Author/Creator: Propping, P - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Propping, P

1. A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome. Issue 7 (2nd July 2004)

Authors:: Mangold, E; Pagenstecher, C; Leister, M; Mathiak, M; Rütten, A; Friedl, W; Propping, P; Ruzicka, T; Kruse, R
Journal:: Journal of medical genetics
Issue:: Volume 41:Issue 7(2004)
Page Start:: 567
Record Type:: Journal Article
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2. Association versus linkage studies in psychosis genetics. Issue 8 (August 1993)

Authors:: Nöthen, M M; Propping, P; Fimmers, R
Journal:: Journal of medical genetics
Issue:: Volume 30:Issue 8(1993)
Page Start:: 634
Record Type:: Journal Article
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3. Autosomal dominant polycystic kidney disease in children. Issue 8 (August 1987)

Authors:: Zerres, K; Propping, P
Journal:: Archives of disease in childhood
Issue:: Volume 62:Issue 8(1987)
Page Start:: 870
Record Type:: Journal Article
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4. Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families. Issue 4 (1st April 2001)

Authors:: Friedl, W; Caspari, R; Sengteller, M; Uhlhaas, S; Lamberti, C; Jungck, M; Kadmon, M; Wolf, M; Fahnenstich, J; Gebert, J; Möslein, G; Mangold, E; Propping, P
Journal:: Gut
Issue:: Volume 48:Issue 4(2001)
Page Start:: 515
Record Type:: Journal Article
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5. Excess of homozygosity at the dopamine D3 receptor gene in schizophrenia not confirmed. Issue 8 (August 1993)

Authors:: Nöthen, M M; Cichon, S; Propping, P; Fimmers, R; Schwab, S G; Wildenauer, D B
Journal:: Journal of medical genetics
Issue:: Volume 30:Issue 8(1993)
Page Start:: 708
Record Type:: Journal Article
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6. Large submicroscopic genomic APC deletions are a common cause of typical familial adenomatous polyposis. Issue 2 (2nd February 2005)

Authors:: Aretz, S; Stienen, D; Uhlhaas, S; Pagenstecher, C; Mangold, E; Caspari, R; Propping, P; Friedl, W
Journal:: Journal of medical genetics
Issue:: Volume 42:Issue 2(2005)
Page Start:: 185
Record Type:: Journal Article
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7. Microsatellite instability—a useful diagnostic tool to select patients at high risk for hereditary non-polyposis colorectal cancer: a study in different groups of patients with colorectal cancer. Issue 6 (1st June 1999)

Authors:: Lamberti, C; Kruse, R; Ruelfs, C; Caspari, R; Wang, Y; Jungck, M; Mathiak, M; Malayeri, H R H; Friedl, W; Sauerbruch, T; Propping, P
Journal:: Gut
Issue:: Volume 44:Issue 6(1999)
Page Start:: 839
Record Type:: Journal Article
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8. Severe persistent nasolacrimal duct obstruction: a typical finding in ADULT syndrome. Issue 9 (23rd August 2006)

Authors:: Eter, N; Zerres, K; Propping, P; Roggenkämper, P; Spitznas, M
Journal:: British journal of ophthalmology
Issue:: Volume 90:Issue 9(2006)
Page Start:: 1206
Record Type:: Journal Article
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9. Small bowel cancer risk in Lynch syndrome. Issue 11 (26th March 2008)

Authors:: Schulmann, K; Engel, C; Propping, P; Schmiegel, W
Journal:: Gut
Issue:: Volume 57:Issue 11(2008)
Page Start:: 1629
Record Type:: Journal Article
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