De novo stop‐lost germline mutation in FGFR3 causes severe chondrodysplasia in the progeny of a Holstein bull von Häfliger, I. M., Letko, A., Murgiano, L., Drögemüller, C.

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Prevalence of paunch calf syndrome carriers in Italian Romagnola cattle von Murgiano, L., Drögemüller, C., Sbarra, F., Bolcato, M., Gentile, A.

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Ellis–van Creveld Syndrome in Grey Alpine Cattle: Morphologic, Immunophenotypic, and Molecular Characterization von Muscatello, L. V., Benazzi, C., Dittmer, K. E., Thompson, K. G., Murgiano, L., Drögemüller, C., Avallone, G., Gentile, A., Edwards, J. F., Piffer, C., Bolcato, M., Brunetti, B.

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Frequency of bovine congenital pseudomyotonia carriers in selected Italian Chianina sires von Murgiano, L., Testoni, S., Drögemüller, C., Bolcato, M., Gentile, A.

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Redox proteomics: basic principles and future perspectives for the detection of protein oxidation in plants von Rinalducci, Sara, Murgiano, Leonardo, Zolla, Lello

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P6028 A frameshift mutation in MOCOS is associated with familial renal syndrome in Tyrolean Gray cattle von Murgiano, L., Jagannathan, V., Piffer, C., Drögemüller, C., Gentile, A.

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A frameshift mutation in MOCOS is associated with familial renal syndrome in Tyrolean Gray cattle von Murgiano, L, Jagannathan, V, Piffer, C, Drögemüller, C, Gentile, A

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Joint Formal Comment for PLGE and Commentary for G3 von Murgiano, Leonardo, Becker, Doreen, Torjman, Dina, Niggel, Jessica K., Milano, Ausra, Cullen, Cheryl, Feng, Rui, Wang, Fan, Jagannathan, Vidhya, Pearce-Kelling, Susan, Katz, Martin L., Leeb, Tosso, Aguirre, Gustavo D., Kaukonen, Maria, Quintero, Ileana B., Mukarram, Abdul K., Hytonen, Marjo K., Holopainen, Saila, Wickstrom, Kaisa, Kyostila, Kaisa, Arumilli, Meharji, Jalomaki, Sari, Daub, Carsten O., Kere, Juha, Lohi, Hannes

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P6015 An intronic MBTPS2 variant results in a splicing defect in horses with brindle coat texture von Murgiano, L., Waluk, D., Towers, R., Wiedemar, N., Dietrich, J., Jagannathan, V., Drögemüller, M., Druet, T., Galichet, A., Penedo, M. C., Müller, E., Roosje, P., Welle, M., Leeb, T.

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An intronic MBTPS2 variant results in a splicing defect in horses with brindle coat texture von Murgiano, L, Waluk, D, Towers, R, Wiedemar, N, Dietrich, J, Jagannathan, V, Drögemüller, M, Druet, T, Galichet, A, Penedo, M C, Müller, E, Roosje, P, Welle, M, Leeb, T

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Canine RNF170 Single Base Deletion in a Naturally Occurring Model for Human Neuroaxonal Dystrophy von Cook, Shawna R., Schwarz, Cleo, Guevar, Julien, Assenmacher, Charles‐Antoine, Sheehy, Maeve, Fanzone, Nathan, Church, Molly E., Murgiano, Leonardo, Casal, Margret L., Jagannathan, Vidhya, Gutierrez‐Quintana, Rodrigo, Lowrie, Mark, Steffen, Frank, Leeb, Tosso, Ekenstedt, Kari J.

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A naturally occurring canine model of syndromic congenital microphthalmia von Murgiano, Leonardo, Banjeree, Esha, O'Connor, Cynthia, Miyadera, Keiko, Werner, Petra, Niggel, Jessica K, Aguirre, Gustavo D, Casal, Margret L

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Complex Structural PPT1 Variant Associated with Non-syndromic Canine Retinal Degeneration von Murgiano, Leonardo, Becker, Doreen, Torjman, Dina, Niggel, Jessica K, Milano, Ausra, Cullen, Cheryl, Feng, Rui, Wang, Fan, Jagannathan, Vidhya, Pearce-Kelling, Sue, Katz, Martin L, Leeb, Tosso, Aguirre, Gustavo D

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Correction: Hairless Streaks in Cattle Implicate TSR2 in Early Hair Follicle Formation von Murgiano, Leonardo, Shirokova, Vera, Welle, Monika Maria, Jagannathan, Vidhya, Plattet, Philippe, Oevermann, Anna, Pienkowska-Schelling, Aldona, Gallo, Daniele, Gentile, Arcangelo, Mikkola, Marja L, Drögemüller, Cord

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Improving the resolution of canine genome‐wide association studies using genotype imputation: A study of two breeds von Jenkins, Christopher A., Schofield, Ellen C., Mellersh, Cathryn S., De Risio, Luisa, Ricketts, Sally L

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A putative silencer variant in a spontaneous canine model of retinitis pigmentosa von Kaukonen, Maria, Quintero, Ileana B., Mukarram, Abdul Kadir, Hytonen, Marjo K., Holopainen, Saila, Wickstrom, Kaisa, Kyostila, Kaisa, Arumilli, Meharji, Jalomaki, Sari, Daub, Carsten O., Kere, Juha, Lohi, Hannes

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RNF170 frameshift deletion in Miniature American Shepherd dogs with neuroaxonal dystrophy provides a naturally occurring model for human RNF170 phenotypic spectrum von Cook, Shawna R., Schwarz, Cleo, Guevar, Julien, Assenmacher, Charles-Antoine, Sheehy, Maeve, Fanzone, Nathan, Church, Molly E., Murgiano, Leonardo, Casal, Margret L., Jagannathan, Vidhya, Gutierrez-Quintana, Rodrigo, Lowrie, Mark, Steffen, Frank, Leeb, Tosso, Ekenstedt, Kari J.

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Hyperandrogenism and the fertility/sterility problem in couples with oligozoospermic patients von Frajese, G., Silveatroni, L., Falaschi, P., Mencacci-Amalfitano, M., Murgiano, S.

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Seminological, hormonal and histological evaluations of unilateral varicocele in relation to fertilizing potential von Frajese, G., Silvestroni, L., Mencacci-Amalfitano, M., Murgiano, S., Rocco, A., Magnani, A., De Giorgio, G., Di Silverio, F.

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