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Patients with 10q22.3q23.1 recurrent deletion syndrome are at risk for juvenile polyposis

Document Type

Article

Author

Lecoquierre, F.; Cassinari, K.; Chambon, P.; Nicolas, G.; Frebourg, T.; Houdayer, C.; Baert-Desurmont, S.; Malsa, S.; Marlin, R.; Bera, O.; Assouline, Y.; Fléjou, J.-F.

Source

In: European Journal of Medical Genetics. (European Journal of Medical Genetics, April 2020, 63(4))

Subject

Language

English

ISSN

18780849
17697212

Online Access

Full Text (ScienceDirect 종량제) Full Text (Clinical Key) Web of Science JCR 저널정보 Scopus Find it@PNU

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