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HOLWELL FAMILY.
Published in:
Notes & Queries, 1924, v. CXLVI, n. mar15, p. 192-b
By:
- VON REUTTER, H. E.
Publication type:
Article
Mutations in CRLF1 cause familial achalasia.
Published in:
Clinical Genetics, 2017, v. 92, n. 1, p. 104, doi. 10.1111/cge.12953
By:
- Busch, A.;
- Žarković, M.;
- Lowe, C.;
- Jankofsky, M.;
- Ganschow, R.;
- Buers, I.;
- Kurth, I.;
- Reutter, H.;
- Rutsch, F.;
- Hübner, C.A.
Publication type:
Article
Comprehensive review of the duplication 3q syndrome and report of a patient with Currarino syndrome and de novo duplication 3q26.32-q27.2.
Published in:
Clinical Genetics, 2017, v. 91, n. 5, p. 661, doi. 10.1111/cge.12848
By:
- Dworschak, G.C.;
- Crétolle, C.;
- Hilger, A.;
- Engels, H.;
- Korsch, E.;
- Reutter, H.;
- Ludwig, M.
Publication type:
Article
Epispadias and the associated embryopathies: genetic and developmental basis.
Published in:
Clinical Genetics, 2017, v. 91, n. 2, p. 247, doi. 10.1111/cge.12871
By:
- Suzuki, K.;
- Matsumaru, D.;
- Matsushita, S.;
- Murashima, A.;
- Ludwig, M.;
- Reutter, H.;
- Yamada, G.
Publication type:
Article
The exstrophy-epispadias complex.
Published in:
2009
By:
- Ebert AK;
- Reutter H;
- Ludwig M;
- Rösch WH;
- Ebert, Anne-Karoline;
- Reutter, Heiko;
- Ludwig, Michael;
- Rösch, Wolfgang H
Publication type:
journal article
Strong Association of Variants around FOXE1 and Orofacial Clefting.
Published in:
Journal of Dental Research, 2014, v. 93, n. 4, p. 376, doi. 10.1177/0022034514523987
By:
- Ludwig, K.U.;
- Böhmer, A.C.;
- Rubini, M.;
- Mossey, P.A.;
- Herms, S.;
- Nowak, S.;
- Reutter, H.;
- Alblas, M.A.;
- Lippke, B.;
- Barth, S.;
- Paredes-Zenteno, M.;
- Muñoz-Jimenez, S.G.;
- Ortiz-Lopez, R.;
- Kreusch, T.;
- Hemprich, A.;
- Martini, M.;
- Braumann, B.;
- Jäger, A.;
- Pötzsch, B.;
- Molloy, A.
Publication type:
Article
Antimalarial and Antiarrhythmic Activity of Plant Extracts. 2. Acid Extracts of Plants.
Published in:
Pharmacology, 1969, v. 19, n. 2, p. 95, doi. 10.1159/000137184
By:
- Aviado, D.M.;
- Reutter, H.
Publication type:
Article
GENERAL AND VISCERAL SURGERY REVIEW.
Published in:
Journal of the Italian Surgical Association / Il Giornale di Chirurgia, 2012, v. 33, n. 6/7, p. 246
By:
- Schwarz, N. T.;
- Reutter, K-H.
Publication type:
Article
Human skim milk inhibits HTLV-1-cell-to-cell transmission.
Published in:
AIDS Reviews, 2023, v. 25, p. 24
By:
- A. K., Thoma-Kress;
- S., Heym;
- F., Wittdorf;
- N., Donhauser;
- P., Krebs;
- M., Kießling;
- P., Steininger;
- K., Korn;
- H., Reutter;
- A., Birzer
Publication type:
Article
Practice of dilatation after surgical correction in anorectal malformations.
