39 related articles for article (PubMed ID: 1552536)
21. Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1).
Hallam PJ; Harding AE; Berciano J; Barker DF; Malcolm S
Ann Neurol; 1992 May; 31(5):570-2. PubMed ID: 1596093
[TBL] [Abstract][Full Text] [Related]
22. Charcot-Marie-Tooth neuropathy type 1A mutation: apparent crossovers with D17S122 are due to a duplication.
Nicholson GA; Kennerson ML; Keats BJ; Mesterovic N; Churcher W; Barker D; Ross DA
Am J Med Genet; 1992 Nov; 44(4):455-60. PubMed ID: 1442887
[TBL] [Abstract][Full Text] [Related]
23. Evidence for linkage of Charcot-Marie-Tooth neuropathy to the Duffy locus on chromosome 1.
Bird TD; Ott J; Giblett ER
Am J Hum Genet; 1982 May; 34(3):388-94. PubMed ID: 6952764
[TBL] [Abstract][Full Text] [Related]
24. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.
Feinberg AP; Vogelstein B
Anal Biochem; 1983 Jul; 132(1):6-13. PubMed ID: 6312838
[TBL] [Abstract][Full Text] [Related]
25. Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17.
Vance JM; Nicholson GA; Yamaoka LH; Stajich J; Stewart CS; Speer MC; Hung WY; Roses AD; Barker D; Pericak-Vance MA
Exp Neurol; 1989 May; 104(2):186-9. PubMed ID: 2707366
[TBL] [Abstract][Full Text] [Related]
26. Hereditary motor-sensory neuropathies. Charcot-Marie-Tooth syndrome.
Bird TD
Neurol Clin; 1989 Feb; 7(1):9-23. PubMed ID: 2646524
[TBL] [Abstract][Full Text] [Related]
27. A genetic map of human chromosome 17p.
Wright EC; Goldgar DE; Fain PR; Barker DF; Skolnick MH
Genomics; 1990 May; 7(1):103-9. PubMed ID: 2335351
[TBL] [Abstract][Full Text] [Related]
28. Hereditary motor and sensory neuropathies.
Vance JM
J Med Genet; 1991 Jan; 28(1):1-5. PubMed ID: 1999826
[No Abstract] [Full Text] [Related]
29. Single-gene neurological disorders in South Wales: an epidemiological study.
MacMillan JC; Harper PS
Ann Neurol; 1991 Sep; 30(3):411-4. PubMed ID: 1952829
[TBL] [Abstract][Full Text] [Related]
30. Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a). The HMSN Collaborative Research Group.
Raeymaekers P; Timmerman V; Nelis E; De Jonghe P; Hoogendijk JE; Baas F; Barker DF; Martin JJ; De Visser M; Bolhuis PA
Neuromuscul Disord; 1991; 1(2):93-7. PubMed ID: 1822787
[TBL] [Abstract][Full Text] [Related]
31. Charcot-Marie-Tooth disease type 1a (CMT1a): evidence for trisomy of the region p11.2 of chromosome 17 in south Wales families.
MacMillan JC; Upadhyaya M; Harper PS
J Med Genet; 1992 Jan; 29(1):12-3. PubMed ID: 1552536
[TBL] [Abstract][Full Text] [Related]
32. Charcot-Marie-Tooth disease type 1A: molecular mechanisms of gene dosage and point mutation underlying a common inherited peripheral neuropathy.
Roa BB; Garcia CA; Lupski JR
Int J Neurol; 1991-1992; 25-26():97-107. PubMed ID: 11980069
[TBL] [Abstract][Full Text] [Related]
33. Correlation between the histopathologic, genotypic, and phenotypic features of hereditary peripheral neuropathies in childhood.
Ouvrier R
J Child Neurol; 1996 Mar; 11(2):133-46. PubMed ID: 8881991
[TBL] [Abstract][Full Text] [Related]
34. Charcot-Marie-Tooth disease type 1.
Malcolm S
J Med Genet; 1992 Jan; 29(1):3-4. PubMed ID: 1552540
[No Abstract] [Full Text] [Related]
35. DNA diagnostics for Charcot-Marie-Tooth disease and related inherited neuropathies.
Lupski JR
Clin Chem; 1996 Jul; 42(7):995-8. PubMed ID: 8674212
[No Abstract] [Full Text] [Related]
36.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
37.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
38.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
39.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Previous] [New Search]
