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Clinical phenotype of FOXP1 syndrome: Parent-reported medical signs and symptoms in 40 individuals

Document Type

Article

Author

Koene, S.; Santen, G.W.E.; Ropers, F.G.; Berghuis, D.; Wieland, J.; Rybak, T.; Wildschut, F.; Morgan, A.; Trelles, M.P.; Scheepe, J.R.; Bökenkamp, R.; Peeters-Scholte, C.M.P.C.D.; Braden, R.

Source

In: Journal of Medical Genetics. (Journal of Medical Genetics, 2023)

Subject

Language

English

ISSN

14686244
00222593

Online Access

Full Text (BMJ Journals) Full Text (ProQuest Central) Web of Science JCR 저널정보 Scopus Find it@PNU

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