183 related articles for article (PubMed ID: 5149523)
1. Confirmation of linkage of the loci for myotonic dystrophy and ABH secretion.
Renwick JH; Bundey SE; Ferguson-Smith MA; Izatt MM
J Med Genet; 1971 Dec; 8(4):407-16. PubMed ID: 5149523
[No Abstract] [Full Text] [Related]
2. Genetic linkage confirmed between the locus for myotonic dystrophy and the ABH-secretion and Lutheran blood group loci.
Harper PS; Rivas ML; Bias WB; Hutchinson JR; Dyken PR; McKusick VA
Am J Hum Genet; 1972 May; 24(3):310-6. PubMed ID: 5063795
[No Abstract] [Full Text] [Related]
3. Prenatal prediction in myotonic dystrophy: guidelines for genetic counseling.
Schrott HG; Karp L; Omenn GS
Clin Genet; 1973; 4(1):38-45. PubMed ID: 4570861
[No Abstract] [Full Text] [Related]
4. Genetic linkage between the loci for myotonic dystrophy and peptidase D.
O'Brien T; Ball S; Sarfarazi M; Harper PS; Robson EB
Ann Hum Genet; 1983 May; 47(2):117-21. PubMed ID: 6881909
[TBL] [Abstract][Full Text] [Related]
5. Myotonic dystrophy: opportunities for prenatal prediction.
Schrott HG; Omenn GS
Neurology; 1975 Aug; 25(8):789-91. PubMed ID: 1171415
[TBL] [Abstract][Full Text] [Related]
6. Linkage analysis of peripheral neurofibromatosis (Von Recklinghausen disease) and chromosome 19 markers linked to myotonic dystrophy.
Huson SM; Meredith AL; Sarfarazi M; Shaw DJ; Compston DA; Harper PS
J Med Genet; 1986 Feb; 23(1):55-7. PubMed ID: 3081725
[TBL] [Abstract][Full Text] [Related]
7. Additions to the myotonic dystrophy linkage group.
Larsen B; Johnson G; Van Loghem E; Newton RM; Pryse-Phillips W
Clin Genet; 1979 Jun; 15(6):513-7. PubMed ID: 466851
[TBL] [Abstract][Full Text] [Related]
8. An analysis procedure illustrated on a triple linkage of use for prenatal diagnosis of myotonic dystrophy.
Renwick JH; Bolling DR
J Med Genet; 1971 Dec; 8(4):399-406. PubMed ID: 5149522
[No Abstract] [Full Text] [Related]
9. [Eugenic significance of linkage between the gene loci for dystrophia myotonica (Steiner's disease) and ABH-secretor].
Zimmerli O; Moser H; Lattke F; von Matt B; Gerber H
Schweiz Med Wochenschr; 1977 Mar; 107(10):327-35. PubMed ID: 847432
[TBL] [Abstract][Full Text] [Related]
10. Detection of heterozygotes for myotonic dystrophy.
Bundey S
Clin Genet; 1974; 5(2):107-9. PubMed ID: 4829421
[No Abstract] [Full Text] [Related]
11. Myotonic dystrophy: linkage with apolipoprotein E and estimation of the gene carrier status with genetic markers.
Thibault MC; Mathieu J; Moorjani S; Lescault A; Prévost C; Gaudet D; Morissette J; Laberge C
Can J Neurol Sci; 1989 Feb; 16(1):134-40. PubMed ID: 2924208
[TBL] [Abstract][Full Text] [Related]
12. Genetic counselling for myotonic dystrophy: a comparison of lens examination and DNA linkage studies.
Longstaff S; Curtis D; Quick J; Talbot J
Eye (Lond); 1991; 5 ( Pt 1)():93-8. PubMed ID: 1676377
[TBL] [Abstract][Full Text] [Related]
13. The use of linkage in genetic counselling.
Mayo O
Hum Hered; 1970; 20(5):473-85. PubMed ID: 5512122
[No Abstract] [Full Text] [Related]
14. Myotonic dystrophy: some genetic problems.
Harper PS
Birth Defects Orig Artic Ser; 1974; 10(10):120-5. PubMed ID: 4462623
[No Abstract] [Full Text] [Related]
15. [Screening for heterozygotes in a large family suffering from Steinert's disease with varying clinical manifestations (author's transl)].
Marcoz JP
J Genet Hum; 1978 Sep; 26(3):237-74. PubMed ID: 739261
[TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis for the unstable CTG repeat sequence in myotonic dystrophy: a retrospective study in a French family.
Lucotte G; Berriche S; David F; Mariotti M; Turpin JC
Genet Couns; 1994; 5(2):171-4. PubMed ID: 7917127
[TBL] [Abstract][Full Text] [Related]
17. Gene mapping and myotonic dystrophy.
Harper PS; Shaw D; Meredith L; Sarfarazi M; Brook D; Huson S
Prog Clin Biol Res; 1985; 177():61-76. PubMed ID: 2989839
[No Abstract] [Full Text] [Related]
18. Cataract and myotonic dystrophy: the role of molecular diagnosis.
Reardon W; MacMillan JC; Myring J; Harley HG; Rundle SA; Beck L; Harper PS; Shaw DJ
Br J Ophthalmol; 1993 Sep; 77(9):579-83. PubMed ID: 8218057
[TBL] [Abstract][Full Text] [Related]
19. 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
J Med Genet; 1983 Aug; 20(4):259-63. PubMed ID: 6620325
[TBL] [Abstract][Full Text] [Related]
20. [Direct genotype analysis in congenital myotonic dystrophy with an unusual family anamnesis].
Bindl L; Rummel W; Walter S; Haverkamp F; Kowalewski S; Lentze MJ; Koch M
Klin Padiatr; 1993; 205(5):367-9. PubMed ID: 8411905
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]