Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome

C. Tziotzios, G. Petrof, L. Liu, A. Verma, E. K. Wedgeworth, J. E. Mellerio, J. A. McGrath*

*Corresponding author for this work

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28 Citations (Scopus)

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Medicine and Dentistry

Biochemistry, Genetics and Molecular Biology