Zobrazeno 1 - 10
of 70
pro vyhledávání: '"M. Döbler"'
Autor:
I. Krägeloh-Mann, M. Moll, R. Gölz, M. Schöning, M. Döbler-Neumann, Christian F. Poets, J. Arand
Publikováno v:
Klinische Pädiatrie. 223:251-254
BACKGROUND Since 2008, follow-up examinations at 2 years of age with the standardized Bayley II test have become obligatory in Germany for all very low birth weight infants. AIM We already performed such examinations before 2006. Here, we compared ou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::378eedca8519ff92e4b105340582c3ce
https://doi.org/10.1055/s-0031-1275679
https://doi.org/10.1055/s-0031-1275679
Autor:
Manfred Schartl, Roman Fuchs, Jakob Parzefall, M. Döbler, Dunja K. Lamatsch, Robin Wacker, Ingo Schlupp, Matthias Stöck
Publikováno v:
Journal of Fish Biology, vol. 77, no. 7, pp. 1459-1487
In a microchromosome-carrying laboratory stock of the normally all-female Amazon molly Poecilia formosa triploid individuals were obtained, all of which spontaneously developed into males. A comparison of morphology of the external and internal insem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62a2f1a200230b73b22f04b6be5b3a84
https://doi.org/10.1111/j.1095-8649.2010.02766.x
https://doi.org/10.1111/j.1095-8649.2010.02766.x
Autor:
T Höller, M Debald, M Keyver-Paik, A Abramian, M Döbler, Martin Braun, C. Kuhl, C Leutner, W Kuhn, L Nemes, H Schild, C Kaiser
Publikováno v:
Senologie - Zeitschrift für Mammadiagnostik und -therapie. 12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75779ef242913954cd7d3883b63ee3b1
https://doi.org/10.1055/s-0035-1550458
https://doi.org/10.1055/s-0035-1550458
Akademický článek
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Autor:
Manfred Schartl, Indrajit Nanda, J. Parzefall, Jörg T. Epplen, Dunja K. Lamatsch, Ingo Schlupp, M. Döbler, Michael Schmid
Publikováno v:
Cytogenetic and Genome Research. 80:193-198
All-female vertebrates are excellent model systems for studying many evolutionary problems. One of these is the Amazon molly. In this review, three aspects of its biology are discussed: (1) An important question is how dispensable genes, such as all
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33c27903dd9184813375e1ee8efb5701
https://doi.org/10.1159/000014979
https://doi.org/10.1159/000014979
Autor:
D. Meschede, W. Schempp, W. Traut, J. Klein, T.W. Glover, S.J. Palmer, J.T. Epplen, E.J.M. Santos, B.R. Migeon, R. Toder, J. Horst, M. Guttenbach, G. Bonnet, T. Matsunaga, C.V. Beechey, B. Choudhary, M. Cohn, D. Weichenhan, S. Ball, G. Bernardi, S. Lautsch, H. Winking, T. Vogel, E.Y. Cheng, K. Benirschke, N. Nassar, U. Wolf, J. Schmidtke, L.-S. Correa-Cerro, M. Sugimoto, W. Beçak, B. Kerem, T. Sharma, S.S. Wachtel, J. Zhang, A.T. Midro, K. Sperling, C. O’hUigin, V.V. Kapitonov, R. Lesniewicz, S.K. Mahadevaiah, W.R. Harrison, C. Geerkens, C. Dixkens, W. Just, H. Shibata, R.M. Cabrera, C.M. Disteche, M. Schartl, N. Zhdanova, J.A.M. Graves, U. Drews, S. Saccone, G.P. Holmquist, D.K. Lamatsch, M.F. Lyon, S. Zeitler, S.K. Davis, K. Bender, C. Klett, J. Bruch, G.G. Sharma, M.L. Houck, S. Henschel, N. Takagi, A.T. Kumamoto, R. Raman, H. Neitzel, P.S. Burgoyne, M. Erdel, O.L. Serov, A. Kollak, S. Jainta, S. Mizuno, Y. Hayashizaki, J. Jurka, F.A. Ponce de León, W. Rietschel, Y. Narain, B. Kunze, V. Kalscheuer, C. Ebenhoch, G. Beller, W. Rau, M. Held, A. Baumstark, J. Parzefall, T.J. Robinson, M. Digweed, S. Schmidt Drury, S.M. Gartler, M. Döbler, G. Wanner, Y.-F.C. Lau, H. Hameister, M.L. Beçak, H. Ogura, Y.-J. Chen, S. Takada, F.F.B. Elder, S. Ganesh, A. Ashworth, G. Scherer, K. Fredga, A. Sato, J. Perry, W. Vogel, I. Nanda, W. Mäueler, N. Mise, B.M. Cattanach, W. Feichtinger, H. Macgregor, R.P. Erickson, C. Federico, N.B. Atkin, S.-S. Tan, M. Schmid, I. Schlupp, K.M.S. Townsend, C. Steinlein
Publikováno v:
Cytogenetic and Genome Research. 80:12-15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2cb6077e25b3680f55832e9e23639ed
https://doi.org/10.1159/000014947
https://doi.org/10.1159/000014947
Autor:
C, Schroeder, A, Riess, M, Bonin, P, Bauer, O, Riess, M, Döbler-Neumann, S, Wieser, U, Moog, A, Tzschach
Publikováno v:
Clinical genetics. 86(3)
SHORT syndrome (OMIM 269880) is a rare autosomal-dominant disorder characterized by short stature, hyperextensibility of joints, hernias, ocular depression, ophthalmic anomalies (Rieger anomaly, posterior embryotoxon, glaucoma), teething delay, parti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::86a77a3be3911e32dbaf24f7899cd30b
https://pubmed.ncbi.nlm.nih.gov/23980586
https://pubmed.ncbi.nlm.nih.gov/23980586
Publikováno v:
Klinische Padiatrie. 223(4)
Since 2008, follow-up examinations at 2 years of age with the standardized Bayley II test have become obligatory in Germany for all very low birth weight infants.We already performed such examinations before 2006. Here, we compared our data and the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c464be77a880df08b79580e9d405e638
https://pubmed.ncbi.nlm.nih.gov/21563046
https://pubmed.ncbi.nlm.nih.gov/21563046
Publikováno v:
Neuropediatrics. 41
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ca904511a944deeefa7a98adf76981c
https://doi.org/10.1055/s-0030-1265592
https://doi.org/10.1055/s-0030-1265592
Akademický článek
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