The spectrum of RB1 germ-line mutations in hereditary retinoblastoma von Lohmann, D R, Brandt, B, Höpping, W, Passarge, E, Horsthemke, B

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Dissecting Hirschsprung disease von Passarge, Eberhard

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A distinctive phenotype associated with an interstitial deletion 6q14 contained within a de novo pericentric inversion 6 (p11.2q15) von Passarge, E.

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Incorrect use of the term synteny von Passarge, Eberhard, Horsthemke, Bernhard, Farber, Rosann A

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German job security leads to stagnation von Passarge, Eberhard

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Professor Herbert Theile, Leipzig, zum Geburtstag von Passarge, E.

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Uniparental isodisomy for paternal 2p and maternal 2q in a phenotypically normal female with two isochromosomes, i(2p) and i(2q) von ALBRECHT, BEATE, MERGENTHALER, SUSANNE, EGGERMANN, KATJA, ZERRES, KLAUS, PASSARGE, EBERHARD, EGGERMANN, THOMAS

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Corrigendum: Transcriptional regulator PRDM12 is essential for human pain perception von Chen, Ya-Chun, Auer-Grumbach, Michaela, Matsukawa, Shinya, Zitzelsberger, Manuela, Themistocleous, Andreas C, Strom, Tim M, Samara, Chrysanthi, Moore, Adrian W, Cho, Lily Ting-Yin, Young, Gareth T, Weiss, Caecilia, Schabhüttl, Maria, Stucka, Rolf, Schmid, Annina B, Parman, Yesim, Graul-Neumann, Luitgard, Heinritz, Wolfram, Passarge, Eberhard, Watson, Rosemarie M, Hertz, Jens Michael, Moog, Ute, Baumgartner, Manuela, Valente, Enza Maria, Pereira, Diego, Restrepo, Carlos M, Katona, Istvan, Dusl, Marina, Stendel, Claudia, Wieland, Thomas, Stafford, Fay, Reimann, Frank, von Au, Katja, Finke, Christian, Willems, Patrick J, Nahorski, Michael S, Shaikh, Samiha S, Carvalho, Ofélia P, Nicholas, Adeline K, Karbani, Gulshan, McAleer, Maeve A, Cilio, Maria Roberta, McHugh, John C, Murphy, Sinead M, Irvine, Alan D, Jensen, Uffe Birk, Windhager, Reinhard, Weis, Joachim, Bergmann, Carsten, Rautenstrauss, Bernd, Baets, Jonathan, De Jonghe, Peter, Reilly, Mary M, Kropatsch, Regina, Kurth, Ingo, Chrast, Roman, Michiue, Tatsuo, Bennett, David L H, Woods, C Geoffrey, Senderek, Jan

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Professor Herbert Theile, Leipzig, zum Geburtstag von Passarge, E.

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Holger Höhn, Professor emeritus (aktiv) von Passarge, E., Ropers, H.H.

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Constitutional RB1-Gene Mutations in Patients with Isolated Unilateral Retinoblastoma von Lohmann, Dietmar R., Gerick, Martin, Brandt, Birgit, Oelschläger, Ulrich, Lorenz, Birgit, Passarge, Eberhard, Horsthemke, Bernhard

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Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens von DÖRK, T, DWORNICZAK, B, PANDER, H.-J, SPERLING, H, RATJEN, F, PASSARGE, E, SCHMIDTKE, J, STUHRMANN, M, AULEHLA-SCHOLZ, C, WIECZOREK, D, BÖHM, I, MAYEROVA, A, SEYDEWITZ, H. H, NIESCHLAG, E, MESCHEDE, D, HORST, J

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Emil Heitz and the concept of heterochromatin: longitudinal chromosome differentiation was recognized fifty years ago von Passarge, E

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Prenatal diagnosis and management of congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency von Passarge, E

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A SIMPLE AND NONRADIOACTIVE METHOD FOR DETECTING THE RB1.20 DNA POLYMORPHISM IN THE RETINOBLASTOMA GENE von BRANDT, B, GREGER, YANDELL, D, PASSARGE, E, HORSTHEMKE, B

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Wither polygenic inheritance: Mapping Hirschsprung disease von Passarge, Eberhard

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Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastoma von GREGER, V, PASSARGE, E, HÖPPING, W, MESSMER, E, HORSTHEMKE, B

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An excess of chromosome 1 breakpoints in male infertility von BACHE, Ihen, VAN ASSCHE, Elvire, KALSCHEUER, Vera, LIEBAERS, Inge, BONDUELLE, Maryse, TOURNAYE, Herman, AYUSO, Carmen, BARBI, Gotthold, BLENNOW, Elisabeth, BOURROUILLOU, Georges, BRONDUM-NIELSEN, Karen, BRUUN-PETERSEN, Gert, CINGOZ, Sultan, CROQUETTE, Marie-Francoise, DAHOUN, Sophie, DALLAPICCOLA, Bruno, DAVISON, Val, DELOBEL, Bruno, DUBA, Hans-Christoph, DUPREZ, Laurence, FERGUSON-SMITH, Malcolm, FITZPATRICK, David R, GRACE, Elizabeth, BUGGE, Merete, HANSMANN, Ingo, HULTEN, Maj, JENSEN, Peter Ka, JONVEAUX, Philippe, KRISTOFFERSSON, Ulf, LOPEZ-PAJARES, Isidora, MCGOWAN-JORDAN, Jean, MURKEN, Jan, ORERA, Maria, PARKIN, Tony, TÜMER, Zeynep, PASSARGE, Eberhard, RAMOS, Carmen, RASMUSSEN, Kirsten, SCHEMPP, Werner, SCHUBERT, Regine, SCHWINGER, Eberhard, SHABTAI, Fiorella, SMITH, Kim, STALLINGS, Raymond, STEFANOVA, Margarita, HJORTH, Mads, TRANEBJERG, Lisbeth, TURLEAU, Catherine, BIRGER VAN DER HAGEN, Carl, VEKEMANS, Michel, KOKALJ VOKAC, Nadja, WAGNER, Klaus, WAHLSTROEM, Jan, ZELANTE, Leopoldo, TOMMERUP, Niels, LUNDSTEEN, Claes, LESPINASSE, James, WINTHER, Kirsten, NIEBUHR, Anita

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A DNA helicase in full Bloom von Passarge, Eberhard

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Frequency and parental origin of hypermethylated RB1 alleles in retinoblastoma von Greger, V, Debus, N, Lohmann, D, Höpping, W, Passarge, E, Horsthemke, B

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