These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
160 related articles for article (PubMed ID: 7891372)
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 J Med Genet; 1994 Dec; 31(12):922-4. PubMed ID: 7891372 [TBL] [Abstract][Full Text] [Related]
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 Neuromuscul Disord; 1996 Aug; 6(4):275-81. PubMed ID: 8887957 [TBL] [Abstract][Full Text] [Related]
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 Hum Genet; 1996 Aug; 98(2):178-81. PubMed ID: 8698337 [TBL] [Abstract][Full Text] [Related]
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 Am J Hum Genet; 1995 May; 56(5):1108-15. PubMed ID: 7726166 [TBL] [Abstract][Full Text] [Related]
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 J Med Genet; 1990 May; 27(5):288-91. PubMed ID: 1972196 [TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of X-linked myotubular myopathy: strategies using new and tightly linked DNA markers. Hu LJ; Laporte J; Kress W; Dahl N Prenat Diagn; 1996 Mar; 16(3):231-7. PubMed ID: 8710776 [TBL] [Abstract][Full Text] [Related]
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 Genomics; 1996 May; 33(3):365-73. PubMed ID: 8660996 [TBL] [Abstract][Full Text] [Related]
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 Am J Hum Genet; 1992 Aug; 51(2):307-15. PubMed ID: 1642232 [TBL] [Abstract][Full Text] [Related]
11. Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304). Dahl N; Goonewardena P; Malmgren H; Gustavson KH; Holmgren G; Seemanova E; Annerén G; Flood A; Pettersson U Am J Hum Genet; 1989 Aug; 45(2):304-9. PubMed ID: 2569270 [TBL] [Abstract][Full Text] [Related]
12. 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 J Med Genet; 1990 May; 27(5):284-7. PubMed ID: 2352256 [TBL] [Abstract][Full Text] [Related]
13. Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28. Consalez GG; Stayton CL; Freimer NB; Goonewardena P; Brown WT; Gilliam TC; Warren ST Genomics; 1992 Apr; 12(4):710-4. PubMed ID: 1572645 [TBL] [Abstract][Full Text] [Related]
14. Deletions in Xq28 in two boys with myotubular myopathy and abnormal genital development define a new contiguous gene syndrome in a 430 kb region. Hu LJ; Laporte J; Kress W; Kioschis P; Siebenhaar R; Poustka A; Fardeau M; Metzenberg A; Janssen EA; Thomas N; Mandel JL; Dahl N Hum Mol Genet; 1996 Jan; 5(1):139-43. PubMed ID: 8789451 [TBL] [Abstract][Full Text] [Related]
15. X-linked nephrogenic diabetes insipidus: from the ship Hopewell to RFLP studies. Bichet DG; Hendy GN; Lonergan M; Arthus MF; Ligier S; Pausova Z; Kluge R; Zingg H; Saenger P; Oppenheimer E Am J Hum Genet; 1992 Nov; 51(5):1089-1102. PubMed ID: 1357965 [TBL] [Abstract][Full Text] [Related]
17. Genomic organization of a 225-kb region in Xq28 containing the gene for X-linked myotubular myopathy (MTM1) and a related gene (MTMR1). Kioschis P; Wiemann S; Heiss NS; Francis F; Götz C; Poustka A; Taudien S; Platzer M; Wiehe T; Beckmann G; Weber J; Nordsiek G; Rosenthal A Genomics; 1998 Dec; 54(2):256-66. PubMed ID: 9828128 [TBL] [Abstract][Full Text] [Related]
18. A new polymorphic marker very closely linked to DXS52 in the q28 region of the human X chromosome. Vincent A; Kretz C; Oberlé I; Mandel JL Hum Genet; 1989 Apr; 82(1):85-6. PubMed ID: 2565870 [TBL] [Abstract][Full Text] [Related]