Papers: 10.3390/genes12060875

https://doi.org/10.3390/genes12060875

The Diagnostic Journey of a Patient with Prader–Willi-Like Syndrome and a Unique Homozygous SNURF-SNRPN Variant; Bio-Molecular Analysis and Review of the Literature

Cited by: 3
Author(s): Karlijn Pellikaan, Geeske M. van Woerden, Lotte Kleinendorst, Anna G W Rosenberg, Bernhard Horsthemke, Christian Großer, Laura J. C. M. van Zutven, Elisabeth F C van Rossum, Aart-Jan van der Lely, James L. Resnick, Hennie T. Brüggenwirth, Mieke M. van Haelst, Laura C. G. de Graaff
Published: over 5 years ago

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