225 related articles for article (PubMed ID: 9004137)
1. Identification of carriers of Duchenne/Becker muscular dystrophy by a novel method based on detection of junction fragments in the dystrophin gene.
Yamagishi H; Kato S; Hiraishi Y; Ishihara T; Hata J; Matsuo N; Takano T
J Med Genet; 1996 Dec; 33(12):1027-31. PubMed ID: 9004137
[TBL] [Abstract][Full Text] [Related]
2. Gene deletions in Japanese patients with Duchenne and Becker muscular dystrophies: deletion study and carrier detection.
Asano J; Tomatsu S; Sukegawa K; Ikedo Y; Minami R; Iida M; Nishimura M; Nakagawa M; Ohshiro M; Orii T
Clin Genet; 1991 Jun; 39(6):419-24. PubMed ID: 1863988
[TBL] [Abstract][Full Text] [Related]
3. Direct carrier detection by in situ suppression hybridization with cosmid clones of the Duchenne/Becker muscular dystrophy locus.
Ried T; Mahler V; Vogt P; Blonden L; van Ommen GJ; Cremer T; Cremer M
Hum Genet; 1990 Oct; 85(6):581-6. PubMed ID: 2227948
[TBL] [Abstract][Full Text] [Related]
4. Detection of dystrophin deletion carriers using FISH analysis.
Calvano S; Memeo E; Piemontese MR; Melchionda S; Bisceglia L; Gasparini P; Zelante L
Clin Genet; 1997 Jul; 52(1):17-22. PubMed ID: 9272708
[TBL] [Abstract][Full Text] [Related]
5. Detection of Duchenne and Becker muscular dystrophy carriers by quantitative multiplex polymerase chain reaction analysis.
Ioannou P; Christopoulos G; Panayides K; Kleanthous M; Middleton L
Neurology; 1992 Sep; 42(9):1783-90. PubMed ID: 1513470
[TBL] [Abstract][Full Text] [Related]
6. Molecular deletion patterns in families from southern France with Duchenne/Becker muscular dystrophies.
Claustres M; Tuffery S; Chevron MP; Jozelon MP; Martinez P; Echenne B; Demaille J
Hum Genet; 1991 Dec; 88(2):179-84. PubMed ID: 1684565
[TBL] [Abstract][Full Text] [Related]
7. Duplication detection in Japanese Duchenne muscular dystrophy patients and identification of carriers with partial gene deletions using pulsed-field gel electrophoresis.
Kodaira M; Hiyama K; Karakawa T; Kameo H; Satoh C
Hum Genet; 1993 Oct; 92(3):237-43. PubMed ID: 8406431
[TBL] [Abstract][Full Text] [Related]
8. Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutations.
Darras BT; Blattner P; Harper JF; Spiro AJ; Alter S; Francke U
Am J Hum Genet; 1988 Nov; 43(5):620-9. PubMed ID: 2903663
[TBL] [Abstract][Full Text] [Related]
9. Detection of carriers of deletions in the dystrophin gene in Bulgarian DMD-BMD families.
Bronzova J; Todorova A; Kalaydjieva L
Hum Genet; 1994 Feb; 93(2):170-4. PubMed ID: 8112741
[TBL] [Abstract][Full Text] [Related]
10. Deletions in the dystrophin gene: analysis of Duchenne and Becker muscular dystrophy patients in Quebec.
Simard LR; Gingras F; Delvoye N; Vanasse M; Melançon SB; Labuda D
Hum Genet; 1992 Jun; 89(4):419-24. PubMed ID: 1618490
[TBL] [Abstract][Full Text] [Related]
11. Determination of Duchenne muscular dystrophy carrier status by single strand conformation polymorphism analysis of deleted regions of the dystrophin locus.
Richards RI; Friend K
J Med Genet; 1991 Dec; 28(12):856-9. PubMed ID: 1757962
[TBL] [Abstract][Full Text] [Related]
12. [Difference of new mutation rates in dystrophin gene between deletion and duplication mutation in Duchenne and Becker muscular dystrophy].
Kawamura J; Kato S; Ishihara T; Hiraishi Y; Kawashiro T
Rinsho Shinkeigaku; 1997 Mar; 37(3):212-7. PubMed ID: 9217419
[TBL] [Abstract][Full Text] [Related]
13. [Carrier detection in families affected by Duchenne/Becker muscular dystrophy].
Pikó H; Nagy B; Balog J; Bán Z; Herczegfalvi A; Karcagi V
Orv Hetil; 2007 Dec; 148(51):2403-9. PubMed ID: 18055393
[TBL] [Abstract][Full Text] [Related]
14. Alternative splicing of dystrophin mRNA complicates carrier determination: report of a DMD family.
Lenk U; Demuth S; Kräft U; Hanke R; Speer A
J Med Genet; 1993 Mar; 30(3):206-9. PubMed ID: 8474106
[TBL] [Abstract][Full Text] [Related]
15. Southern blot and PCR analyses of dystrophin gene deletions in Japanese patients with Duchenne muscular dystrophy.
Nakajima T; Matsuo M; Nakamura H; Fujiwara Y
Kobe J Med Sci; 1991 Feb; 37(1):21-33. PubMed ID: 1921260
[TBL] [Abstract][Full Text] [Related]
16. Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients.
Shomrat R; Gluck E; Legum C; Shiloh Y
Am J Med Genet; 1994 Feb; 49(4):369-73. PubMed ID: 8160727
[TBL] [Abstract][Full Text] [Related]
17. [Detection of mutation in dystrophin gene in Duchenne muscular dystrophy--multiplex PCR and Southern blot analysis].
Kawamura J
Nihon Rinsho; 1997 Dec; 55(12):3126-30. PubMed ID: 9436422
[TBL] [Abstract][Full Text] [Related]
18. The clinical and molecular genetic approach to Duchenne and Becker muscular dystrophy: an updated protocol.
van Essen AJ; Kneppers AL; van der Hout AH; Scheffer H; Ginjaar IB; ten Kate LP; van Ommen GJ; Buys CH; Bakker E
J Med Genet; 1997 Oct; 34(10):805-12. PubMed ID: 9350811
[TBL] [Abstract][Full Text] [Related]
19. DNA polymorphisms and deletion analysis of the Duchenne-Becker muscular dystrophy gene in the Chinese.
Soong BW; Tsai TF; Su CH; Kao KP; Hsiao KJ; Su TS
Am J Med Genet; 1991 Mar; 38(4):593-600. PubMed ID: 1676564
[TBL] [Abstract][Full Text] [Related]
20. Topographic pattern of the rearrangement of the dystrophin gene in Japanese Duchenne muscular dystrophy.
Imoto N; Arinami T; Hamano K; Matsumura K; Yamada H; Hamaguchi H; Takita H
Hum Genet; 1993 Dec; 92(6):533-6. PubMed ID: 8262511
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
