144 related articles for article (PubMed ID: 2887110)
1. Familial inheritance of a DXS164 deletion mutation from a heterozygous female.
Lanman JT; Pericak-Vance MA; Bartlett RJ; Chen JC; Yamaoka L; Koh J; Speer MC; Hung WY; Roses AD
Am J Hum Genet; 1987 Aug; 41(2):138-44. PubMed ID: 2887110
[TBL] [Abstract][Full Text] [Related]
2. Germline mosaicism and Duchenne muscular dystrophy mutations.
Bakker E; Van Broeckhoven C; Bonten EJ; van de Vooren MJ; Veenema H; Van Hul W; Van Ommen GJ; Vandenberghe A; Pearson PL
Nature; 1987 Oct 8-14; 329(6139):554-6. PubMed ID: 2889144
[TBL] [Abstract][Full Text] [Related]
3. Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy.
Monaco AP; Bertelson CJ; Colletti-Feener C; Kunkel LM
Hum Genet; 1987 Mar; 75(3):221-7. PubMed ID: 2881877
[TBL] [Abstract][Full Text] [Related]
4. A genetic linkage map of five marker loci in and around the Duchenne muscular dystrophy locus.
Chen JD; Hejtmancik JF; Romeo G; Lindlof M; Boehm C; Caskey CT; Kress W; Fischbeck KH; Dreier M; Serravalle S
Genomics; 1989 Jan; 4(1):105-9. PubMed ID: 2563349
[TBL] [Abstract][Full Text] [Related]
5. Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy.
Kunkel LM; Hejtmancik JF; Caskey CT; Speer A; Monaco AP; Middlesworth W; Colletti CA; Bertelson C; Müller U; Bresnan M; Shapiro F; Tantravahi U; Speer J; Latt SA; Bartlett R; Pericak-Vance MA; Roses AD; Thompson MW; Ray PN; Worton RG; Fischbeck KH; Gallano P; Coulon M; Duros C; Boue J; Junien C; Chelly J; Hamard G; Jeanpierre M; Lambert M; Kaplan JC; Emery A; Dorkins H; McGlade S; Davies KE; Boehm C; Arveiler B; Lemaire C; Morgan GJ; Denton MJ; Amos J; Bobrow M; Benham F; Boswinkel E; Cole C; Dubowitz V; Hart K; Hodgson S; Johnson L; Walker A; Roncuzzi L; Ferlini A; Nobile C; Romeo G; Wilcox DE; Affara NA; Ferguson-Smith MA; Lindolf M; Kaariainen H; de la Chapelle A; Ionasescu V; Searby C; Ionasescu R; Bakker E; van Ommen GJ; Pearson PL; Greenberg CR; Hamerton JL; Wrogemann K; Doherty RA; Polakowska R; Hyser C; Quirk S; Thomas N; Harper JF; Darras BT; Francke U
Nature; 1986 Jul 3-9; 322(6074):73-7. PubMed ID: 3014348
[TBL] [Abstract][Full Text] [Related]
6. Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome.
Davies KE; Smith TJ; Bundey S; Read AP; Flint T; Bell M; Speer A
J Med Genet; 1988 Jan; 25(1):9-13. PubMed ID: 3162536
[TBL] [Abstract][Full Text] [Related]
7. Linked polymorphic DNA markers in the prediction of X-linked muscular dystrophy.
Lindlöf M; Sistonen P; de la Chapelle A
Ann Hum Genet; 1987 Oct; 51(4):317-28. PubMed ID: 3482147
[TBL] [Abstract][Full Text] [Related]
8. Hot spot of recombination within DXS164 in the Duchenne muscular dystrophy gene.
Grimm T; Müller B; Dreier M; Kind E; Bettecken T; Meng G; Müller CR
Am J Hum Genet; 1989 Sep; 45(3):368-72. PubMed ID: 2570527
[TBL] [Abstract][Full Text] [Related]
9. Isolation of a random cosmid clone, cX5, which defines a new polymorphic locus DXS148 near the locus for Duchenne muscular dystrophy.
Hofker MH; Bergen AA; Skraastad MI; Bakker E; Francke U; Wieringa B; Bartley J; van Ommen GJ; Pearson PL
Hum Genet; 1986 Nov; 74(3):275-9. PubMed ID: 2877936
[TBL] [Abstract][Full Text] [Related]
10. DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21.
Greenberg CR; Hamerton JL; Nigli M; Wrogemann K
Am J Hum Genet; 1987 Aug; 41(2):128-37. PubMed ID: 3475976
[TBL] [Abstract][Full Text] [Related]
11. A small deletion in the Duchenne/Becker muscular dystrophy locus--a functionally important region?
Hart KA; Monaco AP; Kunkel LM; Bobrow M
Hum Genet; 1987 Sep; 77(1):88-91. PubMed ID: 3040577
[TBL] [Abstract][Full Text] [Related]
12. [Carrier detection and gene analysis in a Duchenne muscular dystrophy family].
Lu FM
Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1990 Aug; 23(4):231-3, 255. PubMed ID: 1979269
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.
Bakker E; Bonten EJ; De Lange LF; Veenema H; Majoor-Krakauer D; Hofker MH; Van Ommen GJ; Pearson PL
J Med Genet; 1986 Dec; 23(6):573-80. PubMed ID: 2879929
[TBL] [Abstract][Full Text] [Related]
15. Molecular-genetic study of Duchenne and Becker muscular dystrophies: deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females.
Sugino S; Fujishita S; Kamimura N; Matsumoto T; Wapenaar MC; Deng HX; Shibuya N; Miike T; Niikawa N
Am J Med Genet; 1989 Dec; 34(4):555-61. PubMed ID: 2576185
[TBL] [Abstract][Full Text] [Related]
16. Germinal mosaicism in Duchenne muscular dystrophy.
Wood S; McGillivray BC
Hum Genet; 1988 Mar; 78(3):282-4. PubMed ID: 3346017
[TBL] [Abstract][Full Text] [Related]
17. A cDNA clone from the Duchenne/Becker muscular dystrophy gene.
Burghes AH; Logan C; Hu X; Belfall B; Worton RG; Ray PN
Nature; 1987 Jul 30-Aug 5; 328(6129):434-7. PubMed ID: 3614347
[TBL] [Abstract][Full Text] [Related]
18. A grandpaternally derived de novo deletion within Xp21 initially presenting in carrier females diagnosed as Kugelberg-Welander syndrome.
Wood S; Shukin RJ; McGillivray BC; Ray PN; Worton RG
Am J Med Genet; 1988 Feb; 29(2):419-23. PubMed ID: 2895584
[TBL] [Abstract][Full Text] [Related]
19. DNA deletions in mild and severe Becker muscular dystrophy.
Hart KA; Hodgson S; Walker A; Cole CG; Johnson L; Dubowitz V; Bobrow M
Hum Genet; 1987 Mar; 75(3):281-5. PubMed ID: 3030926
[TBL] [Abstract][Full Text] [Related]
20. Duchenne muscular dystrophy due to familial Xp21 deletion detectable by DNA analysis and flow cytometry.
Wilcox DE; Cooke A; Colgan J; Boyd E; Aitken DA; Sinclair L; Glasgow L; Stephenson JB; Ferguson-Smith MA
Hum Genet; 1986 Jun; 73(2):175-80. PubMed ID: 3721503
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]