Bi-allelic variants in DNA mismatch repair proteins MutS Homolog MSH4 and MSH5 cause infertility in both sexes
Wyrwoll, M J, van Walree, E S, Hamer, G, Rotte, N, Motazacker, M M, Meijers-Heijboer, H, Alders, M, Meißner, A, Kaminsky, E, Wöste, M, Krallmann, C, Kliesch, S, Hunt, T J, Clark, A T, Silber, S, Stallmeyer, B, Friedrich, C, van Pelt, A M M, Mathijssen, I B, Tüttelmann, F
Published in Human reproduction (Oxford) (27.12.2021)
Published in Human reproduction (Oxford) (27.12.2021)
Get full text
Journal Article
Sequence analysis of 37 candidate genes for male infertility: challenges in variant assessment and validating genes
Araujo, T. F., Friedrich, C., Grangeiro, C. H. P., Martelli, L. R., Grzesiuk, J. D., Emich, J., Wyrwoll, M. J., Kliesch, S., Simões, A. L., Tüttelmann, F.
Published in Andrology (Oxford) (01.03.2020)
Published in Andrology (Oxford) (01.03.2020)
Get full text
Journal Article
Analysis of copy number variation in men with non‐obstructive azoospermia
Wyrwoll, M. J., Wabschke, R., Röpke, A., Wöste, M., Ruckert, C., Perrey, S., Rotte, N., Hardy, J., Astica, L., Lupiáñez, D. G., Wistuba, J., Westernströer, B., Schlatt, S., Berman, A. J., Müller, A. M., Kliesch, S., Yatsenko, A. N., Tüttelmann, F., Friedrich, C.
Published in Andrology (Oxford) (01.11.2022)
Published in Andrology (Oxford) (01.11.2022)
Get full text
Journal Article
Decreased spermatogonial numbers in boys with severe haematological diseases
Lahtinen, Atte K., Funke, Miriam, Krallmann, Claudia, Wyrwoll, Margot J., Jarisch, Andrea, Yang, Yifan, Bjarnason, Ragnar, Romerius, Patrik, Sundin, Mikael, Norén‐Nyström, Ulrika, Langenskiöld, Cecilia, Cremers, Jann‐Frederik, Kliesch, Sabine, Stukenborg, Jan‐Bernd, Neuhaus, Nina, Jahnukainen, Kirsi
Published in British journal of haematology (01.07.2024)
Published in British journal of haematology (01.07.2024)
Get full text
Journal Article