Concepedia

Publication | Open Access

Oto-facial syndrome and esophageal atresia, intellectual disability and zygomatic anomalies - expanding the phenotypes associated with EFTUD2 mutations

DOIFull Paper Access

54

Citations

14

References

2013

Year

Claudia Voigt, André Mégarbané, Kornelia Neveling, Johanna Christina Czeschik, Beate Albrecht, Bert Callewaert, Florian von Deimling, Andreas Hehr, Marie Falkenberg Smeland, Rainer König,
Orphanet Journal of Rare Diseases

References

YearCitations

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