105 related articles for article (PubMed ID: 1483993)
1. Changing clinical concepts of Duchenne muscular dystrophy: molecular genetic diagnosis.
Verma A; Maheshwari MC
J Assoc Physicians India; 1992 May; 40(5):324-5. PubMed ID: 1483993
[No Abstract] [Full Text] [Related]
2. Molecular genetics of Duchenne muscular dystrophy.
Tay J
J Singapore Paediatr Soc; 1990; 32(3-4):61-4. PubMed ID: 2133759
[No Abstract] [Full Text] [Related]
3. [The molecular principles of Duchenne and Becker muscular dystrophy and their genetic diagnosis].
Speer A; Davies KE; Hanke R; Grade K; Spiegler AW; Herrmann FH; Szibor R; Wulff K; Sommer D; Metzke H
Z Arztl Fortbild (Jena); 1989; 83(3):117-20. PubMed ID: 2655303
[No Abstract] [Full Text] [Related]
4. Molecular biology of Duchenne and Becker's muscular dystrophy: clinical applications.
Gutmann DH; Fischbeck KH
Ann Neurol; 1989 Aug; 26(2):189-94. PubMed ID: 2673003
[TBL] [Abstract][Full Text] [Related]
5. Congenital muscular dystrophy in a new age.
Day JW
Neurology; 2008 Jul; 71(5):308-9. PubMed ID: 18663176
[No Abstract] [Full Text] [Related]
6. [Diagnosis of Duchenne muscular dystrophy using DNA probes].
Evgrafov OV; Makarov VB
Zh Nevropatol Psikhiatr Im S S Korsakova; 1987; 87(11):1732-6. PubMed ID: 3324590
[No Abstract] [Full Text] [Related]
7. Molecular analysis of human muscular dystrophies.
Davies KE; Forrest S; Smith T; Kenwrick S; Ball S; Dorkins H; Patterson M
Muscle Nerve; 1987; 10(3):191-9. PubMed ID: 2882417
[TBL] [Abstract][Full Text] [Related]
8. The muscular dystrophies.
Seiler J; Bope ET
Am Fam Physician; 1986 Jul; 34(1):123-8. PubMed ID: 3728255
[TBL] [Abstract][Full Text] [Related]
9. [New aspects of carrier diagnosis and human genetic counseling in Duchenne and Becker muscular dystrophy].
Spiegler AW; Huppert P; Werner W; Metzke H; Strobel U; Köhler K; Gerhardt R; Kaufmann J; Herrmann FH
Z Arztl Fortbild (Jena); 1988; 82(22):1139-42. PubMed ID: 3247797
[No Abstract] [Full Text] [Related]
10. [Updates in muscular dystrophies].
Erazo-Torricelli R
Rev Neurol; 2004 Nov 1-15; 39(9):860-71. PubMed ID: 15543503
[TBL] [Abstract][Full Text] [Related]
11. Localization of the region homologous to the Duchenne muscular dystrophy locus on the mouse X chromosome.
Heilig R; Lemaire C; Mandel JL; Dandolo L; Amar L; Avner P
Nature; 1987 Jul 9-15; 328(6126):168-70. PubMed ID: 3600794
[TBL] [Abstract][Full Text] [Related]
12. [In which cases does molecular biology allow a diagnosis in neuromuscular pathology?].
Pouget J
Rev Neurol (Paris); 2009 Apr; 165 Spec No 2():F73-9. PubMed ID: 19593880
[No Abstract] [Full Text] [Related]
13. Possibilities and problems in genomic diagnosis of Duchenne muscular dystrophy with molecular probes.
Speer A; Davies K; McGlade S; Hanke R; Spiegler AW; Szibor R; Sommer D; Herrmann F; Coutelle C
Biomed Biochim Acta; 1986; 45(7):K19-27. PubMed ID: 2878658
[TBL] [Abstract][Full Text] [Related]
14. Does unequal crossing over contribute to the mutation rate in Duchenne muscular dystrophy?
Winter RM; Pembrey ME
Am J Med Genet; 1982 Aug; 12(4):437-41. PubMed ID: 7124796
[No Abstract] [Full Text] [Related]
15. Prenatal diagnosis of Duchenne and Becker muscular dystrophy.
Abbs S
Prenat Diagn; 1996 Dec; 16(13):1187-98. PubMed ID: 9061750
[TBL] [Abstract][Full Text] [Related]
16. The mapping of a cDNA from the human X-linked Duchenne muscular dystrophy gene to the mouse X chromosome.
Brockdorff N; Cross GS; Cavanna JS; Fisher EM; Lyon MF; Davies KE; Brown SD
Nature; 1987 Jul 9-15; 328(6126):166-8. PubMed ID: 3600793
[TBL] [Abstract][Full Text] [Related]
17. Molecular basis of neuromuscular diseases.
Chance PF; Ashizawa T; Hoffman EP; Crawford TO
Phys Med Rehabil Clin N Am; 1998 Feb; 9(1):49-81, vi. PubMed ID: 9894134
[TBL] [Abstract][Full Text] [Related]
18. Genetics of Duchenne muscular dystrophy.
Worton RG; Thompson MW
Annu Rev Genet; 1988; 22():601-29. PubMed ID: 3071259
[No Abstract] [Full Text] [Related]
19. Perspectives and molecular diagnosis of Duchenne and Becker muscular dystrophies.
Prior TW
Clin Lab Med; 1995 Dec; 15(4):927-41. PubMed ID: 8838231
[TBL] [Abstract][Full Text] [Related]
20. [Detection of deletions by the amplification of exons (multiplex PCR) in Duchenne muscular dystrophy].
Claustres M; Kjellberg P; Desgeorges M; Bellet H; Sarda P; Bonnet H; Boileau C
J Genet Hum; 1989 Sep; 37(3):251-7. PubMed ID: 2625628
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
