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Year | Number of Results |
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1992 | 3 |
1997 | 1 |
2024 | 0 |
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Page 1
Fragile X syndrome is less common than previously estimated.
J Med Genet. 1997 Jan;34(1):1-5. doi: 10.1136/jmg.34.1.1.
J Med Genet. 1997.
PMID: 9032640
Free PMC article.
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: rindl pm.
Lancet. 1992 Oct 24;340(8826):1035. doi: 10.1016/0140-6736(92)93045-o.
Lancet. 1992.
PMID: 1357420
No abstract available.
Item in Clipboard
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: rindl pm.
BMJ. 1992 Apr 4;304(6831):869-72. doi: 10.1136/bmj.304.6831.869.
BMJ. 1992.
PMID: 1327364
Free PMC article.
Item in Clipboard
The use of DNA from paraffin wax preserved tissue for predictive diagnosis in familial adenomatous polyposis.
Morton DG, Macdonald F, Cachon-Gonzales MB, Rindl PM, Neoptolemos JP, Keighley MR, Delhanty JD, McKeown CM, Kilpatrick M, Hultén MA.
Morton DG, et al. Among authors: rindl pm.
J Med Genet. 1992 Aug;29(8):571-3. doi: 10.1136/jmg.29.8.571.
J Med Genet. 1992.
PMID: 1325558
Free PMC article.
No abstract available.
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