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A mixture model of nuchal translucency thickness in screening for chromosomal defects: validation of a single operator dataset

Prenatal diagnosis, 2010-11, Vol.30 (11), p.1100-1106

2010

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First-Trimester Prenatal Diagnosis of Okihiro Syndrome

Fetal diagnosis and therapy, 2010-01, Vol.27 (4), p.222-226

2010

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Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probes

Journal of medical genetics, 2002-06, Vol.39 (6), p.434-439

2002

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Impaired p53-mediated DNA damage response, cell-cycle disturbance and chromosome aberrations in Nijmegen breakage syndrome lymphoblastoid cell lines

International journal of radiation biology, 1999, Vol.75 (5), p.583-591

ANTOCCIA, M. STUMM, K. SAAR, R. RICORDY, P. MARASCHIO, C. TANZARELLA, A.

1999

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High frequency of spontaneous translocations revealed by FISH in cells from patients with the cancer-prone syndromes ataxia telangiectasia and Nijmegen breakage syndrome

Cytogenetics and cell genetics, 2001, Vol.92 (3-4), p.186

2001

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Multi-locus (ML)-FISH is a reliable tool for nondisjunction studies in human oocytes

Cytogenetic and genome research, 2003, Vol.103 (1-2), p.47-53

2003

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STI571 Enhances the Therapeutic Index of Epothilone B by a Tumor-selective Increase of Drug Uptake

Clinical cancer research, 2003-09, Vol.9 (10), p.3779-3787

2003

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Improved definition of chromosomal breakpoints using high-resolution multicolour banding

Human genetics, 2001-06, Vol.108 (6), p.478-483

2001

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Frequency of CFTR gene mutations in males participating in an ICSI programme

Human reproduction (Oxford), 1999-07, Vol.14 (7), p.1833-1834

1999

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Heterozygous Submicroscopic Inversions Involving Olfactory Receptor–Gene Clusters Mediate the Recurrent t(4;8)(p16;p23) Translocation

American journal of human genetics, 2002-08, Vol.71 (2), p.276-285

2002

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Patupilone Induced Vascular Disruption in Orthotopic Rodent Tumor Models Detected by Magnetic Resonance Imaging and Interstitial Fluid Pressure

Clinical cancer research, 2005-11, Vol.11 (21), p.7773-7784

2005

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Increased cancer risk of heterozygotes with NBS1 germline mutations in poland

International journal of cancer, 2004-08, Vol.111 (1), p.67-71

2004

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No evidence for a major role of heterozygous deletion 657del5 within the NBS1 gene in the pathogenesis of non‐Hodgkin's lymphoma of childhood and adolescence

British journal of haematology, 2000-04, Vol.109 (1), p.117-120

2000

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Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnostics

Cytogenetics and cell genetics, 2001, Vol.93 (3-4), p.188

2001

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Molecular characterization of the DICE1 (DDX26) tumor suppressor gene in lung carcinoma cells

Oncology research, 2001-01, Vol.12 (11-12), p.491

2001

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High reliability and sensitivity of the BCR/ABL1 D-FISH test for the detection of BCR/ABL rearrangements

Annals of hematology, 2002-03, Vol.81 (3), p.147-153

2002

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Attenuation of the formation of DNA-repair foci containing RAD51 in Fanconi anaemia

Carcinogenesis (New York), 2002-07, Vol.23 (7), p.1121-1126

2002

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Molecular cytogenetic techniques for the diagnosis of chromosomal abnormalities in childhood disease

European journal of pediatrics, 1999-07, Vol.158 (7), p.531-536

1999

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Mosaic tetrasomy 9p in a girl with multiple congenital anomalies : cytogenetic and molecular-cytogenetic studies

European journal of pediatrics, 1999-07, Vol.158 (7), p.571-575

1999

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Radiosensitivity of Ataxia Telangiectasia and Nijmegen Breakage Syndrome Homozygotes and Heterozygotes as Determined by Three-Color FISH Chromosome Painting

Radiation research, 2002-03, Vol.157 (3), p.312-321

2002

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Mutations of the gene encoding the transmembrane transporter protein ABC-C6 cause pseudoxanthoma elasticum

Journal of molecular medicine (Berlin, Germany), 2000-01, Vol.78 (5), p.282-286

2000

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In vivo angiogenesis in normal and portal hypertensive rats: role of basic fibroblast growth factor and nitric oxide

Journal of hepatology, 2001-05, Vol.34 (5), p.644-650

2001

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Radiosensitivity in Nijmegen Breakage Syndrome cells is attributable to a repair defect and not cell cycle checkpoint defects

Cancer research (Chicago, Ill.), 2000-09, Vol.60 (17), p.4881-4888

2000

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Increased angiogenesis in portal hypertensive rats: Role of nitric oxide

Hepatology (Baltimore, Md.), 1999-04, Vol.29 (4), p.1044-1049

1999

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Gain of androgen receptor gene copies in primary prostate cancer due to X chromosome polysomy

The Prostate, 2004-04, Vol.59 (1), p.59-68

2004

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A mixture model of nuchal translucency thickness in screening for chromosomal defects: validation of a single operator dataset

First-Trimester Prenatal Diagnosis of Okihiro Syndrome

Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probes

Impaired p53-mediated DNA damage response, cell-cycle disturbance and chromosome aberrations in Nijmegen breakage syndrome lymphoblastoid cell lines

High frequency of spontaneous translocations revealed by FISH in cells from patients with the cancer-prone syndromes ataxia telangiectasia and Nijmegen breakage syndrome

Multi-locus (ML)-FISH is a reliable tool for nondisjunction studies in human oocytes

STI571 Enhances the Therapeutic Index of Epothilone B by a Tumor-selective Increase of Drug Uptake

Improved definition of chromosomal breakpoints using high-resolution multicolour banding

Frequency of CFTR gene mutations in males participating in an ICSI programme

Heterozygous Submicroscopic Inversions Involving Olfactory Receptor–Gene Clusters Mediate the Recurrent t(4;8)(p16;p23) Translocation

Patupilone Induced Vascular Disruption in Orthotopic Rodent Tumor Models Detected by Magnetic Resonance Imaging and Interstitial Fluid Pressure

Increased cancer risk of heterozygotes with NBS1 germline mutations in poland

No evidence for a major role of heterozygous deletion 657del5 within the NBS1 gene in the pathogenesis of non‐Hodgkin's lymphoma of childhood and adolescence

Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnostics

Molecular characterization of the DICE1 (DDX26) tumor suppressor gene in lung carcinoma cells

High reliability and sensitivity of the BCR/ABL1 D-FISH test for the detection of BCR/ABL rearrangements

Attenuation of the formation of DNA-repair foci containing RAD51 in Fanconi anaemia

Molecular cytogenetic techniques for the diagnosis of chromosomal abnormalities in childhood disease

Mosaic tetrasomy 9p in a girl with multiple congenital anomalies : cytogenetic and molecular-cytogenetic studies

Radiosensitivity of Ataxia Telangiectasia and Nijmegen Breakage Syndrome Homozygotes and Heterozygotes as Determined by Three-Color FISH Chromosome Painting

Mutations of the gene encoding the transmembrane transporter protein ABC-C6 cause pseudoxanthoma elasticum

In vivo angiogenesis in normal and portal hypertensive rats: role of basic fibroblast growth factor and nitric oxide

Radiosensitivity in Nijmegen Breakage Syndrome cells is attributable to a repair defect and not cell cycle checkpoint defects

Increased angiogenesis in portal hypertensive rats: Role of nitric oxide

Gain of androgen receptor gene copies in primary prostate cancer due to X chromosome polysomy

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