McKeown C - Search Results

1

Genomic imprinting in an Angelman and Prader-Willi translocation family.

Hultén M, Armstrong S, Challinor P, Gould C, Hardy G, Leedham P, Lee T, McKeown C. Hultén M, et al. Among authors: mckeown c. Lancet. 1991 Sep 7;338(8767):638-9. doi: 10.1016/0140-6736(91)90652-6. Lancet. 1991. PMID: 1679180 No abstract available.

2

Molecular cytogenetics of Prader-Willi and Angelman syndromes.

Hultén M, Hardy G, Gould C, Stergianou R, Waters J, McKeown C. Hultén M, et al. Among authors: mckeown c. Lancet. 1992 Jan 25;339(8787):243-4. doi: 10.1016/0140-6736(92)90043-3. Lancet. 1992. PMID: 1346195 No abstract available.

3

Rapid interphase FISH diagnosis of trisomy 18 on blood smears.

McKeown CM, Waters JJ, Stacey M, Newman BF, Cardy DL, Hultén M. McKeown CM, et al. Lancet. 1992 Aug 22;340(8817):495. doi: 10.1016/0140-6736(92)91823-q. Lancet. 1992. PMID: 1354828 No abstract available.

4

Germline APC mutation familial adenomatous polyposis in Indian family.

Wallis Y, MacDonald F, Rindl PM, Hulten M, McKeown C, Morton DG, Keighley MR, Fodde R, van der Luijt R, Khan PM. Wallis Y, et al. Among authors: mckeown c. Lancet. 1992 Oct 24;340(8826):1035. doi: 10.1016/0140-6736(92)93045-o. Lancet. 1992. PMID: 1357420 No abstract available.

5

Detection of an atypical 22q11 deletion that has no overlap with the DiGeorge syndrome critical region.

O'Donnell H, McKeown C, Gould C, Morrow B, Scambler P. O'Donnell H, et al. Among authors: mckeown c. Am J Hum Genet. 1997 Jun;60(6):1544-8. doi: 10.1016/S0002-9297(07)64250-5. Am J Hum Genet. 1997. PMID: 9199579 Free PMC article. No abstract available.

6

Southern analysis reveals a large deletion at the hypoxanthine phosphoribosyltransferase locus in a patient with Lesch-Nyhan syndrome.

Renwick PJ, Birley AJ, McKeown CM, Hultén M. Renwick PJ, et al. Among authors: mckeown cm. Clin Genet. 1995 Aug;48(2):80-4. doi: 10.1111/j.1399-0004.1995.tb04060.x. Clin Genet. 1995. PMID: 7586656

7

Exclusion of an elastin gene (ELN) mutation as the cause of pseudoxanthoma elasticum (PXE) in one family.

Raybould MC, Birley AJ, Moss C, Hultén M, McKeown CM. Raybould MC, et al. Among authors: mckeown cm. Clin Genet. 1994 Jan;45(1):48-51. doi: 10.1111/j.1399-0004.1994.tb03990.x. Clin Genet. 1994. PMID: 8149653

8

Mosaic trisomy 1q: The longest surviving case.

Patel C, Hardy G, Cox P, Bowdin S, McKeown C, Russell AB. Patel C, et al. Among authors: mckeown c. Am J Med Genet A. 2009 Aug;149A(8):1795-800. doi: 10.1002/ajmg.a.32959. Am J Med Genet A. 2009. PMID: 19610079

9

Predictive diagnosis of familial adenomatous polyposis with linked DNA markers: population based study.

MacDonald F, Morton DG, Rindl PM, Haydon J, Cullen R, Gibson J, Neoptolemos JP, Keighley MR, McKeown CM, Hultén M. MacDonald F, et al. Among authors: mckeown cm. BMJ. 1992 Apr 4;304(6831):869-72. doi: 10.1136/bmj.304.6831.869. BMJ. 1992. PMID: 1327364 Free PMC article.

10

Genotype-phenotype correlation between position of constitutional APC gene mutation and CHRPE expression in familial adenomatous polyposis.

Wallis YL, Macdonald F, Hultén M, Morton JE, McKeown CM, Neoptolemos JP, Keighley M, Morton DG. Wallis YL, et al. Among authors: mckeown cm. Hum Genet. 1994 Nov;94(5):543-8. doi: 10.1007/BF00211023. Hum Genet. 1994. PMID: 7959691

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