Feingold Syndrome 1 Test
method(s): ◦ Sequencing, Capillary (Sanger)
Exeter Molecular Genetics, Royal Devon & Exeter Hospital - Exeter, United Kingdom |
Feingold (ODED) Syndrome Test (the MYCN gene-entire)
method(s): ◦ Sequencing, Capillary (Sanger)
GENESIS Center for Medical Genetics, Laboratory of Molecular Genetics - Poznan, Poland |
Feingold Syndrome 1 Test
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV)
Alfred I. duPont Hospital for Children, Molecular Diagnostics Lab - Wilmington, DE, USA |
Skeletal Dysplasia: Sequencing Panel
method(s):
Emory University School of Medicine, Emory Molecular Genetics Laboratory - Atlanta, GA, USA |
Limb Malformation: Sequencing Panel
method(s):
Emory University School of Medicine, Emory Molecular Genetics Laboratory - Atlanta, GA, USA |
Neurology: Sequencing Panel
method(s):
Emory University School of Medicine, Emory Molecular Genetics Laboratory - Atlanta, GA, USA |
Facial Dysostosis Sequencing Panel
method(s): ◦ Sequencing, Next Gen
University of Chicago, Genetic Services Laboratory - Chicago, IL, USA |
MYCN Del/Dup
method(s): ◦ Del/Dup (CNV)
GeneDx - Gaithersburg, MD, USA |
MYCN Gene Sequencing
method(s): ◦ Sequencing, Capillary (Sanger)
GeneDx - Gaithersburg, MD, USA |
Microcephaly Panel
method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen
GeneDx - Gaithersburg, MD, USA |
Feingold Syndrome, Sequencing MYCN Gene
method(s): ◦ Sequencing, Capillary (Sanger)
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain |
Feingold syndrome (sequence analysis of MYCN gene)
method(s): ◦ Sequencing, Capillary (Sanger)
CGC Genetics - Porto, Portugal |
Feingold Syndrome 1 Test
method(s): ◦ Sequencing, Capillary (Sanger)
Burc Molecular Genetics Laboratory - Istanbul, Turkey |
Facial Dysostosis Deletion/Duplication panel
method(s): ◦ Del/Dup (CNV)
University of Chicago, Genetic Services Laboratory - Chicago, IL, USA |
NewbornDx
method(s): ◦ Sequencing, Next Gen
Parabase Genomics - Boston, MA, USA |
Somatic Tumor Panel
method(s): ◦ Sequencing, Next Gen
CeGaT GmbH - Tübingen, Germany |
Single gene testing MYCN
method(s): ◦ Sequencing, Capillary (Sanger)
CeGaT GmbH - Tübingen, Germany |
Limb Malformation: Sequencing Panel
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen
CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada |
Limb Malformation: Deletion/Duplication Panel
method(s): ◦ Del/Dup (CNV)
CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada |
Skeletal Dysplasia: Sequencing Panel
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen
CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada |
Skeletal Dysplasia: Deletion/Duplication Panel
method(s): ◦ Del/Dup (CNV)
CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada |
Neurology: Sequencing Panel
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen
CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada |
Neurology: Deletion/Duplication Panel
method(s): ◦ Del/Dup (CNV)
CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada |
Intellectual Disability NGS Panel
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV)
Fulgent Diagnostics - Temple City, CA, USA |
MYCN
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV)
Fulgent Diagnostics - Temple City, CA, USA |
Skeletal Dysplasias NGS Panel
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV)
Fulgent Diagnostics - Temple City, CA, USA |
Facial Dysostosis Related Disorders, Panel Massive Sequencing (NGS) 10 Genes
method(s): ◦ Sequencing, Next Gen
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain |
Feingold syndrome
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV)
Centogene AG, Rare Disease Company - Rostock, Germany |
CentoICU Platinum
method(s): ◦ Sequencing, Next Gen
Centogene AG, Rare Disease Company - Rostock, Germany |
