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Items: 1 to 20 of 180

1.

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.

PMID:
3014348
2.

Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene.

Monaco AP, Neve RL, Colletti-Feener C, Bertelson CJ, Kurnit DM, Kunkel LM.

Nature. 1986 Oct 16-22;323(6089):646-50.

PMID:
3773991
3.

Preferential deletion of exons in Duchenne and Becker muscular dystrophies.

Forrest SM, Cross GS, Speer A, Gardner-Medwin D, Burn J, Davies KE.

Nature. 1987 Oct 15-21;329(6140):638-40.

PMID:
2821406
5.

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.

PMID:
3614347
6.

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.

PMID:
2576185
7.

Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gels.

den Dunnen JT, Bakker E, Breteler EG, Pearson PL, van Ommen GJ.

Nature. 1987 Oct 15-21;329(6140):640-2.

PMID:
2889148
8.

Long-range restriction map around the Duchenne muscular dystrophy gene.

Burmeister M, Lehrach H.

Nature. 1986 Dec 11-17;324(6097):582-5.

PMID:
3024018
9.
10.

Molecular deletion patterns in Duchenne muscular dystrophy patients.

Lucotte G, David F, Levy C.

Ann Genet. 1989;32(4):214-9.

PMID:
2610487
11.

The use of field-inversion gel electrophoresis for deletion detection in Duchenne muscular dystrophy.

Chen JD, Denton MJ, Morgan G, Pearn JH, Mackinlay AG.

Am J Hum Genet. 1988 May;42(5):777-80.

12.

Gene deletions in X-linked muscular dystrophy.

Lindlöf M, Kiuru A, Kääriäinen H, Kalimo H, Lang H, Pihko H, Rapola J, Somer H, Somer M, Savontaus ML, et al.

Am J Hum Genet. 1989 Apr;44(4):496-503.

13.

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.

PMID:
2889144
14.

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.

15.

Screening of male patients with autosomal recessive Duchenne dystrophy through dystrophin and DNA studies.

Vainzof M, Pavanello RC, Pavanello-Filho I, Rapaport D, Passos-Bueno MR, Zubrzycka-Gaarn EE, Bulman DE, Zatz M.

Am J Med Genet. 1991 Apr 1;39(1):38-41.

PMID:
1867262
17.

Familial occurrence of Duchenne dystrophy through paternal lines in four families.

Zatz M, Passos-Bueno MR, Rapaport D, Vainzof M.

Am J Med Genet. 1991 Jan;38(1):80-4.

PMID:
1849353
18.

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.

PMID:
3040577
19.

Gene deletions in Japanese patients with Duchenne and Becker muscular dystrophy.

Asano J, Tomatsu S, Sukegawa K, Yamaguchi S, Ikedo Y, Minami R, Iida M, Nishimura M, Nakagawa M, Ohshiro M, et al.

Jinrui Idengaku Zasshi. 1990 Jun;35(2):159-68.

PMID:
2398631
20.

A molecular survey of Israeli Duchenne and Becker muscular dystrophy patients.

Legum C, Shomrat R, Glassner M, Shiloh Y.

Biomed Pharmacother. 1994;48(8-9):359-64.

PMID:
7858172

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