FGF9

OMIMHGNC

Locus: 13q12.11

Protein: Fibroblast growth factor 9

 

Disorders

Tests

Test Type
Molecular (5)
Multi-Gene Panel (3)
Multi-Method Panel (2)
Test Method
Del/Dup (CNV) (1)
Mutation Scanning of Entire Coding Region (1)
Sequencing, Capillary (Sanger) (2)
Sequencing, Next Gen (4)
Prenatal/Carrier
Carrier (1)
Lab Location
Spain(3)
USA(1)
Germany(1)
 
TAT: 7-8 weeks
price: contact lab
NGS of 6 genes: FGF9, FLNB, GDF5, HOXA11, NOG, TTR.
method(s): ◦ Mutation Scanning of Entire Coding Region ◦ Sequencing, Next Gen 
Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain
Multiple Synostosis Syndrome Type 3 , Sequencing FGF9 Gene
method(s): ◦ Sequencing, Capillary (Sanger) 
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain
TAT: 4-6 weeks
price: contact lab
Selected Genetic Syndromes with skeletal involvement Panel
method(s): ◦ Sequencing, Next Gen 
CeGaT GmbH - Tübingen, Germany
Multiple Synostosis Syndrome and Related Disorders, Panel Massive Sequencing (NGS) 6 Genes
method(s): ◦ Sequencing, Next Gen 
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain
TAT: 4-5 Weeks
price: contact lab
FGF9
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Fulgent Diagnostics - Temple City, CA, USA