International recommendations and guidelines for the safe use of diagnostic ultrasound in medicine
Barnett, Stanley B, Ter Haar, Gail R, Ziskin, Marvin C, Rott, Hans-Dieter, Duck, Francis A, Maeda, Kazuo
Published in Ultrasound in Medicine & Biology (01.03.2000)
Published in Ultrasound in Medicine & Biology (01.03.2000)
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Book Review
Journal Article
The sensitivity of biological tissue to ultrasound
Barnett, Stanley B., Rott, Hans-Dieter, ter Haar, Gail R., Ziskin, Marvin C., Maeda, Kazuo
Published in Ultrasound in Medicine & Biology (1997)
Published in Ultrasound in Medicine & Biology (1997)
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Book Review
Journal Article
Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation
TEBER, Özge Altug, GILLESSEN-KAESBACH, Gabriele, HENN, Wolfram, HINKEL, Georg Klaus, KÖNIG, Rainer, KUNSTMANN, Erdmute, KUNZE, Jürgen, NEUMANN, Luitgard M, PROTT, Eva-Christina, RAUCH, Anita, ROTT, Hans-Dieter, SEIDEL, Heide, FISCHER, Sven, SPRANGER, Stephanie, SPRENGEL, Martin, ZOLL, Barbara, LOHMANN, Dietmar R, WIECZOREK, Dagmar, BÖHRINGER, Stefan, ALBRECHT, Beate, ALBERT, Angelika, ARSLAN-KIRCHNER, Mine, HAAN, Eric, HAGEDORN-GREIWE, Monika, HAMMANS, Christof
Published in European journal of human genetics : EJHG (01.11.2004)
Published in European journal of human genetics : EJHG (01.11.2004)
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Journal Article
Mutations in the ZNF41 Gene Are Associated with Cognitive Deficits: Identification of a New Candidate for X-Linked Mental Retardation
Shoichet, Sarah A., Hoffmann, Kirsten, Menzel, Corinna, Trautmann, Udo, Moser, Bettina, Hoeltzenbein, Maria, Echenne, Bernard, Partington, Michael, van Bokhoven, Hans, Moraine, Claude, Fryns, Jean-Pierre, Chelly, Jamel, Rott, Hans-Dieter, Ropers, Hans-Hilger, Kalscheuer, Vera M.
Published in American journal of human genetics (01.12.2003)
Published in American journal of human genetics (01.12.2003)
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Journal Article
"Mowat-Wilson" syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene
Zweier, Christiane, Albrecht, Beate, Mitulla, Beate, Behrens, Rolf, Beese, Maike, Gillessen-Kaesbach, Gabriele, Rott, Hans-Dieter, Rauch, Anita
Published in American journal of medical genetics (15.03.2002)
Published in American journal of medical genetics (15.03.2002)
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Journal Article
Cyst-like cerebral lesions in tuberous sclerosis
Rott, Hans-Dieter, Lemcke, Beate, Zenker, Martin, Huk, Walter, Horst, Jürgen, Mayer, Karin
Published in American journal of medical genetics (01.09.2002)
Published in American journal of medical genetics (01.09.2002)
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Journal Article
Mosaicism for the Charcot-Marie-Tooth disease type 1A duplication suggests somatic reversion
Liehr, T, Rautenstrauss, B, Grehl, H, Bathke, K D, Ekici, A, Rauch, A, Rott, H D
Published in Human genetics (01.07.1996)
Published in Human genetics (01.07.1996)
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