Works by Passarge, Eberhard

Results: 23

Lexikon der Syndrome und Fehlbildungen. Ursachen, Genetik, Risiken (2003): R. Witkowski, O. Prokop, E. Ullrich, G. Thiel: 7. Auflage, Springer-Verlag Berlin-Heidelberg-New York, ISBN 3-540-44305-3, hardcover, 1347 pages, 124.95 Euro.

Published in:

2004

By:

Passarge, Eberhard

Publication type:

Book Review

Hartwig Cleve.

Published in:

Clinical Genetics, 1995, v. 47, n. 2, p. 57, doi. 10.1111/j.1399-0004.1995.tb03924.x

By:

Bearn, Alexander G.;
Passarge, Eberhard

Publication type:

Article

Use of the RB1 cDNA as a diagnostic probe in retinoblastoma families.

Published in:

Clinical Genetics, 1990, v. 37, n. 2, p. 117, doi. 10.1111/j.1399-0004.1990.tb03488.x

By:

Goddard, Audrey D.;
Phillips, Robert A.;
Greger, Valerie;
Passarge, Eberhard;
Höpping, Wolfgang;
Zhu, Xiaoping;
Gallie, Brenda L.;
Horsthemke, Bernhard

Publication type:

Article

Bloom's Syndrome. XII. Report from the Registry for 1987.

Published in:

Clinical Genetics, 1989, v. 35, n. 1, p. 57, doi. 10.1111/j.1399-0004.1989.tb02905.x

By:

German, James;
Passarge, Eberhard

Publication type:

Article

Bloom's syndrome XI. Progress report for 1983.

Published in:

Clinical Genetics, 1984, v. 25, n. 2, p. 166, doi. 10.1111/j.1399-0004.1984.tb00480.x

By:

German, James;
Bloom, David;
Passarge, Eberhard

Publication type:

Article

Bloom's Syndrome. VII. Progress report for 1978.

Published in:

Clinical Genetics, 1979, v. 15, n. 4, p. 361, doi. 10.1111/j.1399-0004.1979.tb01747.x

By:

German, James;
Bloom, David;
Passarge, Eberhard

Publication type:

Article

Bloom's syndrome. V. Surveillance for cancer in affected families.

Published in:

Clinical Genetics, 1977, v. 12, n. 3, p. 162, doi. 10.1111/j.1399-0004.1977.tb00919.x

By:

German, James;
Bloom, David;
Passarge, Eberhard

Publication type:

Article

Dissecting Hirschsprung disease.

Published in:

Nature Genetics, 2002, v. 31, n. 1, p. 11, doi. 10.1038/ng878

By:

Passarge, Eberhard

Publication type:

Article

Incorrect use of the term synteny.

Published in:

Nature Genetics, 1999, v. 23, n. 4, p. 387, doi. 10.1038/70486

By:

Passarge, Eberhard;
Horsthemke, Bernhard;
Farber, Rosann A

Publication type:

Article

Improved prediction of complex diseases by common genetic markers: state of the art and further perspectives.

Published in:

Human Genetics, 2016, v. 135, n. 3, p. 259, doi. 10.1007/s00439-016-1636-z

By:

Müller, Bent;
Wilcke, Arndt;
Boulesteix, Anne-Laure;
Brauer, Jens;
Passarge, Eberhard;
Boltze, Johannes;
Kirsten, Holger

Publication type:

Article

Possible involvement of the retinoblastoma gene in undifferentiated sinonasal carcinoma.

Published in:

1990

By:

Greger, Valerie;
Schirmacher, Peter;
Bohl, Jürgen;
Bornemann, Antje;
Hürter, Thomas;
Passarge, Eberhard;
Horsthemke, Bernhard;
Greger, V;
Schirmacher, P;
Bohl, J;
Bornemann, A;
Hürter, T;
Passarge, E;
Horsthemke, B

Publication type:

journal article

Prenatally detected trisomy 4 and 6 mosaicism-cytogenetic results and clinical phenotype.

Published in:

Prenatal Diagnosis, 2003, v. 23, n. 2, p. 128, doi. 10.1002/pd.557

By:

Wieczorek, Dagmar;
Prott, Eva C.;
Robinson, Wendy P.;
Passarge, Eberhard;
Gillessen-Kaesbach, Gabriele

Publication type:

Article

No difference in expression of chromosomal fragile sites in patients with solid malignant tumours and normal controls.

