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Shprintzen - Goldberg syndrome without intellectual disability: A clinical report and review of literature.

Autor: Chatelain C; Human Genetics Department, University Hospital of Liège, Avenue de l'Hôpital 1, 4000, Liège, Belgium. Electronic address: camille.chatelain@chuliege.be., Kukor L; Human Genetics Department, University Hospital of Liège, Avenue de l'Hôpital 1, 4000, Liège, Belgium., Bailleux S; Dermatology Department, University Hospital of Liège, Avenue de l'Hôpital 1, 4000, Liège, Belgium., Bours V; Human Genetics Department, University Hospital of Liège, Avenue de l'Hôpital 1, 4000, Liège, Belgium., Bulk S; Human Genetics Department, University Hospital of Liège, Avenue de l'Hôpital 1, 4000, Liège, Belgium., Docampo E; Human Genetics Department, University Hospital of Liège, Avenue de l'Hôpital 1, 4000, Liège, Belgium.

Publikováno v: European journal of medical genetics [Eur J Med Genet] 2024 Dec 03; Vol. 73, pp. 104985. Date of Electronic Publication: 2024 Dec 03.