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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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2 Maximum shipping time to ensure sample quality

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)