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Genetic Epidemiology|November 30, 2011
On the analysis of sequence data: testing for disease susceptibility loci using patterns of linkage disequilibriumPeter J Lipman, Wai-Ki Yip, Taofik AlChawa, et al.
Frontiers in Cell and Developmental Biology|May 11, 2023
Analysis of candidate genes for cleft lip ± cleft palate using murine single-cell expression dataAnna Siewert, Benedikt Reiz, Carina Krug, et al.
European Journal of Human Genetics : EJHG|May 5, 2005
Hereditary nonpolyposis colorectal cancer: pitfalls in deletion screening in MSH2 and MLH1 genesMaria Wehner, Elisabeth Mangold, Marlies Sengteller, et al.
International Journal of Cancer|December 21, 2002
Hereditary nonpolyposis colorectal cancer: frequent occurrence of large genomic deletions in MSH2 and MLH1 genesYaping Wang, Waltraut Friedl, Christof Lamberti, et al.
The American Journal of Surgical Pathology|February 23, 2002
Loss of DNA mismatch repair proteins in skin tumors from patients with Muir-Torre syndrome and MSH2 or MLH1 germline mutations: establishment of immunohistochemical analysis as a screening testMicaela Mathiak, Arno Rütten, Elisabeth Mangold, et al.
Development (Cambridge, England)|May 30, 2020
Msx1 deficiency interacts with hypoxia and induces a morphogenetic regulation during mouse lip developmentMitsushiro Nakatomi, Kerstin U Ludwig, Michael Knapp, et al.
Neuropediatrics|July 19, 2019
Cleft Palate as Distinguishing Feature in a Patient with GABRB3 Epileptic EncephalopathyDaniel Bamborschke, Matthias Pergande, Hülya Sevcan Daimagüler, et al.
The Journal of Investigative Dermatology|April 26, 2003
Frequency of microsatellite instability in unselected sebaceous gland neoplasias and hyperplasiasRoland Kruse, Arno Rütten, Nadine Schweiger, et al.
International Journal of Cancer|September 2, 2003
Stromal expression of invasion-promoting, matrix-degrading proteases MMP-1 and -9 and the Ets 1 transcription factor in HNPCC carcinomas and sporadic colorectal cancersPeter Behrens, Micaela Mathiak, Elisabeth Mangold, et al.
Frontiers in Molecular Biosciences|September 12, 2022
Using CRISPR/Cas9 genome editing in human iPSCs for deciphering the pathogenicity of a novel CCM1 transcription start site deletionRobin A Pilz, Dariush Skowronek, Motaz Hamed, et al.
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