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Low concentrations of STI571 in the cerebrospinal fluid: a case report

British journal of haematology, 2002-06, Vol.117 (3), p.623-625

2002

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Germline mutation of the E-cadherin gene in three sibling cases with advanced gastric cancer: clinical consequences for the other family members

European journal of gastroenterology & hepatology, 2010-03, Vol.22 (3), p.306-310

2010

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Counting the repetitive kringle-IV repeats in the gene encoding human apolipoprotein(a) by fibre-FISH

Nature genetics, 1999-04, Vol.21 (4), p.357-358

1999

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Mental and psychomotoric retardation in two brothers with pure partial trisomy 7q32-q34 due to a maternal insertion (14;7)

American journal of medical genetics, 2000-04, Vol.91 (4), p.291-297

2000

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Evidence from a leukaemia model for maintenance of vascular endothelium by bone-marrow-derived endothelial cells

The Lancet (British edition), 2000-05, Vol.355 (9216), p.1688-1691

2000

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Autosomal dominant frontometaphyseal dysplasia: Delineation of the clinical phenotype

American journal of medical genetics. Part A, 2017-07, Vol.173 (7), p.1739-1746

2017

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Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal Dysplasia

American journal of human genetics, 2016-08, Vol.99 (2), p.392-406

2016

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Combination of Cytology, Fluorescence In Situ Hybridization for Aneuploidy, and Reverse-Transcriptase Polymerase Chain Reaction for Human Mammaglobin/Mammaglobin B Expression Improves Diagnosis of Malignant Effusions

Journal of clinical oncology, 2004-02, Vol.22 (3), p.474-483

2004

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Mapping of balanced chromosome translocation breakpoints to the basepair level from microdissected chromosomes

Journal of cellular and molecular medicine, 2010-08, Vol.14 (8), p.2078-2084

2010

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High rate of molecular alteration in histologically tumour-free bronchial epithelium of NSCLC patients detected by multicolour fluorescence in situ hybridisation

Oncology reports, 2006-05, Vol.15 (5), p.1233-1240

2006

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Fluorescence in situ hybridization (FISH) on peripheral blood smears for monitoring Philadelphia chromosome-positive chronic myeloid leukemia (CML) during interferon treatment: A new strategy for remission assessment

Genes chromosomes & cancer, 1998-02, Vol.21 (2), p.90-100

1998

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Automated real-time PCR to determine K-ras codon 12 mutations in non-small cell lung cancer: comparison with immunohistochemistry and clinico-pathological features

International journal of oncology, 2003-10, Vol.23 (4), p.1121

2003

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Circulating endothelial cells after transplantation

The Lancet (British edition), 2001-05, Vol.357 (9266), p.1449-1449

2001

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Contribution of Endothelial Cells of Hematopoietic Origin to Blood Vessel Formation

Circulation research, 2001-01, Vol.88 (1), p.e1-e1

2001

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FISH cytogenetics and prognosis in breast and non–small cell lung cancers

Cytometry. Part B, Clinical cytometry, 2004-11, Vol.62B (1), p.52-56

2004

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Characterisation and predictive value of epidermal growth factor receptor status using quantitative real-time PCR combined with immunohistochemistry on non-small cell lung cancer specimens

International journal of oncology, 2003-10, Vol.23 (4), p.893

2003

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Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations : delineation of the phenotype

Human genetics, 1997-05, Vol.99 (5), p.596-601

1997

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Muellerian aplasia associated with ring chromosome 8p12q12 mosaicism

American journal of medical genetics. Part A, 2003-01, Vol.116A (3), p.290-294

2003

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The elastin gene is disrupted in a family with a balanced translocation t(7;16)(q11.23;q13) associated with a variable expression of the Williams-Beuren syndrome

European journal of human genetics : EJHG, 2002-06, Vol.10 (6), p.351-361

2002

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Improving tumor cell detection in pleural effusions by interphase cytogenetics

Cytometry. Part B, Clinical cytometry, 2003-09, Vol.55B (1), p.60-62

2003

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Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome

Journal of medical genetics, 1997-04, Vol.34 (4), p.309-313

1997

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Comparison of automated cellular imaging system and manual microscopy for immunohistochemically stained cryostat sections of lung cancer specimens applying p53, ki-67 and p120

Oncology reports, 2003-01, Vol.10 (1), p.15

2003

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An excess of chromosome 1 breakpoints in male infertility

European journal of human genetics : EJHG, 2004-12, Vol.12 (12), p.993-1000

2004

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Characterisation of a collecting duct carcinoma by cytogenetic analysis and comparative genomic hybridisation

International journal of oncology, 1998-09, Vol.13 (3), p.461

1998

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High-resolution mapping of the human 4q21 and the mouse 5E3 SCYB chemokine cluster by fiber-fluorescence in situ hybridization

Immunogenetics (New York), 2001-09, Vol.53 (7), p.611-615

2001

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Low concentrations of STI571 in the cerebrospinal fluid: a case report

Germline mutation of the E-cadherin gene in three sibling cases with advanced gastric cancer: clinical consequences for the other family members

Counting the repetitive kringle-IV repeats in the gene encoding human apolipoprotein(a) by fibre-FISH

Mental and psychomotoric retardation in two brothers with pure partial trisomy 7q32-q34 due to a maternal insertion (14;7)

Evidence from a leukaemia model for maintenance of vascular endothelium by bone-marrow-derived endothelial cells

Autosomal dominant frontometaphyseal dysplasia: Delineation of the clinical phenotype

Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal Dysplasia

Combination of Cytology, Fluorescence In Situ Hybridization for Aneuploidy, and Reverse-Transcriptase Polymerase Chain Reaction for Human Mammaglobin/Mammaglobin B Expression Improves Diagnosis of Malignant Effusions

Mapping of balanced chromosome translocation breakpoints to the basepair level from microdissected chromosomes

High rate of molecular alteration in histologically tumour-free bronchial epithelium of NSCLC patients detected by multicolour fluorescence in situ hybridisation

Fluorescence in situ hybridization (FISH) on peripheral blood smears for monitoring Philadelphia chromosome-positive chronic myeloid leukemia (CML) during interferon treatment: A new strategy for remission assessment

Automated real-time PCR to determine K-ras codon 12 mutations in non-small cell lung cancer: comparison with immunohistochemistry and clinico-pathological features

Circulating endothelial cells after transplantation

Contribution of Endothelial Cells of Hematopoietic Origin to Blood Vessel Formation

FISH cytogenetics and prognosis in breast and non–small cell lung cancers

Characterisation and predictive value of epidermal growth factor receptor status using quantitative real-time PCR combined with immunohistochemistry on non-small cell lung cancer specimens

Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations : delineation of the phenotype

Muellerian aplasia associated with ring chromosome 8p12q12 mosaicism

The elastin gene is disrupted in a family with a balanced translocation t(7;16)(q11.23;q13) associated with a variable expression of the Williams-Beuren syndrome

Improving tumor cell detection in pleural effusions by interphase cytogenetics

Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome

Comparison of automated cellular imaging system and manual microscopy for immunohistochemically stained cryostat sections of lung cancer specimens applying p53, ki-67 and p120

An excess of chromosome 1 breakpoints in male infertility

Characterisation of a collecting duct carcinoma by cytogenetic analysis and comparative genomic hybridisation

High-resolution mapping of the human 4q21 and the mouse 5E3 SCYB chemokine cluster by fiber-fluorescence in situ hybridization

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