Similar articles for PMID: 1483053

Year	Number of Results
1987	1
1988	2
1989	9
1990	6
1991	11
1992	13
1993	15
1994	6
1995	5
1996	3
1997	7
1998	3
1999	5
2001	2
2002	1
2003	2
2004	2
2006	1
2007	2
2008	1
2009	1
2010	2
2011	2
2013	1
2014	2
2017	1
2018	1
2019	1
2024	0

1

Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy, with special reference to mental ability.

Hodgson SV, Abbs S, Clark S, Manzur A, Heckmatt JZ, Dubowitz V, Bobrow M. Hodgson SV, et al. Neuromuscul Disord. 1992;2(4):269-76. doi: 10.1016/0960-8966(92)90059-f. Neuromuscul Disord. 1992. PMID: 1483053

2

Detection of gene deletions in Chinese patients with Duchenne/Becker muscular dystrophy using CDNA probes and the polymerase chain reaction method.

Yuge L, Hui L, Bingdi X. Yuge L, et al. Life Sci. 1999;65(9):863-9. doi: 10.1016/s0024-3205(99)00316-1. Life Sci. 1999. PMID: 10465346

3

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. Claustres M, et al. Hum Genet. 1991 Dec;88(2):179-84. doi: 10.1007/BF00206068. Hum Genet. 1991. PMID: 1684565

4

Characterization of translational frame exception patients in Duchenne/Becker muscular dystrophy.

Winnard AV, Klein CJ, Coovert DD, Prior T, Papp A, Snyder P, Bulman DE, Ray PN, McAndrew P, King W, et al. Winnard AV, et al. Hum Mol Genet. 1993 Jun;2(6):737-44. doi: 10.1093/hmg/2.6.737. Hum Mol Genet. 1993. PMID: 8353493

5

Deletion status and intellectual impairment in Duchenne muscular dystrophy.

Bushby KM, Appleton R, Anderson LV, Welch JL, Kelly P, Gardner-Medwin D. Bushby KM, et al. Dev Med Child Neurol. 1995 Mar;37(3):260-9. doi: 10.1111/j.1469-8749.1995.tb12000.x. Dev Med Child Neurol. 1995. PMID: 7890131

6

Point mutations at the carboxy terminus of the human dystrophin gene: implications for an association with mental retardation in DMD patients.

Lenk U, Hanke R, Thiele H, Speer A. Lenk U, et al. Hum Mol Genet. 1993 Nov;2(11):1877-81. doi: 10.1093/hmg/2.11.1877. Hum Mol Genet. 1993. PMID: 8281150

7

The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.

Koenig M, Beggs AH, Moyer M, Scherpf S, Heindrich K, Bettecken T, Meng G, Müller CR, Lindlöf M, Kaariainen H, de la Chapellet A, Kiuru A, Savontaus ML, Gilgenkrantz H, Récan D, Chelly J, Kaplan JC, Covone AE, Archidiacono N, Romeo G, Liechti-Gailati S, Schneider V, Braga S, Moser H, Darras BT, Murphy P, Francke U, Chen JD, Morgan G, Denton M, Greenberg CR, Wrogemann K, Blonden LA, van Paassen MB, van Ommen GJ, Kunkel LM. Koenig M, et al. Am J Hum Genet. 1989 Oct;45(4):498-506. Am J Hum Genet. 1989. PMID: 2491009 Free PMC article.

8

[Central nervous system involvements in Duchenne/Becker muscular dystrophy].

Kumagai T, Miura K, Ohki T, Matsumoto A, Miyazaki S, Nakamura M, Ochi N, Takahashi O. Kumagai T, et al. No To Hattatsu. 2001 Nov;33(6):480-6. No To Hattatsu. 2001. PMID: 11725514 Japanese.

9

Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) gene.

Gillard EF, Chamberlain JS, Murphy EG, Duff CL, Smith B, Burghes AH, Thompson MW, Sutherland J, Oss I, Bodrug SE, et al. Gillard EF, et al. Am J Hum Genet. 1989 Oct;45(4):507-20. Am J Hum Genet. 1989. PMID: 2491010 Free PMC article.

10

Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patients.

Dinçer P, Topaloğlu H, Ayter S, Ozgüç M, Taşdemir HA, Renda Y. Dinçer P, et al. Brain Dev. 1996 Mar-Apr;18(2):91-4. doi: 10.1016/0387-7604(95)00128-x. Brain Dev. 1996. PMID: 8733896 Clinical Trial.

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