Publications by authors named "Inka Praulich"

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Phenotypic spectrum of BLM- and RMI1-related Bloom syndrome.
Ipek Ilgin Gönenc, Nursel H Elcioglu, Carolina Martinez Grijalva, Seda Aras, Nadine Großmann, Inka Praulich

Clin Genet· May 2022

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Molecular characterization of the rare translocation t(3;10)(q26;q21) in an acute myeloid leukemia patient.
Tereza Jancuskova, Radek Plachy, Lucie Zemankova, David Warren Hardekopf, Jiri Stika, Inka Praulich

Mol Cytogenet· July 2014

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Array-CGH in childhood MDS.
Marcel Tauscher, Inka Praulich, Doris Steinemann

Methods Mol Biol· July 2013

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Patient-specific analysis of FLT3 internal tandem duplications for the prognostication and monitoring of acute myeloid leukemia.
Joanna Schiller, Inka Praulich, Cristiano Krings Rocha, Karl-Anton Kreuzer

Eur J Haematol· July 2012

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Constitutional trisomy 8p11.21-q11.21 mosaicism: a germline alteration predisposing to myeloid leukaemia.
Tim Ripperger, Marcel Tauscher, Inka Praulich, Brigitte Pabst, Andrea Teigler-Schlegel

Br J Haematol· October 2011

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A rare case of t(11;22) in a mantle cell lymphoma like B-cell neoplasia resulting in a fusion of IGL and CCND1: case report.
Cristiano Krings Rocha, Inka Praulich, Iris Gehrke, Michael Hallek, Karl-Anton Kreuzer

Mol Cytogenet· April 2011

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Clonal heterogeneity in childhood myelodysplastic syndromes--challenge for the detection of chromosomal imbalances by array-CGH.
Inka Praulich, Marcel Tauscher, Gudrun Göhring, Stefanie Glaser, Winfried Hofmann

Genes Chromosomes Cancer· October 2010

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Mutations in the let-7 binding site - a mechanism of RAS activation in juvenile myelomonocytic leukemia?
Doris Steinemann, Marcel Tauscher, Inka Praulich, Charlotte M Niemeyer, Christian Flotho

Haematologica· September 2010

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Mitotic recombination and compound-heterozygous mutations are predominant NF1-inactivating mechanisms in children with juvenile myelomonocytic leukemia and neurofibromatosis type 1.
Doris Steinemann, Larissa Arning, Inka Praulich, Manfred Stuhrmann, Henrik Hasle

Haematologica· February 2010

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Mutation analysis of the HAX1 gene in childhood myelodysplastic syndrome.
Doris Steinemann, Inka Praulich, Noreen Otto, Gudrun Göhring, Charlotte M Niemeyer

Br J Haematol· May 2009

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