Published in:
Pediatric Surgery International, 2012, v. 28, n. 11, p. 1095, doi. 10.1007/s00383-012-3169-4
By:
- Jenetzky, Ekkehart;
- Reckin, S.;
- Schmiedeke, E.;
- Schmidt, D.;
- Schwarzer, N.;
- Grasshoff-Derr, S.;
- Zwink, N.;
- Bartels, E.;
- Rißmann, A.;
- Leonhardt, J.;
- Weih, S.;
- Obermayr, F.;
- Rädecke, J.;
- Palta, M.;
- Kosch, F.;
- Götz, G.;
- Hofbauer, A.;
- Schäfer, M.;
- Reutter, H.;
- Holland-Cunz, S.
Publication type:
Article
Is specific antifungal therapy necessary for the treatment of guttural pouch mycosis in horses?
Published in:
Equine Veterinary Journal, 1995, v. 27, n. 2, p. 151, doi. 10.1111/j.2042-3306.1995.tb03053.x
By:
- SPEIRS, V. C.;
- HARRISON, I. W.;
- VEENENDAAL, J. C.;
- BAUMGARTNER, T.;
- JOSSECK, H. H.;
- REUTTER, H.
Publication type:
Article
Familial Translocation t(6;20)(p21;p13) Resulting in Partial Trisomy 6p and Partial Monosomy 20p: Report of a New Case and Review of the Literature.
Published in:
Cytogenetic & Genome Research, 2012, v. 136, n. 4, p. 308, doi. 10.1159/000337019
By:
- Berner, A.L.;
- Bağci, S.;
- Wohlleber, E.;
- Engels, E.;
- Müller, A.;
- Bartmann, P.;
- Weber, R.G.;
- Reutter, H.
Publication type:
Article
De novo Partial Trisomy 18p and Partial Monosomy 18q in a Patient with Anorectal Malformation.
Published in:
Cytogenetic & Genome Research, 2011, v. 134, n. 3, p. 243, doi. 10.1159/000328833
By:
- Bartels, E.;
- Draaken, M.;
- Kazmierczak, B.;
- Spranger, S.;
- Schramm, C.;
- Baudisch, F.;
- Nöthen, M.M.;
- Schmiedeke, E.;
- Ludwig, M.;
- Reutter, H.
Publication type:
Article
Genetische und molekularbiologische Aspekte des Blasenekstrophie-Epispadie-Komplexes (BEEK).
Published in:
Der Urologe A, 2005, v. 44, n. 9, p. 1037, doi. 10.1007/s00120-005-0863-z
By:
- Ludwig, M.;
- Utsch, B.;
- Reutter, H.
Publication type:
Article
Entwicklungsergebnis bei Blasenekstrophie und Epispadie aus Patientensicht Eine Pilotstudie.
Published in:
2005
By:
- Reutter, H;
- Lee, C;
- Grässer, M F;
- Noeker, M
Publication type:
journal article
Entwicklungsergebnis bei Blasenekstrophie und Epispadie aus Patientensicht.
Published in:
Der Urologe A, 2005, v. 44, n. 1, p. 57, doi. 10.1007/s00120-004-0739-7
By:
- Reutter, H.;
- Lee, C.;
- Gräßer, M.;
- Noeker, M.
Publication type:
Article
Microdeletions Including FMR1 in Three Female Patients with Intellectual Disability - Further Delineation of the Phenotype and Expression Studies.
Published in:
Molecular Syndromology, 2014, v. 5, n. 2, p. 65, doi. 10.1159/000357962
By:
- Zink, A.M.;
- Wohlleber, E.;
- Engels, H.;
- Rødningen, O.K.;
- Ravn, K.;
- Heilmann, S.;
- Rehnitz, J.;
- Katzorke, N.;
- Kraus, C.;
- Blichfeldt, S.;
- Hoffmann, P.;
- Reutter, H.;
- Brockschmidt, F.F.;
- Kreiß-Nachtsheim, M.;
- Vogt, P.H.;
- Prescott, T.E.;
- Tümer, Z.;
- Lee, J.A.
Publication type:
Article
VATER/VACTERL Association: Evidence for the Role of Genetic Factors.
Published in:
Molecular Syndromology, 2013, v. 4, n. 1/2, p. 16, doi. 10.1159/000345300
By:
- Reutter, H.;
- Ludwig, M.
Publication type:
Article

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