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Wolfram Heinritz

Showing results (1-10 of 25) with videos related to

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Psychiatrische Praxis|March 13, 2010
[Risperidone intoxication in a patient with a genetic predisposition as "poor [non]metabolizer"]Maria Strauss, Wolfram Heinritz, Ulrich Hegerl, et al.
Journal of Pediatric Hematology/Oncology|May 9, 2006
Acute myelomonocytic leukemia in a boy with LEOPARD syndrome (PTPN11 gene mutation positive)Canan Uçar, Umran Calýskan, Susanne Martini, et al.
Human Mutation|September 1, 2005
The human TBX5 gene mutation databaseWolfram Heinritz, Lin Shou, Andre Moschik, et al.
Onkologie|January 16, 2009
Different phenotypes including gynecological cancer in three female patients with Peutz-Jeghers syndrome and mutations in the STK11 geneWolfram Heinritz, Sibylle Strenge, Annegret Kujat, et al.
Journal of Chromatographic Science|January 9, 2010
Evaluation of IP-RP-HPLC for length determination of the trinucleotide repeat fragments in Huntington's diseaseMarzena Skrzypczak, Wolfram Heinritz, Anna M Schulz, et al.
BMC Medical Genetics|December 1, 2014
Expanded spectrum of exon 33 and 34 mutations in SRCAP and follow-up in patients with Floating-Harbor syndromeWenke Seifert, Peter Meinecke, Gabriele Krüger, et al.
American Journal of Medical Genetics. Part A|December 4, 2004
Molecular and cytogenetic characterization of a non-mosaic isodicentric Y chromosome in a patient with Klinefelter syndromeWolfram Heinritz, Dieter Kotzot, Stefan Heinze, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 27, 2008
Macular corneal dystrophy: mutational spectrum in German patients, novel mutations and therapeutic optionsClaudia Gruenauer-Kloevekorn, Saskia Braeutigam, Wolfram Heinritz, et al.
Hereditary Cancer in Clinical Practice|March 13, 2010
MYH Gene Status in Polish FAP Patients without APC Gene MutationsMarzena Skrzypczak, Marta Podralska, Wolfram Heinritz, et al.
Human Mutation|March 19, 2005
Gene conversion between functional trypsinogen genes PRSS1 and PRSS2 associated with chronic pancreatitis in a six-year-old girlNiels Teich, Zsófia Nemoda, Henrik Köhler, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Psychiatrische Praxis|March 13, 2010
[Risperidone intoxication in a patient with a genetic predisposition as "poor [non]metabolizer"]Maria Strauss, Wolfram Heinritz, Ulrich Hegerl, et al.
Journal of Pediatric Hematology/Oncology|May 9, 2006
Acute myelomonocytic leukemia in a boy with LEOPARD syndrome (PTPN11 gene mutation positive)Canan Uçar, Umran Calýskan, Susanne Martini, et al.
Human Mutation|September 1, 2005
The human TBX5 gene mutation databaseWolfram Heinritz, Lin Shou, Andre Moschik, et al.
Onkologie|January 16, 2009
Different phenotypes including gynecological cancer in three female patients with Peutz-Jeghers syndrome and mutations in the STK11 geneWolfram Heinritz, Sibylle Strenge, Annegret Kujat, et al.
Journal of Chromatographic Science|January 9, 2010
Evaluation of IP-RP-HPLC for length determination of the trinucleotide repeat fragments in Huntington's diseaseMarzena Skrzypczak, Wolfram Heinritz, Anna M Schulz, et al.
BMC Medical Genetics|December 1, 2014
Expanded spectrum of exon 33 and 34 mutations in SRCAP and follow-up in patients with Floating-Harbor syndromeWenke Seifert, Peter Meinecke, Gabriele Krüger, et al.
American Journal of Medical Genetics. Part A|December 4, 2004
Molecular and cytogenetic characterization of a non-mosaic isodicentric Y chromosome in a patient with Klinefelter syndromeWolfram Heinritz, Dieter Kotzot, Stefan Heinze, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 27, 2008
Macular corneal dystrophy: mutational spectrum in German patients, novel mutations and therapeutic optionsClaudia Gruenauer-Kloevekorn, Saskia Braeutigam, Wolfram Heinritz, et al.
Hereditary Cancer in Clinical Practice|March 13, 2010
MYH Gene Status in Polish FAP Patients without APC Gene MutationsMarzena Skrzypczak, Marta Podralska, Wolfram Heinritz, et al.
Human Mutation|March 19, 2005
Gene conversion between functional trypsinogen genes PRSS1 and PRSS2 associated with chronic pancreatitis in a six-year-old girlNiels Teich, Zsófia Nemoda, Henrik Köhler, et al.
Pageof 3