301 related articles for article (PubMed ID: 9503753)
1. Clinical expression of myotonic dystrophy: the predictive role of DNA diagnosis.
Can B; Schaefer FV; Malik S; Floyd M; Say B
J Okla State Med Assoc; 1998; 91(1):7-10. PubMed ID: 9503753
[TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis of congenital myotonic dystrophy and counseling of the pregnant mother: case report and literature review.
Geifman-Holtzman O; Fay K
Am J Med Genet; 1998 Jul; 78(3):250-3. PubMed ID: 9677060
[TBL] [Abstract][Full Text] [Related]
3. "Shake hands"; diagnosing a floppy infant--myotonic dystrophy and the congenital subtype: a difficult perinatal diagnosis.
Verrijn Stuart AA; Huisman M; van Straaten HL; Bakker JC; Arabin B
J Perinat Med; 2000; 28(6):497-501. PubMed ID: 11155437
[TBL] [Abstract][Full Text] [Related]
4. [Steinert's disease and pregnancy. A case report and recent literature].
Delest A; Elhage A; Cosson M; Leclercq G; Gremillet C; Pasquier F; Manouvrier-Hanu S; Decocq J; Delahousse G
J Gynecol Obstet Biol Reprod (Paris); 1995; 24(2):177-80. PubMed ID: 7782590
[TBL] [Abstract][Full Text] [Related]
5. [Clinical, familial and hereditary analysis of myotonic dystrophy].
Wu Z; Yang J; Cao J; Hu Z; Zhan Y; Li J; Li Y; Wang Y; Zhang C
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2011 Jun; 36(6):520-4. PubMed ID: 21743143
[TBL] [Abstract][Full Text] [Related]
6. [Molecular genetics diagnosis of Steinert's myotonic dystrophy].
Spiegel R; Einschenk I; Schinzel A; Shelbourne P; Johnson K; Boltshauser E; Schmid W
Schweiz Med Wochenschr; 1992 Oct; 122(42):1553-8. PubMed ID: 1411415
[TBL] [Abstract][Full Text] [Related]
7. Clinical application of preimplantation diagnosis for myotonic dystrophy.
Sermon K; Lissens W; Joris H; Seneca S; Desmyttere S; Devroey P; Van Steirteghem A; Liebaers I
Prenat Diagn; 1997 Oct; 17(10):925-32. PubMed ID: 9358572
[TBL] [Abstract][Full Text] [Related]
8. DNA analysis in a suspected individual with myotonic dystrophy family history and her abortus.
Bi X; Xie H; Zheng H; Ding S; Zhang S; Wang Y; Xu Z; Ren D
Chin Med J (Engl); 2002 Nov; 115(11):1628-31. PubMed ID: 12609075
[TBL] [Abstract][Full Text] [Related]
9. Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspring.
Redman JB; Fenwick RG; Fu YH; Pizzuti A; Caskey CT
JAMA; 1993 Apr; 269(15):1960-5. PubMed ID: 8464127
[TBL] [Abstract][Full Text] [Related]
10. Myotonic dystrophy: molecular genetics and diagnosis.
Gharehbaghi-Schnell E; Finsterer J; Korschineck I; Mamoli B; Binder BR
Wien Klin Wochenschr; 1998 Jan; 110(1):7-14. PubMed ID: 9499472
[TBL] [Abstract][Full Text] [Related]
11. [Clinical and molecular genetic analyses of congenital myotonic dystrophy].
Kojo T; Arahata K
Nihon Rinsho; 1997 Dec; 55(12):3234-8. PubMed ID: 9436443
[TBL] [Abstract][Full Text] [Related]
12. Congenital myotonic dystrophy: molecular diagnosis and clinical study.
Hojo K; Yamagata H; Moji H; Fujita T; Miki T; Fujimura M; Kidoguchi K
Am J Perinatol; 1995 May; 12(3):195-200. PubMed ID: 7612095
[TBL] [Abstract][Full Text] [Related]
13. Sleep apnea and respiratory dysfunction in congenital myotonic dystrophy.
Avanzini A; Crossignani RM; Colombini A
Minerva Pediatr; 2001 Jun; 53(3):221-5. PubMed ID: 11455309
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis in myotonic dystrophy type 1. Thirteen years of experience: implications for reproductive counselling in DM1 families.
Martorell L; Cobo AM; Baiget M; Naudó M; Poza JJ; Parra J
Prenat Diagn; 2007 Jan; 27(1):68-72. PubMed ID: 17154336
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis for the unstable CTG repeat sequence in myotonic dystrophy: a retrospective study in a French family.
Lucotte G; Berriche S; David F; Mariotti M; Turpin JC
Genet Couns; 1994; 5(2):171-4. PubMed ID: 7917127
[TBL] [Abstract][Full Text] [Related]
16. Molecular analysis of the CTG trinucleotide repeat in South African myotonic dystrophy families--implications for diagnosis and counselling.
Goldman A; Ramsay M; Jenkins T
S Afr Med J; 1995 Nov; 85(11):1161-4. PubMed ID: 8597005
[TBL] [Abstract][Full Text] [Related]
17. [Dystrophia myotonica and pregnancy].
van de Biezenbos JB; Nijhuis JG; Brunner HG
Ned Tijdschr Geneeskd; 1992 Dec; 136(50):2480-2. PubMed ID: 1465172
[TBL] [Abstract][Full Text] [Related]
18. Five years experience of predictive testing for myotonic dystrophy using linked DNA markers.
Reardon W; Floyd JL; Myring J; Lazarou LP; Meredith AL; Harper PS
Am J Med Genet; 1992 Aug; 43(6):1006-11. PubMed ID: 1415325
[TBL] [Abstract][Full Text] [Related]
19. Direct diagnosis of myotonic dystrophy with a disease-specific DNA marker.
Shelbourne P; Davies J; Buxton J; Anvret M; Blennow E; Bonduelle M; Schmedding E; Glass I; Lindenbaum R; Lane R
N Engl J Med; 1993 Feb; 328(7):471-5. PubMed ID: 8421476
[TBL] [Abstract][Full Text] [Related]
20. [Genetic counseling in myotonia and muscular dystrophy].
Becker PE
Internist (Berl); 1978 Aug; 19(8):475-81. PubMed ID: 357337
[No Abstract] [Full Text] [Related]
[Next] [New Search]
