152 related articles for article (PubMed ID: 2471152)
1. 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]
2. 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]
3. An MspI polymorphism for the dystrophin intragenic probe J-47.
Meng G; Müller CR
Nucleic Acids Res; 1989 Aug; 17(16):6756. PubMed ID: 2476720
[No Abstract] [Full Text] [Related]
4. 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]
5. 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]
6. Significantly higher frequency of the MspI 2.2 kb allele of the Duchenne muscular dystrophy intragenic probe P-20 in the Chinese population.
Wei J; Guo Y; Chen B; Yang Y
Hum Genet; 1992; 90(1-2):149-50. PubMed ID: 1385293
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. MspI RFLP at 19q12-q13.1 identified by the anonymous DNA sequence p30B18 [D19S31].
Smeets H; Coerwinkel M; Schepens J; Brunner H; Schonk D; Ropers HH; Wieringa B
Nucleic Acids Res; 1989 May; 17(9):3627. PubMed ID: 2471158
[No Abstract] [Full Text] [Related]
9. RFLP for Duchenne muscular dystrophy cDNA clone 30-2.
Walker AP; Bartlett RJ; Laing NG; Siddique T; Yamaoka LH; Chen JC; Hung WY; Roses AD
Nucleic Acids Res; 1988 Sep; 16(18):9072. PubMed ID: 2902573
[No Abstract] [Full Text] [Related]
10. A rare MspI RFLP of the DMD probe p20 (DXS269).
Uhlhaas S; Bakker E; van Broeckhoven C; Barth-Schulz A; Friedl W
Hum Genet; 1992 Apr; 89(1):122. PubMed ID: 1374360
[No Abstract] [Full Text] [Related]
11. [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]
12. Dystrophin-related muscular dystrophies.
Witkowski JA
J Child Neurol; 1989 Oct; 4(4):251-71. PubMed ID: 2571631
[TBL] [Abstract][Full Text] [Related]
13. Gene mapping and the muscular dystrophies.
Harper PS
Prog Clin Biol Res; 1989; 306():29-49. PubMed ID: 2567999
[No Abstract] [Full Text] [Related]
14. PvuII RFLPs in the DMD gene detected by a subclone (cDMD1a) of the cDNA.
Deng HX; Niikawa N
Nucleic Acids Res; 1990 May; 18(10):3107. PubMed ID: 1971933
[No Abstract] [Full Text] [Related]
15. Duchenne muscular dystrophy (DMD) gene cDNA 8 PstI and TaqI polymorphisms involve exon 51 of the HindIII map.
Laing NG; Akkari PA; Chandler DC; Thomas HE; Layton MG; Mears ME; Kakulas BA
Nucleic Acids Res; 1990 Jul; 18(14):4284. PubMed ID: 1974044
[No Abstract] [Full Text] [Related]
16. 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]
17. Brother/sister pairs affected with early-onset, progressive muscular dystrophy: molecular studies reveal etiologic heterogeneity.
Francke U; Darras BT; Hersh JH; Berg BO; Miller RG
Am J Hum Genet; 1989 Jul; 45(1):63-72. PubMed ID: 2568091
[TBL] [Abstract][Full Text] [Related]
18. Duchenne muscular dystrophy: the gene and the protein.
Love DR; Davies KE
Mol Biol Med; 1989 Feb; 6(1):7-17. PubMed ID: 2666821
[No Abstract] [Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
