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Heidemarie Neitzel
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Journal Articles

A case of paroxysmal nocturnal hemoglobinuria caused by a germline mutation and a somatic mutation in PIGT

Brief Report
Peter M. Krawitz, Britta Höchsmann, Yoshiko Murakami, Britta Teubner, Ulrike Krüger, Eva Klopocki, Heidemarie Neitzel, Alexander Hoellein, Christina Schneider, Dmitri Parkhomchuk, Jochen Hecht, Peter N. Robinson, Stefan Mundlos, Taroh Kinoshita, Hubert Schrezenmeier
Journal: Blood
Blood (2013) 122 (7): 1312–1315.
https://doi.org/10.1182/blood-2013-01-481499
Published: 2013
Includes: Supplemental data
Journal Articles

Fanconi anemia (FA)–associated 3q gains in leukemic transformation consistently target EVI1 , but do not affect low TERC expression in FA

Stefan Meyer, Claire Bristow, Mark Wappett, Stuart Pepper, Anthony D. Whetton, Helmut Hanenberg, Heidemarie Neitzel, Marcin W. Wlodarski, Wolfram Ebell, Holger Tönnies
Journal: Blood
Blood (2011) 117 (22): 6047–6050.
https://doi.org/10.1182/blood-2011-03-343897
Published: 2011
Includes: Supplemental data
Journal Articles

SNP-Array Karyotyping Reveals the Presence of Previously Cryptic Clonal Chromosomal Aberrations Including Segmental UPD in Patients with Fanconi Anemia.

Marcin Wlodarski, MS, Holger Toennies, PhD, Andrew Dunbar, Zach Nearman, Marion Nagy, PhD, Joern-Sven Kuehl, MD, Heidemarie Neitzel, PhD, Wolfram Ebell, MD, Jaroslaw Maciejewski, MD
Journal: Blood
Blood (2007) 110 (11): 1678.
https://doi.org/10.1182/blood.V110.11.1678.1678
Published: 2007
Journal Articles

Clonal chromosomal aberrations in bone marrow cells of Fanconi anemia patients: gains of the chromosomal segment 3q26q29 as an adverse risk factor

Clinical Trials & Observations Brief Report
Holger Tönnies, Stefanie Huber, Jörn-Sven Kühl, Antje Gerlach, Wolfram Ebell, Heidemarie Neitzel
Journal: Blood
Blood (2003) 101 (10): 3872–3874.
https://doi.org/10.1182/blood-2002-10-3243
Published: 2003