Malcolm S - Search Results

1

Carrier detection for X-linked agammaglobulinaemia (Bruton type) in an Irish family using linked DNA probes.

Reardon W, Genet S, Middleton-Price H, Malcolm S, Feighery C. Reardon W, et al. Among authors: malcolm s. Ir Med J. 1991 Dec-1992 Jan;84(4):116-8. Ir Med J. 1991. PMID: 1817116

2

Clinical and genetic heterogeneity in X-linked deafness.

Reardon W, Middleton-Price HR, Malcolm S, Phelps P, Bellman S, Luxon L, Martin JA, Bumby A, Pembrey ME. Reardon W, et al. Among authors: malcolm s. Br J Audiol. 1992 Apr;26(2):109-14. doi: 10.3109/03005369209077878. Br J Audiol. 1992. PMID: 1628115

3

Mapping of the X linked form of hyper IgM syndrome (HIGM1).

Padayachee M, Levinsky RJ, Kinnon C, Finn A, McKeown C, Feighery C, Notarangelo LD, Hendriks RW, Read AP, Malcolm S. Padayachee M, et al. Among authors: malcolm s. J Med Genet. 1993 Mar;30(3):202-5. doi: 10.1136/jmg.30.3.202. J Med Genet. 1993. PMID: 8097258 Free PMC article.

4

Physical mapping identifies DXS265 as a useful genetic marker for carrier detection and prenatal diagnosis of X-linked agammaglobulinemia.

Lovering R, Sweatman AK, O'Reilly MA, Genet SA, Middleton-Price H, Malcolm S, Levinsky RJ, Kinnon C. Lovering R, et al. Among authors: malcolm s. Hum Genet. 1993 Mar;91(2):178-80. doi: 10.1007/BF00222721. Hum Genet. 1993. PMID: 8462977

5

Genetic and clinical heterogeneity of Stickler syndrome.

Vintiner GM, Temple IK, Middleton-Price HR, Baraitser M, Malcolm S. Vintiner GM, et al. Among authors: malcolm s. Am J Med Genet. 1991 Oct 1;41(1):44-8. doi: 10.1002/ajmg.1320410113. Am J Med Genet. 1991. PMID: 1683158

6

A multipedigree linkage study of X-linked deafness: linkage to Xq13-q21 and evidence for genetic heterogeneity.

Reardon W, Middleton-Price HR, Sandkuijl L, Phelps P, Bellman S, Luxon L, Pembrey ME, Malcolm S. Reardon W, et al. Among authors: malcolm s. Genomics. 1991 Dec;11(4):885-94. doi: 10.1016/0888-7543(91)90011-3. Genomics. 1991. PMID: 1783396

7

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.

8

Close linkage of PUM and SPTA within chromosome band 1q21.

Middleton-Price H, Gendler S, Malcolm S. Middleton-Price H, et al. Among authors: malcolm s. Ann Hum Genet. 1988 Oct;52(4):273-8. doi: 10.1111/j.1469-1809.1988.tb01107.x. Ann Hum Genet. 1988. PMID: 3268039

9

Close linkage of a gene for X linked deafness to three microsatellite repeats at Xq21 in radiologically normal and abnormal families.

Bitner-Glindzicz M, de Kok Y, Summers D, Huber I, Cremers FP, Ropers HH, Reardon W, Pembrey ME, Malcolm S. Bitner-Glindzicz M, et al. Among authors: malcolm s. J Med Genet. 1994 Dec;31(12):916-21. doi: 10.1136/jmg.31.12.916. J Med Genet. 1994. PMID: 7891371 Free PMC article.

10

Crouzon syndrome is not linked to craniosynostosis loci at 7p and 5qter.

Reardon W, van Herwerden L, Rose C, Jones B, Malcolm S, Winter RM. Reardon W, et al. Among authors: malcolm s. J Med Genet. 1994 Mar;31(3):219-21. doi: 10.1136/jmg.31.3.219. J Med Genet. 1994. PMID: 8014970 Free PMC article.

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