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Prognostic impact of chromosomal aberrations in Ewing tumours

British journal of cancer, 2002-06, Vol.86 (11), p.1763-1769

2002

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Prenatal origin of separate evolution of leukemia in identical twins

Leukemia, 2004-10, Vol.18 (10), p.1624-1629

2004

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Cytogenetic abnormalities in Langerhans cell histiocytosis

British journal of cancer, 1998-02, Vol.77 (4), p.552-555

1998

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X-linked moyamoya syndrome associated with severe haemophilia A

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-01, Vol.22 (1), p.e51-e54

2016

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Unexplained developmental delay/learning disability: guidelines for best practice protocol for first line assessment and genetic/metabolic/radiological investigations

Irish journal of medical science, 2016-02, Vol.185 (1), p.241-248

2016

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ATM variants and predisposition to childhood T-lineage acute lymphoblastic leukaemia

Leukemia, 2006-03, Vol.20 (3), p.526-527

2006

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Duplication of 17q11.2 and Features of Albright Hereditary Osteodystrophy Secondary to Methylation Defects within the GNAS Cluster: Coincidence or Causal?

Case reports in genetics, 2013-01, Vol.2013, p.764152-3

2013

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Molecular features of a human rhabdomyosarcoma cell line with spontaneous metastatic progression

British journal of cancer, 2000-03, Vol.82 (6), p.1239-1245

2000

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Isolated follicular lymphoma cells are resistant to apoptosis and can be grown in vitro in the CD40/stromal cell system

Blood, 1993-09, Vol.82 (6), p.1848-1857

1993

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A simple FISH assay for the detection of 3q26 rearrangements in myeloid malignancy

Leukemia, 2008-02, Vol.22 (2), p.434-437

2008

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Cytogenetics in acute myeloid leukaemia

Blood reviews, 1994-03, Vol.8 (1), p.30-36

1994

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Abnormalities of chromosome 16q in myeloid malignancy : 14 new cases and a review of the literature

Leukemia, 1992-12, Vol.6 (12), p.1250-1256

1992

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The Investigation of Karyotypic Instability in the High-Hyperdiploidy Subgroup of Acute Lymphoblastic Leukemia

Leukemia & lymphoma, 2001, Vol.42 (1-2), p.187-193

2001

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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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Primary pleomorphic adenoma of the external auditory canal diagnosed by fine needle aspiration cytology : A case report

Acta cytologica, 1999-05, Vol.43 (3), p.489-491

1999

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Gain of Chromosome Arm 17q and Adverse Outcome in Patients with Neuroblastoma

The New England journal of medicine, 1999-06, Vol.340 (25), p.1954-1961

1999

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Frequency and Prognostic Impact of ALK Amplifications and Mutations in the European Neuroblastoma Study Group (SIOPEN) High-Risk Neuroblastoma Trial (HR-NBL1)

Journal of clinical oncology, 2021-10, Vol.39 (30), p.3377-3390

2021

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A further case of a t(11;20)(p15;q11.2) translocation in an acute myeloid leukemia (FAB M2)

Journal of pediatric hematology/oncology, 1998, Vol.20 (1), p.91-93

1998

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Monosomy 7, Diabetes Insipidus and Acute Myeloid Leukemia in Childhood

Pediatric hematology and oncology, 1994, Vol.11 (1), p.111-114

1994

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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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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

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Evaluation of subcutaneous implantable cardioverter-defibrillator performance in patients with ion channelopathies from the EFFORTLESS cohort and comparison with a meta-analysis of transvenous ICD outcomes

Heart rhythm O2, 2020-12, Vol.1 (5), p.326-335

2020

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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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Prognostic impact of chromosomal aberrations in Ewing tumours

Prenatal origin of separate evolution of leukemia in identical twins

Cytogenetic abnormalities in Langerhans cell histiocytosis

X-linked moyamoya syndrome associated with severe haemophilia A

Unexplained developmental delay/learning disability: guidelines for best practice protocol for first line assessment and genetic/metabolic/radiological investigations

ATM variants and predisposition to childhood T-lineage acute lymphoblastic leukaemia

Duplication of 17q11.2 and Features of Albright Hereditary Osteodystrophy Secondary to Methylation Defects within the GNAS Cluster: Coincidence or Causal?

Molecular features of a human rhabdomyosarcoma cell line with spontaneous metastatic progression

Isolated follicular lymphoma cells are resistant to apoptosis and can be grown in vitro in the CD40/stromal cell system

A simple FISH assay for the detection of 3q26 rearrangements in myeloid malignancy

Cytogenetics in acute myeloid leukaemia

Abnormalities of chromosome 16q in myeloid malignancy : 14 new cases and a review of the literature

The Investigation of Karyotypic Instability in the High-Hyperdiploidy Subgroup of Acute Lymphoblastic Leukemia

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

Primary pleomorphic adenoma of the external auditory canal diagnosed by fine needle aspiration cytology : A case report

Gain of Chromosome Arm 17q and Adverse Outcome in Patients with Neuroblastoma

Frequency and Prognostic Impact of ALK Amplifications and Mutations in the European Neuroblastoma Study Group (SIOPEN) High-Risk Neuroblastoma Trial (HR-NBL1)

A further case of a t(11;20)(p15;q11.2) translocation in an acute myeloid leukemia (FAB M2)

Monosomy 7, Diabetes Insipidus and Acute Myeloid Leukemia in Childhood

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

Constitutional balanced chromosomal rearrangements and neoplasm in children

Impact of acute atrial fibrillation termination and prolongation of atrial fibrillation cycle length on the outcome of ablation of persistent atrial fibrillation: A substudy of the STAR AF II trial

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

Evaluation of subcutaneous implantable cardioverter-defibrillator performance in patients with ion channelopathies from the EFFORTLESS cohort and comparison with a meta-analysis of transvenous ICD outcomes

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

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