Similar articles for PMID: 8710776

Year	Number of Results
1968	1
1969	1
1974	1
1978	1
1980	2
1983	1
1984	3
1986	2
1987	1
1988	3
1989	5
1990	7
1991	3
1992	4
1993	15
1994	9
1995	13
1996	13
1997	8
1998	11
1999	8
2000	5
2001	1
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2003	3
2005	5
2006	3
2007	2
2008	3
2009	3
2010	1
2015	1
2017	1
2019	1
2021	2
2024	0

1

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

2

Confirmation of prenatal diagnosis results of X-linked recessive myotubular myopathy by mutational screening, and description of three new mutations in the MTM1 gene.

Tanner SM, Laporte J, Guiraud-Chaumeil C, Liechti-Gallati S. Tanner SM, et al. Hum Mutat. 1998;11(1):62-8. doi: 10.1002/(SICI)1098-1004(1998)11:1<62::AID-HUMU10>3.0.CO;2-X. Hum Mutat. 1998. PMID: 9450905

3

Prenatal diagnosis of X-linked centronuclear myopathy by linkage analysis.

Liechti-Gallati S, Wolff G, Ketelsen UP, Braga S. Liechti-Gallati S, et al. Pediatr Res. 1993 Feb;33(2):201-4. doi: 10.1203/00006450-199302000-00022. Pediatr Res. 1993. PMID: 8433896

4

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

5

Genomic organization of the MTM1 gene implicated in X-linked myotubular myopathy.

Laporte J, Guiraud-Chaumeil C, Tanner SM, Blondeau F, Hu LJ, Vicaire S, Liechti-Gallati S, Mandel JL. Laporte J, et al. Eur J Hum Genet. 1998 Jul-Aug;6(4):325-30. doi: 10.1038/sj.ejhg.5200189. Eur J Hum Genet. 1998. PMID: 9781038

6

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.

7

A gene mutated in X-linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast.

Laporte J, Hu LJ, Kretz C, Mandel JL, Kioschis P, Coy JF, Klauck SM, Poustka A, Dahl N. Laporte J, et al. Nat Genet. 1996 Jun;13(2):175-82. doi: 10.1038/ng0696-175. Nat Genet. 1996. PMID: 8640223

8

Linkage of X-linked myopathy with excessive autophagy (XMEA) to Xq28.

Villard L, des Portes V, Levy N, Louboutin JP, Recan D, Coquet M, Chabrol B, Figarella-Branger D, Chelly J, Pellissier JF, Fontes M. Villard L, et al. Eur J Hum Genet. 2000 Feb;8(2):125-9. doi: 10.1038/sj.ejhg.5200432. Eur J Hum Genet. 2000. PMID: 10757644

9

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

10

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.

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