Wilson MJ - Search Results

1

Mowat DR, Wilson MJ, Goossens M. Mowat DR, et al. Among authors: wilson mj. J Med Genet. 2003 May;40(5):305-10. doi: 10.1136/jmg.40.5.305. J Med Genet. 2003. PMID: 12746390 Free PMC article. Review.

2

Distal 8p deletion (8p23.1----8pter): a common deletion?

Hutchinson R, Wilson M, Voullaire L. Hutchinson R, et al. J Med Genet. 1992 Jun;29(6):407-11. doi: 10.1136/jmg.29.6.407. J Med Genet. 1992. PMID: 1619636 Free PMC article.

3

New X-linked syndrome of mental retardation, gynecomastia, and obesity is linked to DXS255.

Wilson M, Mulley J, Gedeon A, Robinson H, Turner G. Wilson M, et al. Am J Med Genet. 1991 Sep 15;40(4):406-13. doi: 10.1002/ajmg.1320400405. Am J Med Genet. 1991. PMID: 1746601

4

Duplication of 5q11.2----q13.1 from a familial (5;20) balanced insertion.

Yip MY, Kemp J, Hanson N, Wilson M, Purvis-Smith S, Lam-Po-Tang PR. Yip MY, et al. Am J Med Genet. 1989 Jun;33(2):220-3. doi: 10.1002/ajmg.1320330215. Am J Med Genet. 1989. PMID: 2764031

5

Distinct skeletal abnormalities in four girls with Shprintzen-Goldberg syndrome.

Adès LC, Morris LL, Power RG, Wilson M, Haan EA, Bateman JF, Milewicz DM, Sillence DO. Adès LC, et al. Am J Med Genet. 1995 Jul 17;57(4):565-72. doi: 10.1002/ajmg.1320570410. Am J Med Genet. 1995. PMID: 7573130 Review.

6

X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome.

Gedeon AK, Wilson MJ, Colley AC, Sillence DO, Mulley JC. Gedeon AK, et al. Among authors: wilson mj. J Med Genet. 1995 May;32(5):383-8. doi: 10.1136/jmg.32.5.383. J Med Genet. 1995. PMID: 7616547 Free PMC article.

7

Desbuquois syndrome complicated by obstructive sleep apnoea and cervical kyphosis.

Ogle RF, Wilson MJ, Kozlowski K, Sillence DO. Ogle RF, et al. Among authors: wilson mj. Am J Med Genet. 1994 Jul 1;51(3):216-21. doi: 10.1002/ajmg.1320510308. Am J Med Genet. 1994. PMID: 8074147

8

Barth syndrome: clinical features and confirmation of gene localisation to distal Xq28.

Adès LC, Gedeon AK, Wilson MJ, Latham M, Partington MW, Mulley JC, Nelson J, Lui K, Sillence DO. Adès LC, et al. Among authors: wilson mj. Am J Med Genet. 1993 Feb 1;45(3):327-34. doi: 10.1002/ajmg.1320450309. Am J Med Genet. 1993. PMID: 8434619

9

Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23.

Mowat DR, Croaker GD, Cass DT, Kerr BA, Chaitow J, Adès LC, Chia NL, Wilson MJ. Mowat DR, et al. Among authors: wilson mj. J Med Genet. 1998 Aug;35(8):617-23. doi: 10.1136/jmg.35.8.617. J Med Genet. 1998. PMID: 9719364 Free PMC article.

10

Patient with a 22q11.2 deletion with no overlap of the minimal DiGeorge syndrome critical region (MDGCR).

McQuade L, Christodoulou J, Budarf M, Sachdev R, Wilson M, Emanuel B, Colley A. McQuade L, et al. Am J Med Genet. 1999 Sep 3;86(1):27-33. Am J Med Genet. 1999. PMID: 10440825

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