WNT10A

Wingless-type MMTV integration site family, member 10A
80326

 

Schopf-Schulz-Passarge syndrome – 224750

Tooth agenesis, selective, 4 – 150400

Ectodermal dysplasia 16 (odontoonychodermal dysplasia) – 257980

 

DNA onderzoek is hier aan te vragen:

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