Malcolm S - Search Results

1

The phenotypic manifestations of chromosome 17p11.2 duplication.

Thomas PK, Marques W Jr, Davis MB, Sweeney MG, King RH, Bradley JL, Muddle JR, Tyson J, Malcolm S, Harding AE. Thomas PK, et al. Among authors: malcolm s. Brain. 1997 Mar;120 ( Pt 3):465-78. doi: 10.1093/brain/120.3.465. Brain. 1997. PMID: 9126058

2

Coexistence of hereditary motor and sensory neuropathy type Ia and IgM paraproteinemic neuropathy.

Gregory R, Thomas PK, King RH, Hallam PL, Malcolm S, Hughes RA, Harding AE. Gregory R, et al. Among authors: malcolm s. Ann Neurol. 1993 Jun;33(6):649-52. doi: 10.1002/ana.410330615. Ann Neurol. 1993. PMID: 8498845

3

Deletions of chromosome 17p11.2 in multifocal neuropathies.

Tyson J, Malcolm S, Thomas PK, Harding AE. Tyson J, et al. Among authors: malcolm s. Ann Neurol. 1996 Feb;39(2):180-6. doi: 10.1002/ana.410390207. Ann Neurol. 1996. PMID: 8967749

4

Hereditary demyelinating neuropathy of infancy. A genetically complex syndrome.

Tyson J, Ellis D, Fairbrother U, King RH, Muntoni F, Jacobs J, Malcolm S, Harding AE, Thomas PK. Tyson J, et al. Among authors: malcolm s. Brain. 1997 Jan;120 ( Pt 1):47-63. doi: 10.1093/brain/120.1.47. Brain. 1997. PMID: 9055797

5

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. Hallam PJ, et al. Among authors: malcolm s. Ann Neurol. 1992 May;31(5):570-2. doi: 10.1002/ana.410310518. Ann Neurol. 1992. PMID: 1596093

6

Linkage of hereditary motor and sensory neuropathy type I to the pericentromeric region of chromosome 17.

Middleton-Price HR, Harding AE, Monteiro C, Berciano J, Malcolm S. Middleton-Price HR, et al. Among authors: malcolm s. Am J Hum Genet. 1990 Jan;46(1):92-4. Am J Hum Genet. 1990. PMID: 2294757 Free PMC article.

7

Absence of linkage of hereditary motor and sensory neuropathy type I to chromosome 1 markers.

Middleton-Price HR, Harding AE, Berciano J, Pastor JM, Huson SM, Malcolm S. Middleton-Price HR, et al. Among authors: malcolm s. Genomics. 1989 Feb;4(2):192-7. doi: 10.1016/0888-7543(89)90299-1. Genomics. 1989. PMID: 2737679

8

No evidence for submicroscopic 22qter deletions in patients with features suggestive for Angelman syndrome.

de Vries BB, Tyson J, Winter RM, Malcolm S. de Vries BB, et al. Among authors: malcolm s. Am J Med Genet. 2002 Apr 22;109(2):117-20. doi: 10.1002/ajmg.10318. Am J Med Genet. 2002. PMID: 11977159

9

Mapping of DFN2 to Xq22.

Tyson J, Bellman S, Newton V, Simpson P, Malcolm S, Pembrey ME, Bitner-Glindzicz M. Tyson J, et al. Among authors: malcolm s. Hum Mol Genet. 1996 Dec;5(12):2055-60. doi: 10.1093/hmg/5.12.2055. Hum Mol Genet. 1996. PMID: 8968763

10

A boy with a submicroscopic 22qter deletion, general overgrowth and features suggestive of FG syndrome.

de Vries BB, Bitner-Glindzicz M, Knight SJ, Tyson J, MacDermont KD, Flint J, Malcolm S, Winter RM. de Vries BB, et al. Among authors: malcolm s. Clin Genet. 2000 Dec;58(6):483-7. doi: 10.1034/j.1399-0004.2000.580610.x. Clin Genet. 2000. PMID: 11149619

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