TAT: 4-8 weeks
price: $635.00
Beckwith-Wiedemann Syndrome (Methylation Test)
method(s): ◦ Methylation Analysis
Academic Medical Centre, University of Amsterdam, DNA Diagnostics Laboratory - Amsterdam, Netherlands |
TAT: 4-8 weeks
price: $330.00
Beckwith-Wiedemann Syndrome (UPD Test)
method(s): ◦ Uniparental Disomy
Academic Medical Centre, University of Amsterdam, DNA Diagnostics Laboratory - Amsterdam, Netherlands |
TAT: 2-3 weeks
price: $330.00
Beckwith-Wiedemann Syndrome (Deletion/Duplication Test)
method(s): ◦ Del/Dup (CNV)
Academic Medical Centre, University of Amsterdam, DNA Diagnostics Laboratory - Amsterdam, Netherlands |
TAT: 4-8 weeks
price: $635.00
Chromosome 11p15.5-Related Russell-Silver Syndrome Test
method(s): ◦ Methylation Analysis
Academic Medical Centre, University of Amsterdam, DNA Diagnostics Laboratory - Amsterdam, Netherlands |
Beckwith-Wiedemann Syndrome Test
method(s): ◦ Methylation Analysis
Genetics and Molecular Pathology - Melbourne, Australia |
Beckwith-Wiedemann Syndrome Test
method(s): ◦ Del/Dup (CNV)
University of Pennsylvania School of Medicine, Genetic Diagnostic Laboratory - Philadelphia, PA, USA |
Beckwith Wiedemann syndrome test
method(s): ◦ Methylation Analysis
Medical Genetics Center, Asan Medical Center - Seoul, Korea, Republic of |
Russell Silver syndrome test
method(s): ◦ Methylation Analysis
Medical Genetics Center, Asan Medical Center - Seoul, Korea, Republic of |
FISH-Beckwith-Wiedemann Syndrome
method(s): ◦ FISH-Metaphase
Baylor Miraca Genetics Laboratories - Houston, TX, USA |
Beckwith Wiedemann 11p15 Hypomethylation Analysis
method(s): ◦ Methylation Analysis
Biyolojik Bilimler Arastirma Gelistirme ve Uretim AS, Duzen Laboratuvarlar Grubu - Istanbul, Turkey |
Beckwith-Wiedemann Syndrome: H19 and LIT1 Methylation Panel
method(s):
Emory University School of Medicine, Emory Molecular Genetics Laboratory - Atlanta, GA, USA |
Russell-Silver Syndrome: H19 Methylation and UPD7 Panel
method(s):
Emory University School of Medicine, Emory Molecular Genetics Laboratory - Atlanta, GA, USA |
Russell-Silver Syndrome: H19 Methylation
method(s):
Emory University School of Medicine, Emory Molecular Genetics Laboratory - Atlanta, GA, USA |
Beckwith-Wiedemann Syndrome: H19 Methylation
method(s):
Emory University School of Medicine, Emory Molecular Genetics Laboratory - Atlanta, GA, USA |
Beckwith-Wiedemann Syndrome
method(s): ◦ Methylation Analysis ◦ Del/Dup (CNV) ◦ Uniparental Disomy
Hospital for Sick Children, Genome Diagnostics Laboratory (formerly Molecular Genetics Laboratory) - Toronto, Canada |
Russell-Silver Syndrome
method(s): ◦ Methylation Analysis ◦ Del/Dup (CNV)
Hospital for Sick Children, Genome Diagnostics Laboratory (formerly Molecular Genetics Laboratory) - Toronto, Canada |
Isolated hemihyperplasia (methylation analysis of KCNQ1OT1 and H19 genes)
method(s): ◦ Del/Dup (CNV) ◦ Genotyping (Microarray, Beads, etc.) ◦ Methylation Analysis
CGC Genetics - Porto, Portugal |
Russell-Silver Syndrome
method(s): ◦ Methylation Analysis
Burc Molecular Genetics Laboratory - Istanbul, Turkey |
Beckwith Wiedemann Syndrome
method(s): ◦ Del/Dup (CNV) ◦ Methylation Analysis
South West Thames Genetics Laboratory, St George's University of London - London, United Kingdom |
Hemihypertrophy
method(s): ◦ Methylation Analysis
South West Thames Genetics Laboratory, St George's University of London - London, United Kingdom |
Russell Silver Syndrome
method(s): ◦ Methylation Analysis
South West Thames Genetics Laboratory, St George's University of London - London, United Kingdom |
Wilms Tumour
method(s): ◦ Methylation Analysis
South West Thames Genetics Laboratory, St George's University of London - London, United Kingdom |
Beckwith-Wiedemann Syndrome Test
method(s): ◦ Del/Dup (CNV) ◦ Methylation Analysis
InterGenetics - Diagnostic Genetic Center - Athens, Greece |
Beckwith-Wiedemann Syndrome Test
method(s): ◦ Del/Dup (CNV) ◦ Methylation Analysis ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen ◦ Uniparental Disomy
MGZ München, Medizinisch Genetisches Zentrum München - München, Germany |
Chromosome 11p15.5-Related Russell-Silver Syndrome Test
method(s): ◦ Del/Dup (CNV) ◦ Methylation Analysis ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen ◦ Uniparental Disomy
MGZ München, Medizinisch Genetisches Zentrum München - München, Germany |
Russell-Silver Syndrome
method(s): ◦ Del/Dup (CNV) ◦ Methylation Analysis ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen ◦ Uniparental Disomy
MGZ München, Medizinisch Genetisches Zentrum München - München, Germany |
NewbornDx
method(s): ◦ Sequencing, Next Gen
Parabase Genomics - Boston, MA, USA |
Silver-Russel syndrome (deletion/duplication analysis of 11p15 and methylation analysis of DMR1 (H19) and DMR2 (KCNQ1OT1) regions)
method(s): ◦ Methylation Analysis ◦ Del/Dup (CNV)
CGC Genetics - Porto, Portugal |
Russell-Silver Syndrome: H19 Methylation
method(s): ◦ Methylation Analysis
CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada |
Russell-Silver Syndrome: H19 Methylation and UPD7 Panel
method(s): ◦ Methylation Analysis ◦ Uniparental Disomy
CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada |
Macrocephaly and Overgrowth Syndromes: Sequencing and Beckwith-Wiedemann Syndrome Methylation Panel
method(s): ◦ Methylation Analysis ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen
CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada |
Beckwith-Wiedemann Syndrome: H19 and LIT1 Methylation Panel
method(s): ◦ Methylation Analysis
CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada |
Beckwith-Wiedemann Syndrome: H19 Methylation
method(s): ◦ Methylation Analysis
CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada |
H19
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV)
Fulgent Diagnostics - Temple City, CA, USA |
Beckwith-Wiedemann Syndrome, Panel Massive Sequencing (NGS) 4 Genes
method(s): ◦ Sequencing, Next Gen
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain |
Beckwith-Wiedemann syndrome (Beckwith-Wiedemann-Syndrom)
method(s): ◦ Sequencing, Next Gen
Praxis fuer Humangenetik Wien - Vienna, Austria |
Beckwith-Wiedemann syndrome
method(s): ◦ Sequencing, Capillary (Sanger)
Centogene AG, Rare Disease Company - Rostock, Germany |
