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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1966 1
1967 2
1968 1
1969 7
1970 4
1971 6
1972 5
1973 7
1974 6
1975 9
1977 5
1978 3
1979 4
1980 1
1981 2
1982 3
1983 3
1984 2
1985 3
1987 4
1988 4
1989 3
1990 4
1992 1
1993 3
1994 1
1996 7
1997 7
1998 4
1999 5
2000 6
2001 2
2002 3
2003 1
2004 3
2005 4
2006 5
2008 4
2011 1
2012 2
2013 2
2014 1
2016 1
2023 1
2024 1

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Search Results

151 results

Results by year

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Page 1
Partial trisomy 10p.
Grosse KP, Schwanitz G, Singer H, Wieczorek V. Grosse KP, et al. Among authors: schwanitz g. Humangenetik. 1975 Sep 10;29(2):141-4. doi: 10.1007/BF00430351. Humangenetik. 1975. PMID: 1176136
Analysis of acute COVID-19 including chronic morbidity: protocol for the deep phenotyping National Pandemic Cohort Network in Germany (NAPKON-HAP).
Steinbeis F, Thibeault C, Steinbrecher S, Ahlgrimm Y, Haack IA, August D, Balzuweit B, Bellinghausen C, Berger S, Chaplinskaya-Sobol I, Cornely O, Doeblin P, Endres M, Fink C, Finke C, Frank S, Hanß S, Hartung T, Hellmuth JC, Herold S, Heuschmann P, Heyckendorf J, Heyder R, Hippenstiel S, Hoffmann W, Kelle SU, Knape P, Koehler P, Kretzler L, Leistner DM, Lienau J, Lorbeer R, Lorenz-Depiereux B, Lüttke CD, Mai K, Merle U, Meyer-Arndt LA, Miljukov O, Muenchhoff M, Müller-Plathe M, Neuhann J, Neuhauser H, Nieters A, Otte C, Pape D, Pinto RM, Pley C, Pudszuhn A, Reuken P, Rieg S, Ritter P, Rohde G, Rönnefarth M, Ruzicka M, Schaller J, Schmidt A, Schmidt S, Schwachmeyer V, Schwanitz G, Seeger W, Stahl D, Stobäus N, Stubbe HC, Suttorp N, Temmesfeld B, Thun S, Triller P, Trinkmann F, Vadasz I, Valentin H, Vehreschild M, von Kalle C, von Lilienfeld-Toal M, Weber J, Welte T, Wildberg C, Wizimirski R, Zvork S, Sander LE, Vehreschild J, Zoller T, Kurth F, Witzenrath M. Steinbeis F, et al. Among authors: schwanitz g. Infection. 2024 Feb;52(1):93-104. doi: 10.1007/s15010-023-02057-0. Epub 2023 Jul 11. Infection. 2024. PMID: 37434025 Free PMC article.
[Microcephaly].
Neuhäuser G, Koch G, Schwanitz G. Neuhäuser G, et al. Among authors: schwanitz g. ZFA (Stuttgart). 1981 Jun 10;57(16):1211-8. ZFA (Stuttgart). 1981. PMID: 7257526 German. No abstract available.
[Progeria].
Koch G, Meyer-Robisch M, Schwanitz G. Koch G, et al. Among authors: schwanitz g. Folia Clin Int (Barc). 1966 Nov;16(11):528-30. Folia Clin Int (Barc). 1966. PMID: 5998574 Spanish. No abstract available.
[Mosaic Down's syndrome].
Grosse KP, Grosse G, Schwanitz G, Rott HD. Grosse KP, et al. Among authors: schwanitz g. Z Kinderheilkd. 1971;110(4):332-46. Z Kinderheilkd. 1971. PMID: 4254864 German. No abstract available.
Mosaic tetrasomy 14pterq13.1: longitudinal study.
Schwanitz G, Korsch E, Kremens-Korsch U, Ahlbory K, Gamerdinger U, Heidrich-Kaul C, Schubert R, Spengler S, Eggermann T. Schwanitz G, et al. Eur J Med Genet. 2011 Jul-Aug;54(4):e465-7. doi: 10.1016/j.ejmg.2011.03.003. Epub 2011 Mar 21. Eur J Med Genet. 2011. PMID: 21420515 No abstract available.
A phenotype map for 14q32.3 terminal deletions.
Engels H, Schüler HM, Zink AM, Wohlleber E, Brockschmidt A, Hoischen A, Drechsler M, Lee JA, Ludwig KU, Kubisch C, Schwanitz G, Weber RG, Leube B, Hennekam RC, Rudnik-Schöneborn S, Kreiss-Nachtsheim M, Reutter H. Engels H, et al. Among authors: schwanitz g. Am J Med Genet A. 2012 Apr;158A(4):695-706. doi: 10.1002/ajmg.a.35256. Epub 2012 Feb 24. Am J Med Genet A. 2012. PMID: 22367666
151 results