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Prognostic Impact of Specific Chromosomal Aberrations in a Large Group of Pediatric Patients With Acute Myeloid Leukemia Treated Uniformly According to Trial AML-BFM 98

Journal of clinical oncology, 2010-06, Vol.28 (16), p.2682-2689

2010

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Ataxia-telangiectasia mutated (ATM) silencing promotes neuroblastoma progression through a MYCN independent mechanism

Oncotarget, 2015-07, Vol.6 (21), p.18558-18576

2015

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NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families

European journal of medical genetics, 2019-03, Vol.62 (3), p.204-209

2019

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Similar but different: identical pathology with differing outcome in ‘Not‐so‐identical’ twins

British journal of haematology, 2017-07, Vol.178 (1), p.152-153

2017

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Early Bilateral Gonadoblastoma in a Young Child with Mosaicism for Turner Syndrome and Trisomy 18 with Y Chromosome

Hormone research in paediatrics, 2017-01, Vol.87 (2), p.130-135

2017

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A case report of primary ciliary dyskinesia, laterality defects and developmental delay caused by the co-existence of a single gene and chromosome disorder

BMC medical genetics, 2015-06, Vol.16 (1), p.45-45, Article 45

2015

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CBFB-SMMHC is correlated with increased calreticulin expression and suppresses the granulocytic differentiation factor CEBPA in AML with inv(16)

Blood, 2005-08, Vol.106 (4), p.1369-1375

2005

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A new and a reclassified ICF patient without mutations in DNMT3B and its interacting proteins SUMO-1 and UBC9

American journal of medical genetics. Part A, 2005-07, Vol.136A (1), p.31-37

2005

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Cytogenetic characterization of childhood acute lymphoblastic leukemia in Nicaragua

Pediatric blood & cancer, 2009-12, Vol.53 (7), p.1238-1241

2009

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High-resolution Genome-wide Copy-number Analyses Identify Localized Copy-number Alterations in Ewing Sarcoma

Diagnostic molecular pathology, 2013-06, Vol.22 (2), p.76-84

2013

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The PAX5 oncogene is expressed in N-type neuroblastoma cells and increases tumorigenicity of a S-type cell line

Carcinogenesis (New York), 2004-10, Vol.25 (10), p.1839-1846

2004

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The prognostic significance of cytogenetic aberrations in childhood acute myeloid leukaemia. A study of the Swiss Paediatric Oncology Group (SPOG)

European journal of haematology, 2007-06, Vol.78 (6), p.468-476

2007

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SKY reveals a high frequency of unbalanced translocations involving chromosome 6 in t(12;21)-positive acute lymphoblastic leukemia

Leukemia research, 2008-01, Vol.32 (1), p.39-43

2008

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ATM promoter analysis in childhood lymphoid malignancies: A brief communication

Leukemia research, 2006-03, Vol.30 (3), p.335-337

2006

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Clonal expansion of a new MLL rearrangement in the absence of leukemia

Blood, 2005-05, Vol.105 (10), p.4151-4152

2005

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Characterization of karyotypic events and evolution in neuroblastoma

Pediatric Blood & Cancer, 2005-02, Vol.44 (2), p.147-157

2005

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Constitutional balanced chromosomal rearrangements and neoplasm in children

Journal of pediatric hematology/oncology, 2001-12, Vol.23 (9), p.582-584

2001

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Inv(11)(p13p15) and Myf-3(MyoD1) in a malignant extrarenal rhabdoid tumor of a premature newborn

Pediatric research, 2000-10, Vol.48 (4), p.463-467

2000

Volltextzugriff (PDF)

Involvement of der(12)t(12;21)(p13;q22) and as well as additional rearrangements of chromosome 12 homolog in ETV6/RUNX1 -positive acute lymphoblastic leukemia

Cancer genetics and cytogenetics, 2009-04, Vol.190 (1), p.26-32

2009

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ATM alterations in childhood non-Hodgkin lymphoma

Cancer genetics and cytogenetics, 2006-04, Vol.166 (2), p.101-111

2006

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Detection of unidentified chromosome abnormalities in human neuroblastoma by spectral karyotyping (SKY)

Genes chromosomes & cancer, 2001-07, Vol.31 (3), p.201-208

2001

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Non-classical karyotypic features in relapsed childhood B-cell precursor acute lymphoblastic leukemia

Cancer genetics and cytogenetics, 2009-02, Vol.189 (1), p.29-36

2009

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Cytogenetic characterization of Ewing tumors with high-ploidy

Cancer genetics and cytogenetics, 2005-06, Vol.159 (2), p.160-163

2005

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Routine Karyotyping in Wilms Tumor

Cancer genetics and cytogenetics, 1997-07, Vol.96 (2), p.151-156

1997

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Deletion 14q (q22q23) associated with anophthalmia, absent pituitary, and other abnormalities

Journal of medical genetics, 1991-04, Vol.28 (4), p.280-281

1991

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Prognostic Impact of Specific Chromosomal Aberrations in a Large Group of Pediatric Patients With Acute Myeloid Leukemia Treated Uniformly According to Trial AML-BFM 98

Ataxia-telangiectasia mutated (ATM) silencing promotes neuroblastoma progression through a MYCN independent mechanism

NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families

Similar but different: identical pathology with differing outcome in ‘Not‐so‐identical’ twins

Early Bilateral Gonadoblastoma in a Young Child with Mosaicism for Turner Syndrome and Trisomy 18 with Y Chromosome

A case report of primary ciliary dyskinesia, laterality defects and developmental delay caused by the co-existence of a single gene and chromosome disorder

CBFB-SMMHC is correlated with increased calreticulin expression and suppresses the granulocytic differentiation factor CEBPA in AML with inv(16)

A new and a reclassified ICF patient without mutations in DNMT3B and its interacting proteins SUMO-1 and UBC9

Cytogenetic characterization of childhood acute lymphoblastic leukemia in Nicaragua

High-resolution Genome-wide Copy-number Analyses Identify Localized Copy-number Alterations in Ewing Sarcoma

The PAX5 oncogene is expressed in N-type neuroblastoma cells and increases tumorigenicity of a S-type cell line

The prognostic significance of cytogenetic aberrations in childhood acute myeloid leukaemia. A study of the Swiss Paediatric Oncology Group (SPOG)

SKY reveals a high frequency of unbalanced translocations involving chromosome 6 in t(12;21)-positive acute lymphoblastic leukemia

ATM promoter analysis in childhood lymphoid malignancies: A brief communication

Clonal expansion of a new MLL rearrangement in the absence of leukemia

Characterization of karyotypic events and evolution in neuroblastoma

Constitutional balanced chromosomal rearrangements and neoplasm in children

Inv(11)(p13p15) and Myf-3(MyoD1) in a malignant extrarenal rhabdoid tumor of a premature newborn

Involvement of der(12)t(12;21)(p13;q22) and as well as additional rearrangements of chromosome 12 homolog in ETV6/RUNX1 -positive acute lymphoblastic leukemia

ATM alterations in childhood non-Hodgkin lymphoma

Detection of unidentified chromosome abnormalities in human neuroblastoma by spectral karyotyping (SKY)

Non-classical karyotypic features in relapsed childhood B-cell precursor acute lymphoblastic leukemia

Cytogenetic characterization of Ewing tumors with high-ploidy

Routine Karyotyping in Wilms Tumor

Deletion 14q (q22q23) associated with anophthalmia, absent pituitary, and other abnormalities

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