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Journal of Medical Genetics|September 4, 2023
Biallelic truncating variants in <i>VGLL2</i> cause syngnathia in humansValeria Agostini, Aude Tessier, Nabila Djaziri, et al.Molecular Genetics & Genomic Medicine|February 6, 2014
Mutations in the interleukin receptor IL11RA cause autosomal recessive Crouzon-like craniosynostosisKatharina Keupp, Yun Li, Ibrahim Vargel, et al.Pageof 2