Congenital anomalies of kidney and urinary tract (CAKUT) Multi-Gene Panels method(s): ◦ Sequencing, Next Gen Center for Human Genetics and Laboratory Medicine Martinsried, Molecular Genetics - Martinsried, Germany |
Lymphedema-Distichiasis Syndrome , Sequencing FOXC2 Gene method(s): ◦ Sequencing, Capillary (Sanger) Reference Laboratory Genetics - Hospitalet de Llobregat, Spain |
Lymphedema-distichiasis syndrome (sequence analysis of FOXC2 gene) method(s): ◦ Sequencing, Capillary (Sanger) CGC Genetics - Porto, Portugal |
TAT: 4-8 weeks price: $635.00
Analysis FOXC2 gene (Lymphedema-Distichiasis Syndrome) method(s): ◦ Sequencing, Capillary (Sanger) Academic Medical Centre, University of Amsterdam, DNA Diagnostics Laboratory - Amsterdam, Netherlands |
NGS Non-immune Hydrops Panel method(s): ◦ Sequencing, Next Gen Greenwood Genetic Center Diagnostic Laboratories - Greenwood, SC, USA |
Lymphedema Distichiasis method(s): ◦ Sequencing, Capillary (Sanger) South West Thames Genetics Laboratory, St George's University of London - London, United Kingdom |
Lymphedema-Lethal Restrictive Dermopathy, Panel Massive Sequencing (NGS) 9 Genes method(s): ◦ Sequencing, Next Gen Reference Laboratory Genetics - Hospitalet de Llobregat, Spain |
Vascular and lymphatic disorders Panel method(s): ◦ Sequencing, Next Gen CeGaT GmbH - Tübingen, Germany |
TAT: 11-13 weeks price: $1,880.00
Analysis Lymphedema Genes (NGS panel 36 genes) method(s): ◦ Sequencing, Next Gen Academic Medical Centre, University of Amsterdam, DNA Diagnostics Laboratory - Amsterdam, Netherlands |
FOXC2 method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) Fulgent Diagnostics - Temple City, CA, USA |
Lymphedema-distichiasis Syndrome: FOXC2 gene method(s): ◦ Sequencing, Capillary (Sanger) GenoMed-Diagnosticos de Medicina Molecular, SA - Lisboa, Portugal |
TAT: 3-4 weeks price: $690.00
Lymphedema-Distichiasis Syndrome via the FOXC2 Gene method(s): ◦ Del/Dup (CNV) PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
TAT: 3-4 weeks price: $840.00
Lymphedema Deletion/Duplication Panel method(s): ◦ Del/Dup (CNV) PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
TAT: 2-3 weeks price: $560.00
Lymphedema-Distichiasis Syndrome via the FOXC2 Gene method(s): ◦ Sequencing, Capillary (Sanger) PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
TAT: 3-5 weeks price: $1,940.00
Lymphedema Sequencing Panel method(s): ◦ Sequencing, Next Gen PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
Lymphedema-distichiasis syndrome method(s): ◦ Sequencing, Capillary (Sanger) Centogene AG, Rare Disease Company - Rostock, Germany |
Anterior Segment Dysgenesis method(s): ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen Molecular Vision Laboratory - Portland, OR, USA |
NGS Vascular Disorders Panel method(s): ◦ Sequencing, Next Gen Greenwood Genetic Center Diagnostic Laboratories - Greenwood, SC, USA |
Renal Malformation Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, Helsinki - Helsinki, Finland |
Renal Malformation Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, San Francisco - San Francisco, CA, USA |