RIN2 - marocephaly, alopecia, cutis laxa and scoliosis

This test is available for the following conditions:

  • Conditions > Intellectual Disability > MACS (Macrocefalic alopecia cutis laxa scoliosis)
  • Conditions > Multiple congenital anomalies (MCA) > MACS (Macrocefalic alopecia cutis laxa scoliosis)

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • 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: 610222
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane



€ 418
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Gene

RIN2 - marocephaly, alopecia, cutis laxa and scoliosis

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 418
View Add

RIN2 - marocephaly, alopecia, cutis laxa and scoliosis


€ 418
Add