ASXL1 - Bohring-Opitz syndrome

This test is available for the following conditions:

  • Conditions > Multiple congenital anomalies (MCA) > Bohring-Opitz syndrome

This product is also part of the following panels:

  • Hereditary cancer panel
  • Inherited bone marrow failure and/or predisposition panel to hematological malignancies
  • Intellectual disability panel
  • Mendelian inherited disorders panel
  • Orofacial clefting panel
  • Primary immunodeficiencies panel
  • Short stature/skeletal dysplasia panel
  • Skin disorders panel¹

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

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 612990
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 476

Gene

ASXL1 - Bohring-Opitz syndrome

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 476

ASXL1 - Bohring-Opitz syndrome



€ 476