; Walker ME; Martin MD; Allen FH Ser Haematol; 1975; 8(2):153-237. PubMed ID: 1198129 [No Abstract] [Full Text] [Related]
60. Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies. Ott J Am J Hum Genet; 1974 Sep; 26(5):588-97. PubMed ID: 4422075 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]