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USP6 gene rearrangement in nodular fasciitis and histological mimics

Histopathology, 2016-11, Vol.69 (5), p.784-791

2016

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NRASQ61R Mutation-specific Immunohistochemistry Also Identifies the HRASQ61R Mutation in Medullary Thyroid Cancer and May Have a Role in Triaging Genetic Testing for MEN2

The American journal of surgical pathology, 2017-01, Vol.41 (1), p.75-81

2017

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NRASQ61R Mutation-specific Immunohistochemistry is Highly Specific for Either NRAS Q61R or KRAS Q61R Mutation in Colorectal Carcinoma

Applied immunohistochemistry & molecular morphology, 2017-08, Vol.25 (7), p.475-480

2017

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FISH Detection of PML-RARA Fusion in ins(15;17) Acute Promyelocytic Leukaemia Depends on Probe Size

BioMed research international, 2013-01, Vol.2013 (2013), p.1-4

2013

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NRASQ61R Mutation-specific Immunohistochemistry is Highly Specific for Either NRASQ61R or KRASQ61R Mutation in Colorectal Carcinoma

Applied immunohistochemistry & molecular morphology, 2017-08, Vol.25 (7), p.475

2017

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Cytogenetic changes in metastatic renal cell carcinoma: Basis for sensitivity and resistance to everolimus

Journal of clinical oncology, 2012-05, Vol.30 (15_suppl), p.e15050-e15050

2012

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53. USP6 gene rearrangement in nodular fasciitis

Pathology, 2015, Vol.47, p.S116-S116

2015

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Cytogenetic changes in renal cell carcinoma: Basis for sensitivity and resistance to everolimus

Journal of clinical oncology, 2012-02, Vol.30 (5_suppl), p.403-403

2012

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Dovitinib in first-line metastatic renal cell carcinoma and correlation of efficacy with tumor gene status: A phase II clinical trial

Journal of clinical oncology, 2014-05, Vol.32 (15_suppl), p.4569-4569

2014

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Dovitinib in first-line renal cell carcinoma: An investigation into tumour gene status and correlation with efficacy: A phase II clinical trial

Journal of clinical oncology, 2014-02, Vol.32 (4_suppl), p.443-443

2014

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Aids-related plasmablastic lymphoma of the oral cavity associated with an IgH/MYC translocation treatment with autologous stem-cell transplantation in a patient with severe haemophilia-A

Haematologica (Roma), 2007-01, Vol.92 (1), p.e11-e12

2007

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Enduring Response to Everolimus as Third-Line Therapy in a Patient With Advanced Renal Cell Carcinoma, Including Small-Bowel Metastases: Loss of FHIT but Normal VHL Gene Status

Clinical genitourinary cancer, 2012-09, Vol.10 (3), p.202-206

2012

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Differentiation between malignant melanoma and Spitz tumour has improved over the past decade due to modern pathological techniques

New Zealand medical journal, 2013-08, Vol.126 (1381), p.87-91

Ng, Daniel

2013

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IgE-type multiple myeloma with the late development of IgA2 kappa and plasma cell leukaemia

Pathology, 2010-01, Vol.42 (1), p.82-84

2010

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Analysis of Molecular Cytogenetic Changes in Metastatic Renal Cell Carcinoma in the Setting of Everolimus Treatment: A Pilot Project

Clinical genitourinary cancer, 2014-08, Vol.12 (4), p.256-261

2014

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Epiphyseal dysplasia and other skeletal anomalies in a patient with the 6p25 microdeletion syndrome

American journal of medical genetics. Part A, 2006-09, Vol.140A (18), p.1955-1959

2006

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Cervical intraepithelial neoplasia and aneusomy of TERC: Assessment of liquid-based cytological preparations

Diagnostic cytopathology, 2009-06, Vol.37 (6), p.411-415

2009

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The Utility of Peripheral Blood FISH in the Quantitation of BCR/ABL in CML Patients on Imatinib Mesylate: A Comparison with Bone Marrow FISH and Conventional Cytogenetics

Blood, 2004-11, Vol.104 (11), p.2942-2942

2004

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Another case of interstitial del(12) involving the proposed cardio-facio-cutaneous candidate region

American journal of medical genetics. Part A, 2005-07, Vol.136A (1), p.12-16

2005

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Partial tetrasomy 15 due to a unique inverted triplication of chromosome15q24-q26

