135 related articles for article (PubMed ID: 3928103)
21. Molecular biological approaches to genetic disorders in prenatal diagnosis.
Katayama S
Early Hum Dev; 1992; 29(1-3):149-53. PubMed ID: 1356752
[TBL] [Abstract][Full Text] [Related]
22. Use of dystrophin genomic and cDNA probes for solving difficulties in carrier detection and prenatal diagnosis of Duchenne muscular dystrophy.
Shomrat R; Driks N; Legum C; Shiloh Y
Am J Med Genet; 1992 Feb; 42(3):281-7. PubMed ID: 1536162
[TBL] [Abstract][Full Text] [Related]
23. Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome.
Davies KE; Pearson PL; Harper PS; Murray JM; O'Brien T; Sarfarazi M; Williamson R
Nucleic Acids Res; 1983 Apr; 11(8):2303-12. PubMed ID: 6304647
[TBL] [Abstract][Full Text] [Related]
24. Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome.
Kingston HM; Thomas NS; Pearson PL; Sarfarazi M; Harper PS
J Med Genet; 1983 Aug; 20(4):255-8. PubMed ID: 6620324
[TBL] [Abstract][Full Text] [Related]
25. The use of linked DNA polymorphisms for genotype prediction in families with Duchenne muscular dystrophy.
Harper PS; O'Brien T; Murray JM; Davies KE; Pearson P; Williamson R
J Med Genet; 1983 Aug; 20(4):252-4. PubMed ID: 6684693
[TBL] [Abstract][Full Text] [Related]
26. Prenatal diagnosis of Duchenne muscular dystrophy by DNA analysis.
Old JM; Davies KE
J Med Genet; 1986 Dec; 23(6):556-9. PubMed ID: 2879927
[TBL] [Abstract][Full Text] [Related]
27. Prenatal diagnosis in a female carrying a deletion close to the Duchenne locus.
Børresen AL; Boman H; Møller P; Berg K
Prenat Diagn; 1988 Jan; 8(1):67-72. PubMed ID: 3422736
[TBL] [Abstract][Full Text] [Related]
28. [Echoscopic diagnosis of the heterozygote carrier state in Duchenne's muscular dystrophy].
Krasil'nikov VV; Lazebnik TA; Prokof'ev GV
Zh Nevropatol Psikhiatr Im S S Korsakova; 1988; 88(11):18-9. PubMed ID: 3066080
[TBL] [Abstract][Full Text] [Related]
29. Update on the molecular genetics of Duchenne muscular dystrophy.
Siddique T; Bartlett R; Pericak-Vance M; Yamaoka L; Koh J; Chen J; Hung WY; Kandt R; Roses AD
Aust Paediatr J; 1988; 24 Suppl 1():9-14. PubMed ID: 3060079
[TBL] [Abstract][Full Text] [Related]
30. [DNA diagnosis of Duchenne muscular dystrophy].
Matsumoto T
No To Shinkei; 1991 May; 43(5):421-8. PubMed ID: 1680358
[No Abstract] [Full Text] [Related]
31. [Prenatal diagnosis of Duchenne's muscular dystrophy fetus at risk].
Hua XY; Xu MH; Lin QD
Zhonghua Fu Chan Ke Za Zhi; 1994 Jul; 29(7):408-10, 445. PubMed ID: 8001417
[TBL] [Abstract][Full Text] [Related]
32. DNA analysis of Duchenne and Becker muscular dystrophy using pERT87 genomic probes and dystrophin cDNA probes--establishing the optimum strategy for carrier diagnosis in the Japanese population.
Ubagai T; Katayama S
Jinrui Idengaku Zasshi; 1991 Sep; 36(3):211-27. PubMed ID: 1684391
[TBL] [Abstract][Full Text] [Related]
33. Prenatal diagnosis of Duchenne muscular dystrophy by restriction fragment length polymorphism analysis with pERT 87 intragenomic deoxyribonucleic acid probes.
Katayama S; Yano T; Takeshita N; Abe Y; Usui A; Kubo H; Momose K; Ubagai T
Nihon Sanka Fujinka Gakkai Zasshi; 1991 Jun; 43(6):633-40. PubMed ID: 1677375
[TBL] [Abstract][Full Text] [Related]
34. Genetic linkage relationship between the Xg blood group system and two X chromosome DNA polymorphisms in families with Duchenne and Becker muscular dystrophy.
Sarfarazi M; Harper PS; Kingston HM; Murray JM; O'Brien T; Davies KE; Williamson R; Tippett P; Sanger R
Hum Genet; 1983; 65(2):169-71. PubMed ID: 6317539
[TBL] [Abstract][Full Text] [Related]
35. Somatic mosaicism at the Duchenne locus.
Lebo RV; Olney RK; Golbus MS
Am J Med Genet; 1990 Oct; 37(2):187-90. PubMed ID: 1978985
[TBL] [Abstract][Full Text] [Related]
36. Linkage studies in Duchenne and Becker muscular dystrophies.
Walker A; Hart K; Cole C; Hodgson S; Johnson L; Dubowitz V; Bobrow M
J Med Genet; 1986 Dec; 23(6):538-47. PubMed ID: 2879925
[TBL] [Abstract][Full Text] [Related]
37. [Discriminant analysis of methods for detecting the heterozygote carrier state for the Duchenne muscular dystrophy gene].
Khrennikov VIu; Sitnikov VF; Deev AI; Svintsitskiĭ IV
Zh Nevropatol Psikhiatr Im S S Korsakova; 1988; 88(11):14-8. PubMed ID: 3223151
[TBL] [Abstract][Full Text] [Related]
38. [Use of dystrophin c-DNA for the direct diagnosis of Duchenne muscular dystrophy in female carriers].
Baiget M; del Río E; Gallano P
Neurologia; 1989 Oct; 4(8):268-76. PubMed ID: 2576910
[TBL] [Abstract][Full Text] [Related]
39. [Clinical polymorphism and genetic heterogeneity in Duchenne's progressive muscular dystrophy in girls (a review)].
Zavadenko NN; Temin PA; Malygina NA
Zh Nevropatol Psikhiatr Im S S Korsakova; 1988; 88(11):123-6. PubMed ID: 3066079
[No Abstract] [Full Text] [Related]
40. [Carrier diagnosis and prenatal prognosis using DNA analysis in X-chromosome-linked Duchenne and Becker muscular dystrophy].
Moser H; Liechti-Gallati S; Braga S; Hirsiger H
Schweiz Med Wochenschr; 1987 Dec; 117(51):2061-73. PubMed ID: 3433090
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]