Nomenclature of esterases: another proposal.

von Wienker, T, von Deimling, O
Veröffentlicht 1987

On the genetics of mandibular prognathism: analysis of large European noble families.

von Wolff, G, Wienker, T F, Sander, H
Veröffentlicht 1993

A BAM HI RFLP at the human tyrosine aminotransferase (TAT) gene locus at 16q.

von Wullich, B, Natt, E, Wienker, T F, Scherer, G
Veröffentlicht 1989

Evidence for preferential X-chromosome inactivation in a family with Fabry disease.

von Ropers, H H, Wienker, T F, Grimm, T, Schroetter, K, Bender, K
Veröffentlicht 1977

Reply to Ogino and Wilson

von Feldkötter, Markus, Schwarzer, Verena, Wirth, Radu, Wienker, Thomas F., Wirth, Brunhilde
Veröffentlicht 2002

Quantitative Analyses of SMN1 and SMN2 Based on Real-Time LightCycler PCR: Fast and Highly Reliable Carrier Testing and Prediction of Severity of Spinal Muscular Atrophy

von Feldkötter, Markus, Schwarzer, Verena, Wirth, Radu, Wienker, Thomas F., Wirth, Brunhilde
Veröffentlicht 2002

Linkage studies in a pedigree with Van der Woude syndrome.

von Wienker, T F, Hudek, G, Bissbort, S, Mayerová, A, Mauff, G, Bender, K
Veröffentlicht 1987

Clinical reinvestigation and linkage analysis in the family with Episkopi blindness (Norrie disease).

von Wolff, G, Mayerová, A, Wienker, T F, Atalianis, P, Ioannou, P, Warburg, M
Veröffentlicht 1992

Evaluating information content of SNPs for sample-tagging in re-sequencing projects

von Hu, Hao, Liu, Xiang, Jin, Wenfei, Hilger Ropers, H, Wienker, Thomas F
Veröffentlicht in Sci Rep (2015)

Parametric and nonparametric multipoint linkage analysis with imprinting and two-locus-trait models: application to mite sensitization.

von Strauch, K, Fimmers, R, Kurz, T, Deichmann, K A, Wienker, T F, Baur, M P
Veröffentlicht 2000

Quantitative analysis of survival motor neuron copies: identification of subtle SMN1 mutations in patients with spinal muscular atrophy, genotype-phenotype correlation, and implica...

von Wirth, B, Herz, M, Wetter, A, Moskau, S, Hahnen, E, Rudnik-Schöneborn, S, Wienker, T, Zerres, K
Veröffentlicht 1999

The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene cluster.

von Vollmer, M, Jung, M, Rüschendorf, F, Ruf, R, Wienker, T, Reis, A, Krapf, R, Hildebrandt, F
Veröffentlicht 1998

Letters to the Editor

von Owen, M J, Williams, J, Mant, R, Asherson, P, McGuffin, P, Crocq, M-A, Wienker, T
Veröffentlicht 1993

Linkage analysis of alcohol dependence using MOD scores

von Strauch, Konstantin, Fürst, Robert, Rüschendorf, Franz, Windemuth, Christine, Dietter, Johannes, Flaquer, Antonia, Baur, Max P, Wienker, Thomas F
Veröffentlicht 2005

New mutation to Huntington's disease.

von Wolff, G, Deuschl, G, Wienker, T F, Hummel, K, Bender, K, Lücking, C H, Schumacher, M, Hammer, J, Oepen, G
Veröffentlicht 1989

Investigation of a Family with Autosomal Dominant Dilated Cardiomyopathy Defines a Novel Locus on Chromosome 2q14-q22

von Jung, Martin, Poepping, Imke, Perrot, Andreas, Ellmer, Annette E., Wienker, Thomas F., Dietz, Rainer, Reis, André, Osterziel, Karl Josef
Veröffentlicht 1999

Localization of the gene causing keratolytic winter erythema to chromosome 8p22-p23, and evidence for a founder effect in South African Afrikaans-speakers.

von Starfield, M, Hennies, H C, Jung, M, Jenkins, T, Wienker, T, Hull, P, Spurdle, A, Küster, W, Ramsay, M, Reis, A
Veröffentlicht 1997

Predictive value of Chartis measurement for lung function improvements in bronchoscopic lung volume reduction

von Wienker, Johannes, Karpf-Wissel, Rüdiger, Funke, Faustina, Taube, Christian, Wälscher, Julia, Winantea, Jane, Maier, Sandra, Mardanzai, Khaled, Darwiche, Kaid
Veröffentlicht in Ther Adv Respir Dis (2020)

Deletion at 12p in a Japanese child with brachydactyly overlaps the assigned locus of brachydactyly with hypertension in a Turkish family.

von Bähring, S, Nagai, T, Toka, H R, Nitz, I, Toka, O, Aydin, A, Mühl, A, Wienker, T F, Schuster, H, Luft, F C
Veröffentlicht 1997

Klüver–Bucy syndrome associated with a recessive variant in HGSNAT in two siblings with Mucopolysaccharidosis type IIIC (Sanfilippo C)

von Hu, Hao, Hübner, Christoph, Lukacs, Zoltan, Musante, Luciana, Gill, Esther, Wienker, Thomas F, Ropers, Hans-Hilger, Knierim, Ellen, Schuelke, Markus
Veröffentlicht in Eur J Hum Genet (2017)