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FGFR1 - Hartsfield syndrome

This test is available for the following conditions:

Conditions > Multiple congenital anomalies (MCA) > Hartsfield syndrome
Conditions > Skeletal > Hartsfield syndrome

This product is also part of the following panels:

panel craniosynostosis (FGFR1 (ex7), FGFR2, GFR3 (ex6), TWIST1) ¹

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

Sequence analysis of all coding exons and flanking intron-exon boundaries
Deletion/duplication analysis (MLPA)

OMIM: 136350
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

GEN

complete analysis

targeted analysis of a familial mutation

€ 723

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Hartsfield syndrome

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Gene

FGFR1 - Hartsfield syndrome

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Performing laboratory
Radboudumc

€ 723

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FGFR1 - Hartsfield syndrome

GEN

complete analysis

targeted analysis of a familial mutation

€ 723

Add Update Remove

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