Similar articles for PMID: 7881289

Year	Number of Results
1984	3
1985	1
1986	1
1987	4
1988	2
1989	4
1990	8
1991	16
1992	9
1993	7
1994	4
1995	8
1996	9
1997	5
1998	5
1999	3
2000	2
2001	2
2003	1
2007	1
2013	1
2020	1
2021	1
2024	0

1

The gene for X-linked myotubular myopathy is located in an 8 Mb region at the border of Xq27.3 and Xq28.

Janssen EA, Hensels GW, van Oost BA, Hamel BC, Kemp S, Baas F, Weber JW, Barth PG, Bolhuis PA. Janssen EA, et al. Neuromuscul Disord. 1994 Sep-Nov;4(5-6):455-61. doi: 10.1016/0960-8966(94)90084-1. Neuromuscul Disord. 1994. PMID: 7881289

2

X linked neonatal centronuclear/myotubular myopathy: evidence for linkage to Xq28 DNA marker loci.

Thomas NS, Williams H, Cole G, Roberts K, Clarke A, Liechti-Gallati S, Braga S, Gerber A, Meier C, Moser H, et al. Thomas NS, et al. J Med Genet. 1990 May;27(5):284-7. doi: 10.1136/jmg.27.5.284. J Med Genet. 1990. PMID: 2352256 Free PMC article.

3

X linked neonatal myotubular myopathy: one recombination detected with four polymorphic DNA markers from Xq28.

Lehesjoki AE, Sankila EM, Miao J, Somer M, Salonen R, Rapola J, de la Chapelle A. Lehesjoki AE, et al. J Med Genet. 1990 May;27(5):288-91. doi: 10.1136/jmg.27.5.288. J Med Genet. 1990. PMID: 1972196 Free PMC article.

4

Genetic linkage heterogeneity in myotubular myopathy.

Samson F, Mesnard L, Heimburger M, Hanauer A, Chevallay M, Mercadier JJ, Pelissier JF, Feingold N, Junien C, Mandel JL, et al. Samson F, et al. Am J Hum Genet. 1995 Jul;57(1):120-6. Am J Hum Genet. 1995. PMID: 7611280 Free PMC article.

5

Genetic mapping of new RFLPs at Xq27-q28.

Suthers GK, Oberlé I, Nancarrow J, Mulley JC, Hyland VJ, Wilson PJ, McCure J, Morris CP, Hopwood JJ, Mandel JL, et al. Suthers GK, et al. Genomics. 1991 Jan;9(1):37-43. doi: 10.1016/0888-7543(91)90218-4. Genomics. 1991. PMID: 1672291

6

X-linked myotubular myopathy: refinement of the critical gene region.

Smolenicka Z, Laporte J, Hu L, Dahl N, Fitzpatrick J, Kress W, Liechti-Gallati S. Smolenicka Z, et al. Neuromuscul Disord. 1996 Aug;6(4):275-81. doi: 10.1016/0960-8966(96)00364-1. Neuromuscul Disord. 1996. PMID: 8887957 Review.

7

X-linked centronuclear myopathy: mapping the gene to Xq28.

Liechti-Gallati S, Müller B, Grimm T, Kress W, Müller C, Boltshauser E, Moser H, Braga S. Liechti-Gallati S, et al. Neuromuscul Disord. 1991;1(4):239-45. doi: 10.1016/0960-8966(91)90096-b. Neuromuscul Disord. 1991. PMID: 1822801

8

Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28.

Bolhuis PA, Hensels GW, Hulsebos TJ, Baas F, Barth PG. Bolhuis PA, et al. Am J Hum Genet. 1991 Mar;48(3):481-5. Am J Hum Genet. 1991. PMID: 1998334 Free PMC article.

9

The gene for X-linked hydrocephalus maps to Xq28, distal to DXS52.

Lyonnet S, Pelet A, Royer G, Delrieu O, Serville F, le Marec B, Gruensteudel A, Pfeiffer RA, Briard ML, Dubay C, et al. Lyonnet S, et al. Genomics. 1992 Oct;14(2):508-10. doi: 10.1016/s0888-7543(05)80254-x. Genomics. 1992. PMID: 1427869

10

Myotubular myopathy in a girl with a deletion at Xq27-q28 and unbalanced X inactivation assigns the MTM1 gene to a 600-kb region.

Dahl N, Hu LJ, Chery M, Fardeau M, Gilgenkrantz S, Nivelon-Chevallier A, Sidaner-Noisette I, Mugneret F, Gouyon JB, Gal A, et al. Dahl N, et al. Am J Hum Genet. 1995 May;56(5):1108-15. Am J Hum Genet. 1995. PMID: 7726166 Free PMC article.

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