193 related articles for article (PubMed ID: 6310392)
1. Recombinant DNA strategies in genetic neurological diseases.
Roses AD; Pericak-Vance MA; Yamaoka LH; Stubblefield E; Stajich J; Vance JM; Roses MJ; Carter DB
Muscle Nerve; 1983 Jun; 6(5):339-55. PubMed ID: 6310392
[TBL] [Abstract][Full Text] [Related]
2. Molecular genetics, recombinant DNA techniques, and genetic neurological disease.
Rosenberg RN
Ann Neurol; 1984 Jun; 15(6):511-20. PubMed ID: 6378063
[TBL] [Abstract][Full Text] [Related]
3. Molecular genetic strategies to investigate Huntington's disease.
Gilliam TC; Gusella JF; Lehrach H
Adv Neurol; 1988; 48():17-29. PubMed ID: 2891255
[No Abstract] [Full Text] [Related]
4. [Diagnostic studies in patients and relatives with hereditary neuromuscular diseases].
Moser H
Ther Umsch; 1995 Dec; 52(12):810-3. PubMed ID: 8539652
[TBL] [Abstract][Full Text] [Related]
5. Inherited neuropathies: Charcot-Marie-Tooth disease and related disorders.
Chance PF; Lupski JR
Baillieres Clin Neurol; 1994 Aug; 3(2):373-85. PubMed ID: 7952853
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [Clinico-genalogic characteristics of hereditary diseases of the nervous system in the Kuibyshev region].
Nesterov LN; Sushcheva GP; Viatkina SIa
Zh Nevropatol Psikhiatr Im S S Korsakova; 1978; 78(10):1506-12. PubMed ID: 152555
[TBL] [Abstract][Full Text] [Related]
8. [Neurogenetics. Part 3. New developments in gene mapping and diagnosis].
Gasser T; Meitinger T
Nervenarzt; 1993 Jun; 64(6):353-9. PubMed ID: 8332227
[TBL] [Abstract][Full Text] [Related]
9. Molecular genetics of neurodegenerative diseases.
Roses AD
Curr Opin Neurol Neurosurg; 1993 Feb; 6(1):34-9. PubMed ID: 8428064
[TBL] [Abstract][Full Text] [Related]
10. Molecular genetic approaches to the analysis of inherited neurological disease.
Cooper DN
Ann Clin Res; 1986; 18(5-6):264-70. PubMed ID: 2882729
[No Abstract] [Full Text] [Related]
11. [Neurogenetics--the challenge for neurology. 1. Neurogenetic diseases].
Gasser T; Trenkwalder C; Meitinger T; Witt TN; Murken J; Oertel WH
Nervenarzt; 1991 Oct; 62(10):590-608. PubMed ID: 1749451
[TBL] [Abstract][Full Text] [Related]
12. The application of recombinant DNA methodology to the diagnosis of inherited disease.
Cooper DN
Contrib Gynecol Obstet; 1986; 15():90-103. PubMed ID: 3017631
[No Abstract] [Full Text] [Related]
13. The muscular dystrophies.
Bushby KM
Baillieres Clin Neurol; 1994 Aug; 3(2):407-30. PubMed ID: 7952855
[TBL] [Abstract][Full Text] [Related]
14. Gene mapping and myotonic dystrophy.
Harper PS; Shaw D; Meredith L; Sarfarazi M; Brook D; Huson S
Prog Clin Biol Res; 1985; 177():61-76. PubMed ID: 2989839
[No Abstract] [Full Text] [Related]
15. Direct molecular genetic diagnosis and heterozygote identification in X-linked Emery-Dreifuss muscular dystrophy by heteroduplex analysis.
Wulff K; Ebener U; Wehnert CS; Ward PA; Reuner U; Hiebsch W; Herrmann FH; Wehnert M
Dis Markers; 1997 Apr; 13(2):77-86. PubMed ID: 9160182
[TBL] [Abstract][Full Text] [Related]
16. [The genetic basis of muscle disease].
Bindoff L; Gilhus NE
Tidsskr Nor Laegeforen; 2003 Sep; 123(18):2588-92. PubMed ID: 14714051
[TBL] [Abstract][Full Text] [Related]
17. DNA diagnostic tests in Xp21 dystrophy families for prenatal diagnosis.
Dinçer P; Topaloğlu H; Ayter S
Turk J Pediatr; 1998; 40(3):347-55. PubMed ID: 9763898
[TBL] [Abstract][Full Text] [Related]
18. [Molecular genetics of inherited neuropathies].
Takashima H
Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
[TBL] [Abstract][Full Text] [Related]
19. Screening for genetic diseases with molecular probes.
Davies KA; Williamson R
Ann Biol Clin (Paris); 1986; 44(2):112-5. PubMed ID: 3530062
[TBL] [Abstract][Full Text] [Related]
20. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]