Abuse of genetics in Nazi Germany.

Por Propping, P
Publicado em 1992

Autosomal dominant polycystic kidney disease in children.

Por Zerres, K, Propping, P
Publicado em 1987

Schizophrenia: genetic tools for unraveling the nature of a complex disorder.

Por Propping, P, Nöthen, M M
Publicado em 1995

Hexosaminidase--pseudodeficiency?

Por Kappler, J, Gieselmann, V, Propping, P
Publicado em 1990

Association versus linkage studies in psychosis genetics.

Por Nöthen, M M, Propping, P, Fimmers, R
Publicado em 1993

Further RFLPs at the human tyrosine hydroxylase locus.

Por Körner, J, Uhlhaas, S, Mallet, J, Propping, P, Gal, A
Publicado em 1988

Severe persistent nasolacrimal duct obstruction: a typical finding in ADULT syndrome

Por Eter, N, Zerres, K, Propping, P, Roggenkämper, P, Spitznas, M
Publicado em 2006

Large Deletions in the BRCA1 Gene Are Not Common in a Set of Familial German Breast Cancer Patients

Por Maringa, M., Uhlhaas, S., Kreyer, E., Friedl, W., Propping, P., Schmutzler, R. K.
Publicado em 1999

Excess of homozygosity at the dopamine D3 receptor gene in schizophrenia not confirmed.

Por Nöthen, M M, Cichon, S, Propping, P, Fimmers, R, Schwab, S G, Wildenauer, D B
Publicado em 1993

Large submicroscopic genomic APC deletions are a common cause of typical familial adenomatous polyposis

Por Aretz, S, Stienen, D, Uhlhaas, S, Pagenstecher, C, Mangold, E, Caspari, R, Propping, P, Friedl, W
Publicado em 2005

Pseudoautosomal marker DXYS20 and manic depression.

Por Nöthen, M M, Cichon, S, Erdmann, J, Körner, J, Rietschel, M, Rappold, G A, Fritze, J, Propping, P
Publicado em 1993

A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome

Por Mangold, E, Pagenstecher, C, Leister, M, Mathiak, M, Rutten, A, Friedl, W, Propping, P, Ruzicka, T, Kruse, R
Publicado em 2004

Evidence for linkage of spelling disability to chromosome 15.

Por Schulte-Körne, G, Grimm, T, Nöthen, M M, Müller-Myhsok, B, Cichon, S, Vogt, I R, Propping, P, Remschmidt, H
Publicado em 1998

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 col...

Por Lamberti, C, Kruse, R, Ruelfs, C, Caspari, R, Wang, Y, Jungck, M, Mathiak, M, Malayeri, H, Friedl, W, Sauerbruch, T, Propping, P
Publicado em 1999

Compound heterozygosity for metachromatic leukodystrophy and arylsulfatase A pseudodeficiency alleles is not associated with progressive neurological disease

Por Penzien, J. M., Kappler, J., Herschkowitz, N., Schuknecht, B., Leinekugel, P., Propping, P., Tønnesen, T., Lou, H., Moser, H., Zierz, S., Conzelmann, E., Gieselmann, V.
Publicado em 1993

A gene for universal congenital alopecia maps to chromosome 8p21-22.

Por Nöthen, M M, Cichon, S, Vogt, I R, Hemmer, S, Kruse, R, Knapp, M, Höller, T, Faiyaz ul Haque, M, Haque, S, Propping, P, Ahmad, M, Rietschel, M
Publicado em 1998

Nonreplication of linkage disequilibrium between the dopamine D4 receptor locus and Tourette syndrome.

Por Hebebrand, J, Nöthen, M M, Ziegler, A, Klug, B, Neidt, H, Eggermann, K, Lehmkuhl, G, Poustka, F, Schmidt, M H, Propping, P, Remschmidt, H
Publicado em 1997

Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families

Por Friedl, W, Caspari, R, Sengteller, M, Uhlhaas, S, Lamberti, C, Jungck, M, Kadmon, M, Wolf, M, Fahnenstich, J, Gebert, J, Moslein, G, Mangold, E, Propping, P
Publicado em 2001

Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria.

Por Kruse, R, Rütten, A, Lamberti, C, Hosseiny-Malayeri, H R, Wang, Y, Ruelfs, C, Jungck, M, Mathiak, M, Ruzicka, T, Hartschuh, W, Bisceglia, M, Friedl, W, Propping, P
Publicado em 1998

High proportion of large genomic deletions and a genotype–phenotype update in 80 unrelated families with juvenile polyposis syndrome

Por Aretz, S, Stienen, D, Uhlhaas, S, Stolte, M, Entius, M M, Loff, S, Back, W, Kaufmann, A, Keller, K‐M, Blaas, S H, Siebert, R, Vogt, S, Spranger, S, Holinski‐Feder, E, Sunde, L, Propping, P, Friedl, W
Publicado em 2007