American journal of medical genetics. Part A, 2004-10, Vol.130A (2), p.208-210

2004

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Dermatofibrosarcoma protuberans: report of a case with a variant ring chromosome and metastases following pregnancy

Journal of cutaneous pathology, 2006-05, Vol.33 (5), p.383-388

2006

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Fusion of Platelet-Derived Growth Factor β to a Novel Gene KIAA1509 on Chromosome 14 in an Atypical Myeloproliferative Disorder Associated with Eosinophilia

Blood, 2004-11, Vol.104 (11), p.2437-2437

2004

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False-positive diagnosis of trisomy 21 using fluorescence in situ hybridisation (FISH) on uncultured amniotic fluid cells

Prenatal diagnosis, 2003-04, Vol.23 (4), p.302-305

2003

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Homozygous deletion of SHOX in a mentally retarded male with Langer mesomelic dysplasia

Journal of medical genetics, 2000-12, Vol.37 (12), p.959-964

2000

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Severe musculoskeletal phenotype associated with an unbalanced t(6;10) translocation: Clarification of the locus for this phenotype on distal 6p

American journal of medical genetics, 2003-06, Vol.119A (3), p.288-292

2003

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USP6 gene rearrangement in nodular fasciitis and histological mimics

NRASQ61R Mutation-specific Immunohistochemistry Also Identifies the HRASQ61R Mutation in Medullary Thyroid Cancer and May Have a Role in Triaging Genetic Testing for MEN2

NRASQ61R Mutation-specific Immunohistochemistry is Highly Specific for Either NRAS Q61R or KRAS Q61R Mutation in Colorectal Carcinoma

FISH Detection of PML-RARA Fusion in ins(15;17) Acute Promyelocytic Leukaemia Depends on Probe Size

NRASQ61R Mutation-specific Immunohistochemistry is Highly Specific for Either NRASQ61R or KRASQ61R Mutation in Colorectal Carcinoma

Cytogenetic changes in metastatic renal cell carcinoma: Basis for sensitivity and resistance to everolimus

53. USP6 gene rearrangement in nodular fasciitis

Cytogenetic changes in renal cell carcinoma: Basis for sensitivity and resistance to everolimus

Dovitinib in first-line metastatic renal cell carcinoma and correlation of efficacy with tumor gene status: A phase II clinical trial

Dovitinib in first-line renal cell carcinoma: An investigation into tumour gene status and correlation with efficacy: A phase II clinical trial

Aids-related plasmablastic lymphoma of the oral cavity associated with an IgH/MYC translocation treatment with autologous stem-cell transplantation in a patient with severe haemophilia-A

Enduring Response to Everolimus as Third-Line Therapy in a Patient With Advanced Renal Cell Carcinoma, Including Small-Bowel Metastases: Loss of FHIT but Normal VHL Gene Status

Differentiation between malignant melanoma and Spitz tumour has improved over the past decade due to modern pathological techniques

IgE-type multiple myeloma with the late development of IgA2 kappa and plasma cell leukaemia

Analysis of Molecular Cytogenetic Changes in Metastatic Renal Cell Carcinoma in the Setting of Everolimus Treatment: A Pilot Project

Epiphyseal dysplasia and other skeletal anomalies in a patient with the 6p25 microdeletion syndrome

Cervical intraepithelial neoplasia and aneusomy of TERC: Assessment of liquid-based cytological preparations

The Utility of Peripheral Blood FISH in the Quantitation of BCR/ABL in CML Patients on Imatinib Mesylate: A Comparison with Bone Marrow FISH and Conventional Cytogenetics

Another case of interstitial del(12) involving the proposed cardio-facio-cutaneous candidate region

Partial tetrasomy 15 due to a unique inverted triplication of chromosome15q24-q26

Dermatofibrosarcoma protuberans: report of a case with a variant ring chromosome and metastases following pregnancy

Fusion of Platelet-Derived Growth Factor β to a Novel Gene KIAA1509 on Chromosome 14 in an Atypical Myeloproliferative Disorder Associated with Eosinophilia

False-positive diagnosis of trisomy 21 using fluorescence in situ hybridisation (FISH) on uncultured amniotic fluid cells

Homozygous deletion of SHOX in a mentally retarded male with Langer mesomelic dysplasia

Severe musculoskeletal phenotype associated with an unbalanced t(6;10) translocation: Clarification of the locus for this phenotype on distal 6p

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