The mosaic hedgehog spectrum: another lesson on the polymorphy of mosaicism von Zenker, M.

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Assessing insect biodiversity with automatic light traps in Brazil: Pearls and pitfalls of metabarcoding samples in preservative ethanol von Zenker, Mauricio M., Specht, Alexandre, Fonseca, Vera G.

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Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromes von Kratz, C P, Franke, L, Peters, H, Kohlschmidt, N, Kazmierczak, B, Finckh, U, Bier, A, Eichhorn, B, Blank, C, Kraus, C, Kohlhase, J, Pauli, S, Wildhardt, G, Kutsche, K, Auber, B, Christmann, A, Bachmann, N, Mitter, D, Cremer, F W, Mayer, K, Daumer-Haas, C, Nevinny-Stickel-Hinzpeter, C, Oeffner, F, Schlüter, G, Gencik, M, Überlacker, B, Lissewski, C, Schanze, I, Greene, M H, Spix, C, Zenker, M

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Argon plasma coagulation for open surgical and endoscopic applications: state of the art von Raiser, J, Zenker, M

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MRI Spectrum of Brain Involvement in Sphingosine-1-Phosphate Lyase Insufficiency Syndrome von Martin, K. W., Weaver, N., Alhasan, K., Gumus, E., Sullivan, B. R., Zenker, M., Hildebrandt, F., Saba, J. D.

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Michel Pierson's syndrome von Cochat, P, Zenker, M

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Facets of shame are differently expressed in dermatological disease: a prospective observational study von Aberer, E., Hiebler‐Ragger, M., Zenker, M., Weger, W., Hofer, A., Unterrainer, H.F.

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Fast Census of Moth Diversity in the Neotropics: A Comparison of Field-Assigned Morphospecies and DNA Barcoding in Tiger Moths von Zenker, Mauricio M, Rougerie, Rodolphe, Teston, José A, Laguerre, Michel, Pie, Marcio R, Freitas, André V L

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Reducing the incidence of acute puerperal metritis in primiparous cows by application of pegbovigrastim in a Holstein dairy herd von Freick, M., Zenker, M., Passarge, O., Weber, J.

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Timeline and geographical distribution of Helicoverpa armigera (Hübner) (Lepidoptera, Noctuidae: Heliothinae) in Brazil von Sosa-Gómez, Daniel R., Specht, Alexandre, Paula-Moraes, Silvana V., Lopes-Lima, Adilson, Yano, Silvia A.C., Micheli, Adriana, Morais, Elisangela G.F., Gallo, Paulo, Pereira, Paulo R.V.S., Salvadori, José R., Botton, Marcos, Zenker, Maurício M., Azevedo-Filho, Wilson S.

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Systematized naevoid hypertrichosis may herald Happle–Tinschert syndrome von Hasbún, T., Reculé, F., Happle, R., Zenker, M., Schanze, D., Castro, A.

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Application of ultrasound-assisted thermal processing for preservation and quality retention of liquid foods von Zenker, M, Heinz, V, Knorr, D

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Specific mosaic KRAS mutations affecting codon 146 cause oculoectodermal syndrome and encephalocraniocutaneous lipomatosis von Boppudi, S., Bögershausen, N., Hove, H.B., Percin, E.F., Aslan, D., Dvorsky, R., Kayhan, G., Li, Y., Cursiefen, C., Tantcheva-Poor, I., Toft, P.B., Bartsch, O., Lissewski, C., Wieland, I., Jakubiczka, S., Wollnik, B., Ahmadian, M.R., Heindl, L.M., Zenker, M.

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Tiger-Moths in Savannas in Eastern Amazon: First Assessment of Diversity and Seasonal Aspects von Valente, D M P, Zenker, M M, Teston, J A

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Electrical and rheological characterization of poly(trimethylene terephthalate) hybrid nanocomposites filled with COOH functionalized MWCNT and graphene nanosheets von Paszkiewicz, S., Szymczyk, A., Kasprowiak, I., Zenker, M., Pilawka, R., Linares, A., Ezquerra, T. A., Rosłaniec, Z.

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Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS) von Gbadegesin, Rasheed, Hinkes, Bernward G., Hoskins, Bethan E., Vlangos, Christopher N., Heeringa, Saskia F., Liu, Jinhong, Loirat, Chantal, Ozaltin, Fatih, Hashmi, Seema, Ulmer, Francis, Cleper, Roxanna, Ettenger, Robert, Antignac, Corinne, Wiggins, Roger C., Zenker, Martin, Hildebrandt, Friedhelm

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Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders von Hasselbacher, K., Wiggins, R.C., Matejas, V., Hinkes, B.G., Mucha, B., Hoskins, B.E., Ozaltin, F., Nürnberg, G., Becker, C., Hangan, D., Pohl, M., Kuwertz-Bröking, E., Griebel, M., Schumacher, V., Royer-Pokora, B., Bakkaloglu, A., Nürnberg, P., Zenker, M., Hildebrandt, F.

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Functional analysis of a duplication (p.E63_D69dup) in the switch II region of HRAS: new aspects of the molecular pathogenesis underlying Costello syndrome von Lorenz, Sybille, Lissewski, Christina, Simsek-Kiper, Pelin O, Alanay, Yasemin, Boduroglu, Koray, Zenker, Martin, Rosenberger, Georg

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Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1 von Slavotinek, Anne M, Baranzini, Sergio E, Schanze, Denny, Labelle-Dumais, Cassandre, Short, Kieran M, Chao, Ryan, Yahyavi, Mani, Bijlsma, Emilia K, Chu, Catherine, Musone, Stacey, Wheatley, Ashleigh, Kwok, Pui-Yan, Marles, Sandra, Fryns, Jean-Pierre, Maga, A Murat, Hassan, Mohamed G, Gould, Douglas B, Madireddy, Lohith, Li, Chumei, Cox, Timothy C, Smyth, Ian, Chudley, Albert E, Zenker, Martin

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Two novel germline KRAS mutations: expanding the molecular and clinical phenotype von Stark, Z, Gillessen-Kaesbach, G, Ryan, MM, Cirstea, IC, Gremer, L, Ahmadian, MR, Savarirayan, R, Zenker, M

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