Use of sanger and next-generation sequencing to screen for mosaic and intronic APC variants in unexplained colorectal polyposis patients.

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Title: Use of sanger and next-generation sequencing to screen for mosaic and intronic APC variants in unexplained colorectal polyposis patients.
Authors: Elsayed FA; Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands., Tops CMJ; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands., Nielsen M; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands., Morreau H; Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands., Hes FJ; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands., van Wezel T; Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands. T.van_Wezel@lumc.nl.
Source: Familial cancer [Fam Cancer] 2022 Jan; Vol. 21 (1), pp. 79-83. Date of Electronic Publication: 2021 Mar 08.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Springer Country of Publication: Netherlands NLM ID: 100898211 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-7292 (Electronic) Linking ISSN: 13899600 NLM ISO Abbreviation: Fam Cancer Subsets: MEDLINE
Database: MEDLINE Ultimate
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ISSN:1573-7292
DOI:10.1007/s10689-021-00236-2