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Multiplex PCR: Critical Parameters and Step-by-Step Protocol

BioTechniques, 1997-09, Vol.23 (3), p.504-511

1997

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Phenotypic variability in trisomy 13 mosaicism: Two new patients and literature review

American journal of medical genetics. Part A, 2009-06, Vol.149A (6), p.1346-1358

2009

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Update on Late Relapse of Germ Cell Tumor: A Clinical and Molecular Analysis

Journal of clinical oncology, 2003-01, Vol.21 (1), p.113-122

2003

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Acute panmyelosis with myelofibrosis: an entity distinct from acute megakaryoblastic leukemia

Modern pathology, 2005-05, Vol.18 (5), p.603-614

2005

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Chronic lymphocytic leukemia/small lymphocytic lymphoma with trisomy 12 and focal cyclin d1 expression: a potential diagnostic pitfall

Archives of pathology & laboratory medicine (1976), 2005-01, Vol.129 (1), p.92-95

2005

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Variable phenotype of familial adenomatous polyposis in pedigrees with 3′ mutation in the APC gene

Gut, 1998-10, Vol.43 (4), p.548-552

1998

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Characterization of Neo-Centromeres in Marker Chromosomes Lacking Detectable Alpha-satellite DNA

Human molecular genetics, 1997-08, Vol.6 (8), p.1195-1204

1997

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49,XXXXY: a distinct phenotype. Three new cases and review

Journal of medical genetics, 1998-05, Vol.35 (5), p.420-424

1998

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Validation of Scales to Measure Benefits of and Barriers to Colorectal Cancer Screening

Journal of psychosocial oncology, 2001-01, Vol.19 (3-4), p.47-63

2001

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AML1-FOG2 fusion protein in myelodysplasia

Blood, 2005-06, Vol.105 (11), p.4523-4526

2005

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Clinical outcome and follow‐up of the first reported case of Russell‐Silver syndrome with the unique combination of maternal uniparental heterodisomy 7 and mosaic trisomy 7

Birth defects research. A Clinical and molecular teratology, 2005-08, Vol.73 (8), p.577-582

2005

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A report of three patients with an interstitial deletion of chromosome 15q24

American journal of medical genetics. Part A, 2005-08, Vol.137A (1), p.65-71

2005

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HER-2/neu expression in germ cell tumours

Journal of clinical pathology, 2002-09, Vol.55 (9), p.656-658

2002

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Genetic diagnosis of PLP gene duplications/deletions in patients with Pelizaeus-Merzbacher disease

Clinical genetics, 2005-11, Vol.68 (5), p.466-467

2005

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Small Marker Chromosome Identification in Metaphase and Interphase Using Centromeric Multiplex FISH (CM-FISH)

Laboratory investigation, 2001-04, Vol.81 (4), p.475-481

2001

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Partial trisomy 2q: Report of a patient with dup (2)(q33.1q35)

American journal of medical genetics. Part A, 2005-04, Vol.134A (1), p.80-83

2005

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Large cell carcinoma of the lung mimicking a germ cell tumor: The potential value of chromosome analysis

Lung cancer (Amsterdam, Netherlands), 2005-08, Vol.49 (2), p.271-274

2005

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Cryptic Translocation Identification in Human and Mouse Using Several Telomeric Multiplex FISH (TM-FISH) Strategies

Laboratory investigation, 2001-04, Vol.81 (4), p.483-491

2001

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Turner Syndrome (45x) with Clitoromegaly

The Journal of urology, 2003-10, Vol.170 (4), p.1355-1356

2003

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Cytogenetic analysis and construction of a BAC contig across a common neocentromeric region from 9p

Chromosoma, 2001-08, Vol.110 (4), p.275-283

2001

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Triple-color FISH analysis of 12p amplification in testicular germ-cell tumors using 12p band-specific painting probes

Journal of molecular medicine (Berlin, Germany), 1998-08, Vol.76 (9), p.648-655

1998

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Acute graft-versus-host disease of the lung after liver transplantation

Liver transplantation, 2002-10, Vol.8 (10), p.968-971, Article ajlts0080968

2002

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Evaluating current policy for detecting mosaicism in amniotic fluid cultures: implications for current cell counting practices

Statistics in medicine, 2005-02, Vol.24 (4), p.615-622

2005

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Proficiency testing for laboratories performing fluorescence in situ hybridization with chromosome-specific DNA probes

Archives of pathology & laboratory medicine (1976), 2002-12, Vol.126 (12), p.1458-1462

2002

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As currently formulated, ISCN FISH nomenclature make it not practical for use in clinical test reports or cytogenetic databases

Genetics in medicine, 2003-09, Vol.5 (5), p.370-377

2003

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Multiplex PCR: Critical Parameters and Step-by-Step Protocol

Phenotypic variability in trisomy 13 mosaicism: Two new patients and literature review

Update on Late Relapse of Germ Cell Tumor: A Clinical and Molecular Analysis

Acute panmyelosis with myelofibrosis: an entity distinct from acute megakaryoblastic leukemia

Chronic lymphocytic leukemia/small lymphocytic lymphoma with trisomy 12 and focal cyclin d1 expression: a potential diagnostic pitfall

Variable phenotype of familial adenomatous polyposis in pedigrees with 3′ mutation in the APC gene

Characterization of Neo-Centromeres in Marker Chromosomes Lacking Detectable Alpha-satellite DNA

49,XXXXY: a distinct phenotype. Three new cases and review

Validation of Scales to Measure Benefits of and Barriers to Colorectal Cancer Screening

AML1-FOG2 fusion protein in myelodysplasia

Clinical outcome and follow‐up of the first reported case of Russell‐Silver syndrome with the unique combination of maternal uniparental heterodisomy 7 and mosaic trisomy 7

A report of three patients with an interstitial deletion of chromosome 15q24

HER-2/neu expression in germ cell tumours

Genetic diagnosis of PLP gene duplications/deletions in patients with Pelizaeus-Merzbacher disease

Small Marker Chromosome Identification in Metaphase and Interphase Using Centromeric Multiplex FISH (CM-FISH)

Partial trisomy 2q: Report of a patient with dup (2)(q33.1q35)

Large cell carcinoma of the lung mimicking a germ cell tumor: The potential value of chromosome analysis

Cryptic Translocation Identification in Human and Mouse Using Several Telomeric Multiplex FISH (TM-FISH) Strategies

Turner Syndrome (45x) with Clitoromegaly

Cytogenetic analysis and construction of a BAC contig across a common neocentromeric region from 9p

Triple-color FISH analysis of 12p amplification in testicular germ-cell tumors using 12p band-specific painting probes

Acute graft-versus-host disease of the lung after liver transplantation

Evaluating current policy for detecting mosaicism in amniotic fluid cultures: implications for current cell counting practices

Proficiency testing for laboratories performing fluorescence in situ hybridization with chromosome-specific DNA probes

As currently formulated, ISCN FISH nomenclature make it not practical for use in clinical test reports or cytogenetic databases

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