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.
91 related articles for article (PubMed ID: 6140416)
1. Duchenne muscular dystrophy: carrier detection by ultrasound and computerised tomography. Rott HD; Santellani M; Breimesser FH Lancet; 1984 Jan; 1(8368):111. PubMed ID: 6140416 [No Abstract] [Full Text] [Related]
2. Duchenne muscular dystrophy: carrier detection by ultrasound and computerised tomography. Rott HD; Santellani M; Rödl W; Nebel G Lancet; 1983 Nov; 2(8360):1199-200. PubMed ID: 6139557 [No Abstract] [Full Text] [Related]
3. Duchenne muscular dystrophy: carrier detection by ultrasound. Steinbicker V; von Rohden L; Krebs P; Szibor R Lancet; 1984 Jun; 1(8392):1463. PubMed ID: 6145895 [No Abstract] [Full Text] [Related]
4. Detecting the Duchenne carrier by ultrasound and computerized tomography. Heckmatt JZ; Dubowitz V Lancet; 1983 Dec; 2(8363):1364. PubMed ID: 6139695 [No Abstract] [Full Text] [Related]
5. Carrier detection of Duchenne muscular dystrophy by computerised tomography. Castro-Gago M; Alonso A; Novo I; Fuster M Lancet; 1986 May; 1(8488):1039. PubMed ID: 2871322 [No Abstract] [Full Text] [Related]
6. Duchenne muscular dystrophy. Use of rubidium chloride Rb 86 in the detection of carriers of the gene. Bradley WG; Gardner-Medwin D; Haggith J; Walton JN; Hesp R Arch Neurol; 1971 Sep; 25(3):193-7. PubMed ID: 4951942 [No Abstract] [Full Text] [Related]
7. Computed tomographic findings in manifesting carriers of Duchenne muscular dystrophy. de Visser M; Verbeeten B Clin Genet; 1985 Mar; 27(3):269-75. PubMed ID: 3987077 [TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis of Duchenne muscular dystrophy by DNA analysis. Old JM; Davies KE J Med Genet; 1986 Dec; 23(6):556-9. PubMed ID: 2879927 [TBL] [Abstract][Full Text] [Related]
10. The use of flanking markers in prediction for Duchenne muscular dystrophy. Williams H; Sarfarazi M; Brown C; Thomas N; Harper PS Arch Dis Child; 1986 Mar; 61(3):218-22. PubMed ID: 3457554 [TBL] [Abstract][Full Text] [Related]
11. Direct diagnosis of carriers of point mutations in Duchenne muscular dystrophy. Yau SC; Roberts RG; Bobrow M; Mathew CG Lancet; 1993 Jan; 341(8840):273-5. PubMed ID: 8093919 [TBL] [Abstract][Full Text] [Related]
12. Lymphocyte capping and carrier detection in Duchenne muscular dystrophy. Br Med J; 1978 Dec; 2(6152):1589-90. PubMed ID: 728736 [No Abstract] [Full Text] [Related]
13. Determination of Duchenne muscular dystrophy carrier status by single strand conformation polymorphism analysis of deleted regions of the dystrophin locus. Richards RI; Friend K J Med Genet; 1991 Dec; 28(12):856-9. PubMed ID: 1757962 [TBL] [Abstract][Full Text] [Related]
14. DNA probes for carrier identification in Duchenne muscular dystrophy. Worton RG Clin Chem; 1989 Apr; 35(4):519-20. PubMed ID: 2564816 [No Abstract] [Full Text] [Related]