CGC Genetics - Absence of ulna and fibula, with severe limb deficiency | Fuhrmann syndrome (deletion/duplication analysis of WNT7A gene)

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Absence of ulna and fibula, with severe limb deficiency | Fuhrmann syndrome (deletion/duplication analysis of WNT7A gene)

WNT7A

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Turnaround Time (Days)

- 60

Specialties

- Dermatology, Rare diseases, Pediatrics, Dysmorphology

CGC Reference

- 4562

Associated Tests

Ulna and fibula, absence of, with severe limb deficiency (sequence analysis of WNT7A gene)