165 related articles for article (PubMed ID: 6842530)
1. The genetic status of mothers of isolated cases of Duchenne muscular dystrophy.
Lane RJ; Robinow M; Roses AD
J Med Genet; 1983 Feb; 20(1):1-11. PubMed ID: 6842530
[TBL] [Abstract][Full Text] [Related]
2. Frequency of new mutants among boys with Duchenne muscular dystrophy.
Bucher K; Ionasescu V; Hanson J
Am J Med Genet; 1980; 7(1):27-34. PubMed ID: 7211951
[TBL] [Abstract][Full Text] [Related]
3. Gene studies in newborn males with Duchenne muscular dystrophy detected by neonatal screening.
Greenberg CR; Rohringer M; Jacobs HK; Averill N; Nylen E; van Ommen GJ; Wrogemann K
Lancet; 1988 Aug; 2(8608):425-7. PubMed ID: 2900355
[TBL] [Abstract][Full Text] [Related]
4. Sporadic occurrence of Duchenne muscular dystrophy: evidence for new mutation.
Caskey CT; Nussbaum RL; Cohan LC; Pollack L
Clin Genet; 1980 Nov; 18(5):329-41. PubMed ID: 7460369
[TBL] [Abstract][Full Text] [Related]
5. DUCHEN: an interactive computer program for calculating heterozygosity (carrier) risks in X-linked recessive lethal diseases, and its application in Duchenne muscular dystrophy.
Andrews DF; Brasher PM; Manchester KE; Percy ME; Rusk AC; Soltan HC; Trueman DW
Am J Med Genet; 1986 Oct; 25(2):211-8. PubMed ID: 3777018
[TBL] [Abstract][Full Text] [Related]
6. Carrier testing in families of isolated cases of duchenne muscular dystrophy. Creatine kinase activities in female relatives of mothers with normal CK activity.
Nicholson GA; Lane RJ; Gardner-Medwin D; Walton JN
J Neurol Sci; 1981 Jul; 51(1):29-42. PubMed ID: 7252519
[TBL] [Abstract][Full Text] [Related]
7. [Carrier diagnosis and prenatal prognosis using DNA analysis in X-chromosome-linked Duchenne and Becker muscular dystrophy].
Moser H; Liechti-Gallati S; Braga S; Hirsiger H
Schweiz Med Wochenschr; 1987 Dec; 117(51):2061-73. PubMed ID: 3433090
[TBL] [Abstract][Full Text] [Related]
8. Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.
Lindlöf M; Kääriäinen H; Davies KE; de la Chapelle A
J Med Genet; 1986 Dec; 23(6):560-72. PubMed ID: 2879928
[TBL] [Abstract][Full Text] [Related]
9. Lactate dehydrogenase isoenzyme in detecting carriers of Duchenne muscular dystrophy.
Roses AD; Roses MJ; Nicholson GA; Roe CR
Neurology; 1977 May; 27(5):414-21. PubMed ID: 558544
[TBL] [Abstract][Full Text] [Related]
10. DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.
Bakker E; Bonten EJ; De Lange LF; Veenema H; Majoor-Krakauer D; Hofker MH; Van Ommen GJ; Pearson PL
J Med Genet; 1986 Dec; 23(6):573-80. PubMed ID: 2879929
[TBL] [Abstract][Full Text] [Related]
11. Use of DNA probes in detecting carriers of Duchenne muscular dystrophy: selected case studies.
Prior TW; Blasco PA; Dove JL; Leshner RT; Gruemer HD
Clin Chem; 1989 Apr; 35(4):679-83. PubMed ID: 2564818
[TBL] [Abstract][Full Text] [Related]
12. Genetic counseling of isolated carriers of Duchenne muscular dystrophy.
Hoffman EP; Pegoraro E; Scacheri P; Burns RG; Taber JW; Weiss L; Spiro A; Blattner P
Am J Med Genet; 1996 Jun; 63(4):573-80. PubMed ID: 8826437
[TBL] [Abstract][Full Text] [Related]
13. Pedigree testing in Duchenne muscular dystrophy.
Roses AD; Roses MJ; Metcalf BS; Hull KL; Nicholson GA; Hartwig GB; Roe CR
Ann Neurol; 1977 Oct; 2(4):271-8. PubMed ID: 617266
[TBL] [Abstract][Full Text] [Related]
14. Decreased incidence of Duchenne muscular dystrophy in western Japan 1956-1980.
Takeshita K; Kasagi S; Mito T; Tanaka T; Ootani K
Neuroepidemiology; 1987; 6(3):130-8. PubMed ID: 3658082
[TBL] [Abstract][Full Text] [Related]
15. Germline mosaicism and Duchenne muscular dystrophy mutations.
Bakker E; Van Broeckhoven C; Bonten EJ; van de Vooren MJ; Veenema H; Van Hul W; Van Ommen GJ; Vandenberghe A; Pearson PL
Nature; 1987 Oct 8-14; 329(6139):554-6. PubMed ID: 2889144
[TBL] [Abstract][Full Text] [Related]
16. [Newborn screening for Duchenne muscular dystrophy (author's transl)].
Grimm T
Monatsschr Kinderheilkd; 1981 Jul; 129(7):414-7. PubMed ID: 6115310
[TBL] [Abstract][Full Text] [Related]
17. Service experience using DNA analysis for genetic prediction in Duchenne muscular dystrophy.
Goodship J; Malcolm S; Robertson ME; Pembrey ME
J Med Genet; 1988 Jan; 25(1):14-9. PubMed ID: 2895187
[TBL] [Abstract][Full Text] [Related]
18. Duchenne muscular dystrophy in Wales: a 15 year study, 1971 to 1986.
Norman AM; Rogers C; Sibert JR; Harper PS
J Med Genet; 1989 Sep; 26(9):560-4. PubMed ID: 2810339
[TBL] [Abstract][Full Text] [Related]
19. Increase in fetal breech presentation in female carriers of Duchenne muscular dystrophy.
Geifman-Holtzman O; Bernstein IM; Capeless EL; Hawley P; Specht LA; Bianchi DW
Am J Med Genet; 1997 Dec; 73(3):276-8. PubMed ID: 9415684
[TBL] [Abstract][Full Text] [Related]
20. [Use of dystrophin c-DNA for the direct diagnosis of Duchenne muscular dystrophy in female carriers].
Baiget M; del Río E; Gallano P
Neurologia; 1989 Oct; 4(8):268-76. PubMed ID: 2576910
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]