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Oliver Bartsch

Showing results (81-90 of 118) with videos related to

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European Journal of Nuclear Medicine and Molecular Imaging|February 5, 2013
High incidence of extraadrenal paraganglioma in families with SDHx syndromes detected by functional imaging with [18F]fluorodihydroxyphenylalanine PETMatthias Miederer, Christian Fottner, Heidi Rossmann, et al.
European Journal of Medical Genetics|September 24, 2005
Small reciprocal insertion detected by spectral karyotyping (SKY) and delimited by array-CGH analysisAnja Matthaei, Walter Werner, Eva-Maria Gerlach, et al.
European Journal of Human Genetics : EJHG|May 30, 2013
Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6Simone Rost, Elisa Bach, Cordula Neuner, et al.
Journal of Pediatric Urology|May 4, 2007
DELETION MAPPING OF CRITICAL REGION FOR HYPOSPADIAS, PENOSCROTAL TRANSPOSITION AND IMPERFORATE ANUS ON HUMAN CHROMOSOME 13Nilda M Garcia, Jocelyn Allgood, Lane J Santos, et al.
European Journal of Medical Genetics|January 25, 2019
Heterotopic ossifications and Charcot joints: Congenital insensitivity to pain with anhidrosis (CIPA) and a novel NTRK1 gene mutationZoran Gucev, Velibor Tasic, Ivona Bogevska, et al.
Clinical Dysmorphology|April 2, 2004
Hypertrichosis, hyperkeratosis, abnormal corpus callosum, mental retardation and dysmorphic features in three unrelated femalesMinna H Pöyhönen, Maarit M Peippo, Leena K Valanne, et al.
Frontiers in Immunology|November 3, 2023
Case Report: Targeting of individual somatic tumor mutations by multipeptide vaccination tailored for HLA class I and II presentation induces strong CD4 and CD8 T-cell responses in a patient with metastatic castration sensitive prostate cancerHenning Zelba, Armin Rabsteyn, Oliver Bartsch, et al.
Epigenetics|December 31, 2011
Monozygotic twins discordant for constitutive BRCA1 promoter methylation, childhood cancer and secondary cancerDanuta Galetzka, Tamara Hansmann, Nady El Hajj, et al.
Plos One|October 13, 2011
Reduced mRNA and protein expression of the genomic caretaker RAD9A in primary fibroblasts of individuals with childhood and independent second cancerEva Weis, Holger Schoen, Anja Victor, et al.
Clinical Genetics|June 10, 2024
Expanding the spectrum of phenotypes for MPDZ: Report of four unrelated families and review of the literatureAboulfazl Rad, Oliver Bartsch, Somayeh Bakhtiari, et al.
Pageof 12

Showing results (81-90 of 118) with videos related to

Sort By:
Pageof 12
European Journal of Nuclear Medicine and Molecular Imaging|February 5, 2013
High incidence of extraadrenal paraganglioma in families with SDHx syndromes detected by functional imaging with [18F]fluorodihydroxyphenylalanine PETMatthias Miederer, Christian Fottner, Heidi Rossmann, et al.
European Journal of Medical Genetics|September 24, 2005
Small reciprocal insertion detected by spectral karyotyping (SKY) and delimited by array-CGH analysisAnja Matthaei, Walter Werner, Eva-Maria Gerlach, et al.
European Journal of Human Genetics : EJHG|May 30, 2013
Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6Simone Rost, Elisa Bach, Cordula Neuner, et al.
Journal of Pediatric Urology|May 4, 2007
DELETION MAPPING OF CRITICAL REGION FOR HYPOSPADIAS, PENOSCROTAL TRANSPOSITION AND IMPERFORATE ANUS ON HUMAN CHROMOSOME 13Nilda M Garcia, Jocelyn Allgood, Lane J Santos, et al.
European Journal of Medical Genetics|January 25, 2019
Heterotopic ossifications and Charcot joints: Congenital insensitivity to pain with anhidrosis (CIPA) and a novel NTRK1 gene mutationZoran Gucev, Velibor Tasic, Ivona Bogevska, et al.
Clinical Dysmorphology|April 2, 2004
Hypertrichosis, hyperkeratosis, abnormal corpus callosum, mental retardation and dysmorphic features in three unrelated femalesMinna H Pöyhönen, Maarit M Peippo, Leena K Valanne, et al.
Frontiers in Immunology|November 3, 2023
Case Report: Targeting of individual somatic tumor mutations by multipeptide vaccination tailored for HLA class I and II presentation induces strong CD4 and CD8 T-cell responses in a patient with metastatic castration sensitive prostate cancerHenning Zelba, Armin Rabsteyn, Oliver Bartsch, et al.
Epigenetics|December 31, 2011
Monozygotic twins discordant for constitutive BRCA1 promoter methylation, childhood cancer and secondary cancerDanuta Galetzka, Tamara Hansmann, Nady El Hajj, et al.
Plos One|October 13, 2011
Reduced mRNA and protein expression of the genomic caretaker RAD9A in primary fibroblasts of individuals with childhood and independent second cancerEva Weis, Holger Schoen, Anja Victor, et al.
Clinical Genetics|June 10, 2024
Expanding the spectrum of phenotypes for MPDZ: Report of four unrelated families and review of the literatureAboulfazl Rad, Oliver Bartsch, Somayeh Bakhtiari, et al.
Pageof 12