144 related articles for article (PubMed ID: 2995673)
1. New perspectives for the elucidation of genetic disorders.
Ropers HH
Am J Hum Genet; 2007 Aug; 81(2):199-207. PubMed ID: 17668371
[TBL] [Abstract][Full Text] [Related]
2. The human Y chromosome.
Goodfellow P; Darling S; Wolfe J
J Med Genet; 1985 Oct; 22(5):329-44. PubMed ID: 3908683
[TBL] [Abstract][Full Text] [Related]
3. Isolation of a conserved sequence deleted in Duchenne muscular dystrophy patients.
Smith TJ; Wilson L; Kenwrick SJ; Forrest SM; Speer A; Coutelle C; Davies KE
Nucleic Acids Res; 1987 Mar; 15(5):2167-74. PubMed ID: 3562224
[TBL] [Abstract][Full Text] [Related]
4. A multipoint linkage analysis program for X-linked disorders, with the example of Duchenne muscular dystrophy and seven DNA probes.
Clayton J
Hum Genet; 1986 May; 73(1):68-72. PubMed ID: 3458666
[TBL] [Abstract][Full Text] [Related]
5. Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy families.
Dorkins H; Junien C; Mandel JL; Wrogemann K; Moison JP; Martinez M; Old JM; Bundey S; Schwartz M; Carpenter N
Hum Genet; 1985; 71(2):103-7. PubMed ID: 2995231
[TBL] [Abstract][Full Text] [Related]
6. Isolation of the gene for Duchenne muscular dystrophy.
Singh DN
Indian J Pediatr; 1988; 55(2):177-82. PubMed ID: 2900215
[No Abstract] [Full Text] [Related]
7. 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]
8. Gene mapping of mineral metabolic disorders.
Thakker RV; Davies KE; O'Riordan JL
J Inherit Metab Dis; 1989; 12 Suppl 1():231-46. PubMed ID: 2681997
[TBL] [Abstract][Full Text] [Related]
9. A deletion panel of the long arm of the X chromosome: subregional localization of 22 DNA probes.
Yang HM; Lund T; Niebuhr E; Nørby S; Schwartz M; Shen L
Hum Genet; 1990 Jun; 85(1):25-30. PubMed ID: 1972695
[TBL] [Abstract][Full Text] [Related]
10. Medical genetics.
Super M
Postgrad Med J; 1991 Jul; 67(789):613-31. PubMed ID: 1924046
[No Abstract] [Full Text] [Related]
11. Bibliography on X-linked mental retardation, the fragile X and related subjects IV (1988).
Spano LM; Opitz JM
Am J Med Genet; 1988; 30(1-2):31-60. PubMed ID: 3052063
[No Abstract] [Full Text] [Related]
12. 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]
13. Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers.
Oberlé I; Heilig R; Moisan JP; Kloepfer C; Mattéi GM; Mattéi JF; Boué J; Froster-Iskenius U; Jacobs PA; Lathrop GM
Proc Natl Acad Sci U S A; 1986 Feb; 83(4):1016-20. PubMed ID: 3006023
[TBL] [Abstract][Full Text] [Related]
14. Molecular genetics of the human X chromosome.
Davies KE
J Med Genet; 1985 Aug; 22(4):243-9. PubMed ID: 2995673
[TBL] [Abstract][Full Text] [Related]
15. Linkage analysis of X-linked mental retardation with and without fragile-X using factor IX gene probe.
Choo KH; George D; Filby G; Halliday JL; Leversha M; Webb G; Danks DM
Lancet; 1984 Aug; 2(8398):349. PubMed ID: 6146889
[No Abstract] [Full Text] [Related]
16. Fragile X syndrome: a major cause of X-linked mental retardation.
Butler MG
Compr Ther; 1988 Jul; 14(7):3-7. PubMed ID: 3060303
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
