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Heidemarie Neitzel

Showing results (11-20 of 54) with videos related to

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Prenatal Diagnosis|March 1, 2006
Prenatal diagnosis and molecular cytogenetic characterisation of a small de novo interstitial duplication 16q11.2-q13Marc Trimborn, Rolf-Dieter Wegner, Holger Tönnies, et al.
Blood|January 4, 2003
Clonal chromosomal aberrations in bone marrow cells of Fanconi anemia patients: gains of the chromosomal segment 3q26q29 as an adverse risk factorHolger Tönnies, Stefanie Huber, Jörn-Sven Kuhl, et al.
Proteomics|June 30, 2005
A two-dimensional electrophoretic map of human mitochondrial proteins from immortalized lymphoblastoid cell lines: a prerequisite to study mitochondrial disorders in patientsJing Xie, Sandra Techritz, Sophie Haebel, et al.
American Journal of Medical Genetics. Part A|February 25, 2003
Familial MCA/MR syndrome due to inherited submicroscopic translocation t(18;21)(q22.1q21.3) with breakpoint at the Down syndrome critical regionDenise Horn, Heidemarie Neitzel, Holger Tönnies, et al.
The Journal of Cell Biology|September 14, 2011
MCPH1 regulates chromosome condensation and shaping as a composite modulator of condensin IIDaisuke Yamashita, Keishi Shintomi, Takao Ono, et al.
Pediatric Hematology and Oncology|February 23, 2016
Androgen therapy in Fanconi anemia: A retrospective analysis of 30 years in GermanyLaura Paustian, Mwe Mwe Chao, Helmut Hanenberg, et al.
Cytogenetic and Genome Research|March 5, 2026
Familial Robertsonian Translocation, rob(14;21), with high risk for Down syndromeAnna Rajab, Heidemarie Neitzel, Jenny Jalali, et al.
Clinical Dysmorphology|May 31, 2012
Holoprosencephaly-polydactyly/pseudotrisomy 13: a presentation of two new cases and a review of the literatureSophia M Bous, Benjamin D Solomon, Luitgard Graul-Neumann, et al.
American Journal of Medical Genetics. Part A|June 24, 2004
Minimal clinical expression of the holoprosencephaly spectrum and of Currarino syndrome due to different cytogenetic rearrangements deleting the Sonic Hedgehog gene and the HLXB9 gene at 7q36.3Denise Horn, Holger Tönnies, Heidemarie Neitzel, et al.
American Journal of Medical Genetics. Part A|January 24, 2009
Interstitial deletion 2p11.2-p12: report of a patient with mental retardation and review of the literatureAndreas Tzschach, Luitgard M Graul-Neumann, Kateryna Konrat, et al.
Pageof 6

Showing results (11-20 of 54) with videos related to

Sort By:
Pageof 6
Prenatal Diagnosis|March 1, 2006
Prenatal diagnosis and molecular cytogenetic characterisation of a small de novo interstitial duplication 16q11.2-q13Marc Trimborn, Rolf-Dieter Wegner, Holger Tönnies, et al.
Blood|January 4, 2003
Clonal chromosomal aberrations in bone marrow cells of Fanconi anemia patients: gains of the chromosomal segment 3q26q29 as an adverse risk factorHolger Tönnies, Stefanie Huber, Jörn-Sven Kuhl, et al.
Proteomics|June 30, 2005
A two-dimensional electrophoretic map of human mitochondrial proteins from immortalized lymphoblastoid cell lines: a prerequisite to study mitochondrial disorders in patientsJing Xie, Sandra Techritz, Sophie Haebel, et al.
American Journal of Medical Genetics. Part A|February 25, 2003
Familial MCA/MR syndrome due to inherited submicroscopic translocation t(18;21)(q22.1q21.3) with breakpoint at the Down syndrome critical regionDenise Horn, Heidemarie Neitzel, Holger Tönnies, et al.
The Journal of Cell Biology|September 14, 2011
MCPH1 regulates chromosome condensation and shaping as a composite modulator of condensin IIDaisuke Yamashita, Keishi Shintomi, Takao Ono, et al.
Pediatric Hematology and Oncology|February 23, 2016
Androgen therapy in Fanconi anemia: A retrospective analysis of 30 years in GermanyLaura Paustian, Mwe Mwe Chao, Helmut Hanenberg, et al.
Cytogenetic and Genome Research|March 5, 2026
Familial Robertsonian Translocation, rob(14;21), with high risk for Down syndromeAnna Rajab, Heidemarie Neitzel, Jenny Jalali, et al.
Clinical Dysmorphology|May 31, 2012
Holoprosencephaly-polydactyly/pseudotrisomy 13: a presentation of two new cases and a review of the literatureSophia M Bous, Benjamin D Solomon, Luitgard Graul-Neumann, et al.
American Journal of Medical Genetics. Part A|June 24, 2004
Minimal clinical expression of the holoprosencephaly spectrum and of Currarino syndrome due to different cytogenetic rearrangements deleting the Sonic Hedgehog gene and the HLXB9 gene at 7q36.3Denise Horn, Holger Tönnies, Heidemarie Neitzel, et al.
American Journal of Medical Genetics. Part A|January 24, 2009
Interstitial deletion 2p11.2-p12: report of a patient with mental retardation and review of the literatureAndreas Tzschach, Luitgard M Graul-Neumann, Kateryna Konrat, et al.
Pageof 6