Published in:

Genes, Chromosomes & Cancer, 1990, v. 2, n. 1, p. 44, doi. 10.1002/gcc.2870020108

By:

Kampmann, Thomas;
Schmidt, Angela;
Rüdiger, Hugo W.;
Tan, Tjhoen Lien;
Passarge, Eberhard

Publication type:

Article

Microcephaly, seizures, genital hypoplasia, and abnormalities of the hands and feet in a 4-year-old boy with possible Wiedemann syndrome.

Published in:

Clinical Genetics, 1996, v. 49, n. 2, p. 98, doi. 10.1111/j.1399-0004.1996.tb04337.x

By:

Wieczorek, Dagmar;
Gillessen-Kaesbach, Gabriele;
Plewa, Sven;
Passarge, Eberhard

Publication type:

Article

Der Weg in die Einheit: Das Fach Humangenetik 1990–1991. Ein Erfahrungsbericht.

Published in:

Medizinische Genetik, 2020, p. 275, doi. 10.1515/medgen-2020-2032

By:

Passarge, Eberhard;
Sperling, Karl;
Theile, Herbert

Publication type:

Article

Der Weg in die Einheit: Das Fach Humangenetik 1990–1991. Ein Erfahrungsbericht.

Published in:

Medizinische Genetik, 2020, p. 275, doi. 10.1515/medgen-2020-2032

By:

Passarge, Eberhard;
Sperling, Karl;
Theile, Herbert

Publication type:

Article

Molecular analysis and predictive testing in retinoblastoma.

Published in:

Ophthalmic Genetics, 1995, v. 16, n. 4, p. 135, doi. 10.3109/13816819509057854

By:

Lohmann, Dietmar R.;
Brandt, Birgit;
Oehlschläger, Ulrich;
Göttmann, Elke;
Höpping, Wolfgang;
Passarge, Eberhard;
Horsthemke, Bernhard

Publication type:

Article

Spectrum of small length germline mutations in the RB1 gene.

Published in:

Human Molecular Genetics, 1994, v. 3, n. 12, p. 2187

By:

Lohmann, Dletmar R.;
Brandt, Birglt;
Höpping, Wolfgang;
Passarge, Eberhard;
Horsthemke, Bernhard

Publication type:

Article

Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism.

Published in:

European Journal of Human Genetics, 1998, v. 6, n. 5, p. 432, doi. 10.1038/sj.ejhg.5200212

By:

Karadima, Georgia;
Bugge, Merete;
Nicolaidis, Peter;
Vassilopoulos, Dimitris;
Avramopoulos, Dimitris;
Grigoriadou, Maria;
Albrecht, Beate;
Passarge, Eberhard;
Annerén, Göran;
Blennow, Elisabeth;
Clausen, Niels;
Galla-Voumvouraki, Angeliki;
Tsezou, Aspasia;
Kitsiou-Tzeli, Sofia;
Hahnemann, Johanne M;
Hertz, Jens M;
Houge, Gunnar;
Kuklík, Miloslav;
Macek, Milan

Publication type:

Article

In memoriam James L. German, a pioneer in early human genetic research.

Published in:

American Journal of Medical Genetics. Part A, 2018, v. 176, n. 12, p. 2543, doi. 10.1002/ajmg.a.40513

By:

Groden, Joanna;
Passarge, Eberhard

Publication type:

Article

James L. German, a pioneer in early human genetic research turned 90.

Published in:

American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 6, p. 1564, doi. 10.1002/ajmg.a.37635

By:

Passarge, Eberhard

Publication type:

Article

Corrigendum: Transcriptional regulator PRDM12 is essential for human pain perception.

Published in:

Nature Genetics, 2015, v. 47, n. 8, p. 962, doi. 10.1038/ng0815-962b

By:

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

Publication type:

Article

Transcriptional regulator PRDM12 is essential for human pain perception.

Published in:

Nature Genetics, 2015, v. 47, n. 7, p. 803, doi. 10.1038/ng.3308

By:

Chen, Ya-Chun;
Stafford, Fay;
Nahorski, Michael S;
Shaikh, Samiha S;
Carvalho, Ofélia P;
Woods, C Geoffrey;
Schmid, Annina B;
Parman, Yesim;
Graul-Neumann, Luitgard;
Heinritz, Wolfram;
Passarge, Eberhard;
Watson, Rosemarie M;
McAleer, Maeve A;
Hertz, Jens Michael;
Moog, Ute;
Baumgartner, Manuela;
Valente, Enza Maria;
Auer-Grumbach, Michaela;
Schabhüttl, Maria;
Windhager, Reinhard

Publication type:

Article