109 related articles for article (PubMed ID: 8433896)
1. Prenatal diagnosis of X-linked centronuclear myopathy by linkage analysis.
Liechti-Gallati S; Wolff G; Ketelsen UP; Braga S
Pediatr Res; 1993 Feb; 33(2):201-4. PubMed ID: 8433896
[TBL] [Abstract][Full Text] [Related]
2. 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
Neuromuscul Disord; 1991; 1(4):239-45. PubMed ID: 1822801
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Severe neonatal centronuclear (myotubular) myopathy: an X-linked recessive disorder.
Bucher HU; Boltshauser E; Briner J; Gnehm HE; Janzer RC
Helv Paediatr Acta; 1986 Oct; 41(4):291-300. PubMed ID: 3793508
[TBL] [Abstract][Full Text] [Related]
5. 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
Hum Mutat; 1998; 11(1):62-8. PubMed ID: 9450905
[TBL] [Abstract][Full Text] [Related]
6. Centronuclear (myotubular) myopathy.
Jungbluth H; Wallgren-Pettersson C; Laporte J
Orphanet J Rare Dis; 2008 Sep; 3():26. PubMed ID: 18817572
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of X-linked hypohidrotic ectodermal dysplasia by linkage analysis.
Zonana J; Schinzel A; Upadhyaya M; Thomas NS; Anton-Lamprecht I; Harper PS
Am J Med Genet; 1990 Jan; 35(1):132-5. PubMed ID: 2301463
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. A linkage study of a large pedigree with X linked centronuclear myopathy.
Starr J; Lamont M; Iselius L; Harvey J; Heckmatt J
J Med Genet; 1990 May; 27(5):281-3. PubMed ID: 2352255
[TBL] [Abstract][Full Text] [Related]
10. X-linked myotubular myopathy: clinical observations in ten additional cases.
Joseph M; Pai GS; Holden KR; Herman G
Am J Med Genet; 1995 Nov; 59(2):168-73. PubMed ID: 8588581
[TBL] [Abstract][Full Text] [Related]
11. 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
Am J Hum Genet; 1995 Jul; 57(1):120-6. PubMed ID: 7611280
[TBL] [Abstract][Full Text] [Related]
12. Non-invasive first trimester fetal gender assignment in pregnancies at risk for X-linked recessive diseases.
Mazza V; Falcinelli C; Percesepe A; Paganelli S; Volpe A; Forabosco A
Prenat Diagn; 2002 Oct; 22(10):919-24. PubMed ID: 12378578
[TBL] [Abstract][Full Text] [Related]
13. X-linked recessive myotubular myopathy proven by muscle biopsy.
Tsai CH; Huang WS; Tsai FJ; Lee CC; Chen SS
J Formos Med Assoc; 1996 Feb; 95(2):153-6. PubMed ID: 9064005
[TBL] [Abstract][Full Text] [Related]
14. Severe neonatal asphyxia due to X-linked centronuclear myopathy.
Braga SE; Gerber A; Meier C; Weiersmüller A; Zimmermann A; Herrmann U; Liechti S; Moser H
Eur J Pediatr; 1990 Dec; 150(2):132-5. PubMed ID: 2279510
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Prenatal diagnosis of cystic fibrosis by using linked DNA markers in 138 pregnancies at 1-in-4 risk.
Feldman GL; Lewiston N; Fernbach SD; O'Brien WE; Williamson R; Wainwright BJ; Beaudet AL
Am J Med Genet; 1989 Jun; 33(2):238-41. PubMed ID: 2569827
[TBL] [Abstract][Full Text] [Related]
17. X-linked centronuclear myopathy as a cause of floppy baby.
Donders G; Moerman P; Devlieger H; Spitz B; Van Assche FA
Eur J Obstet Gynecol Reprod Biol; 1987 Jan; 24(1):33-8. PubMed ID: 3817270
[TBL] [Abstract][Full Text] [Related]
18. 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
Eur J Hum Genet; 2000 Feb; 8(2):125-9. PubMed ID: 10757644
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): molecular genetics, clinical experience, and fetal morphology.
Zerres K; Mücher G; Becker J; Steinkamm C; Rudnik-Schöneborn S; Heikkilä P; Rapola J; Salonen R; Germino GG; Onuchic L; Somlo S; Avner ED; Harman LA; Stockwin JM; Guay-Woodford LM
Am J Med Genet; 1998 Mar; 76(2):137-44. PubMed ID: 9511976
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis and detection of carriers with DNA probes in Duchenne's muscular dystrophy.
Darras BT; Harper JF; Francke U
N Engl J Med; 1987 Apr; 316(16):985-92. PubMed ID: 3561454
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
