Similar articles for PMID: 7891372

Year	Number of Results
1975	1
1984	2
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1989	4
1990	8
1991	13
1992	6
1993	13
1994	13
1995	8
1996	12
1997	7
1998	7
1999	5
2000	1
2002	1
2003	2
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2017	2
2019	1
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2024	0

1

X linked myotubular myopathy (MTM1) maps between DXS304 and DXS305, closely linked to the DXS455 VNTR and a new, highly informative microsatellite marker (DXS1684).

Dahl N, Samson F, Thomas NS, Hu LJ, Gong W, Herman G, Laporte J, Kioschis P, Poustka A, Mandel JL. Dahl N, et al. J Med Genet. 1994 Dec;31(12):922-4. doi: 10.1136/jmg.31.12.922. J Med Genet. 1994. PMID: 7891372 Free PMC article.

2

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.

3

X-linked myotubular myopathy: refinement of the gene to a 280-kb region with new and highly informative microsatellite markers.

Hu LJ, Laporte J, Kioschis P, Heyberger S, Kretz C, Poustka A, Mandel JL, Dahi N. Hu LJ, et al. Hum Genet. 1996 Aug;98(2):178-81. doi: 10.1007/s004390050185. Hum Genet. 1996. PMID: 8698337

4

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.

5

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.

6

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.

7

Prenatal diagnosis of X-linked myotubular myopathy: strategies using new and tightly linked DNA markers.

Hu LJ, Laporte J, Kress W, Dahl N. Hu LJ, et al. Prenat Diagn. 1996 Mar;16(3):231-7. doi: 10.1002/(SICI)1097-0223(199603)16:3<231::AID-PD842>3.0.CO;2-M. Prenat Diagn. 1996. PMID: 8710776

8

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

9

A 900-kb cosmid contig and 10 new transcripts within the candidate region for myotubular myopathy (MTM1).

Kioschis P, Rogner UC, Pick E, Klauck SM, Heiss N, Siebenhaar R, Korn B, Coy JF, Laporte J, Liechti-Gallati S, Poustka A. Kioschis P, et al. Genomics. 1996 May 1;33(3):365-73. doi: 10.1006/geno.1996.0212. Genomics. 1996. PMID: 8660996

10

Further localization of X-linked hydrocephalus in the chromosomal region Xq28.

Willems PJ, Vits L, Raeymaekers P, Beuten J, Coucke P, Holden JJ, Van Broeckhoven C, Warren ST, Sagi M, Robinson D, et al. Willems PJ, et al. Am J Hum Genet. 1992 Aug;51(2):307-15. Am J Hum Genet. 1992. PMID: 1642232 Free PMC article.

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