116 related articles for article (PubMed ID: 2570401)
1. Detection of novel genetic markers by mismatch analysis.
Roberts RG; Montandon AJ; Bobrow M; Bentley DR
Nucleic Acids Res; 1989 Aug; 17(15):5961-71. PubMed ID: 2570401
[TBL] [Abstract][Full Text] [Related]
2. An informative polymorphism detectable by polymerase chain reaction at the 3' end of the dystrophin gene.
Oudet C; Heilig R; Mandel JL
Hum Genet; 1990 Feb; 84(3):283-5. PubMed ID: 1968037
[TBL] [Abstract][Full Text] [Related]
3. [Molecular genetics of Duchenne's disease].
Bolhuis PA
Ned Tijdschr Geneeskd; 1989 Jul; 133(27):1347-8. PubMed ID: 2571948
[No Abstract] [Full Text] [Related]
4. Dystrophin-related muscular dystrophies.
Witkowski JA
J Child Neurol; 1989 Oct; 4(4):251-71. PubMed ID: 2571631
[TBL] [Abstract][Full Text] [Related]
5. Normal human genomic restriction-fragment patterns and polymorphisms revealed by hybridization with the entire dystrophin cDNA.
Darras BT; Francke U
Am J Hum Genet; 1988 Nov; 43(5):612-9. PubMed ID: 2903662
[TBL] [Abstract][Full Text] [Related]
6. Gene mapping and the muscular dystrophies.
Harper PS
Prog Clin Biol Res; 1989; 306():29-49. PubMed ID: 2567999
[No Abstract] [Full Text] [Related]
7. [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]
8. High resolution deletion breakpoint mapping in the DMD gene by whole cosmid hybridization.
Blonden LA; den Dunnen JT; van Paassen HM; Wapenaar MC; Grootscholten PM; Ginjaar HB; Bakker E; Pearson PL; van Ommen GJ
Nucleic Acids Res; 1989 Jul; 17(14):5611-21. PubMed ID: 2569720
[TBL] [Abstract][Full Text] [Related]
9. A new polymorphism for the dystrophin intragenic probe P20 [DXS269] using BstX1.
Robertson ME; Wapenaar MC; Malcolm S
Nucleic Acids Res; 1989 Apr; 17(8):3327. PubMed ID: 2566969
[No Abstract] [Full Text] [Related]
10. Direct method for prenatal diagnosis and carrier detection in Duchenne/Becker muscular dystrophy using the entire dystrophin cDNA.
Darras BT; Koenig M; Kunkel LM; Francke U
Am J Med Genet; 1988 Mar; 29(3):713-26. PubMed ID: 2897793
[TBL] [Abstract][Full Text] [Related]
11. Rapid detection of CA polymorphisms in cloned DNA: application to the 5' region of the dystrophin gene.
Feener CA; Boyce FM; Kunkel LM
Am J Hum Genet; 1991 Mar; 48(3):621-7. PubMed ID: 1998344
[TBL] [Abstract][Full Text] [Related]
12. DNA restriction fragment length polymorphisms in differential diagnosis of genetic disease: application in neuromuscular diseases.
Defesche JC; de Vissar M; Bakker E; Bouwsma G; de Vijlder JJ; Bolhuis PA
Hum Genet; 1989 Apr; 82(1):55-8. PubMed ID: 2565867
[TBL] [Abstract][Full Text] [Related]
13. A BanI RFLP at a deletion hotspot in the human dystrophin gene.
Read AP; Mountford R
Nucleic Acids Res; 1990 Jan; 18(2):385. PubMed ID: 1970164
[No Abstract] [Full Text] [Related]
14. Heteroduplex analysis of the dystrophin gene: application to point mutation and carrier detection.
Prior TW; Papp AC; Snyder PJ; Sedra MS; Western LM; Bartolo C; Moxley RT; Mendell JR
Am J Med Genet; 1994 Mar; 50(1):68-73. PubMed ID: 8160755
[TBL] [Abstract][Full Text] [Related]
15. Rapid DNA haplotyping using a multiplex heteroduplex approach: application to Duchenne muscular dystrophy carrier testing.
Prior TW; Wenger GD; Papp AC; Snyder PJ; Sedra MS; Bartolo C; Moore JW; Highsmith WE
Hum Mutat; 1995; 5(3):263-8. PubMed ID: 7599638
[TBL] [Abstract][Full Text] [Related]
16. Usefulness of dinucleotide polymorphism markers in genetic analysis of Duchenne's muscular dystrophy cases in Singapore.
Lai PS; Chiu LL; Low PS; Lee WL; Tay JS
Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():175-8. PubMed ID: 8629101
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. A new approach to gene diagnosis of Duchenne/Becker muscular dystrophy--amplified fragment length polymorphisms.
Xu S; Huang S; Lo WH
Chin Med Sci J; 1994 Sep; 9(3):137-42. PubMed ID: 7865831
[TBL] [Abstract][Full Text] [Related]
19. RFLP for Duchenne muscular dystrophy cDNA clone 44-1.
Laing NG; Siddique T; Bartlett RJ; Yamaoka LH; Chen JC; Walker AP; Hung WY; Roses AD
Nucleic Acids Res; 1988 Jul; 16(14B):7209. PubMed ID: 2900496
[No Abstract] [Full Text] [Related]
20. MspI RFLP for Duchenne muscular dystrophy cDNA subclone 9.
Wagner M; Reiss J; Hentemann M; Thies U
Nucleic Acids Res; 1989 Apr; 17(8):3328. PubMed ID: 2471152
[No Abstract] [Full Text] [Related]
[Next] [New Search]
