Mucinous cystadenoma of ovary in a patient with juvenile polyposis due to 10q23 microdeletion: Expansion of phenotype
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference18 articles.
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3. Segmental overgrowth, lipomatosis, arteriovenous malformation and epidermal nevus (SOLAMEN) syndrome is related to mosaic PTEN nullizygosity;Caux;Eur J Hum Genet,2007
4. Contiguous gene deletion within chromosome arm 10q is associated with juvenile polyposis of infancy, reflecting cooperation between the BMPR1A and PTEN tumor-suppressor genes;Delnatte;Am J Hum Genet,2006
5. BMP signaling inhibits intestinal stem cell self-renewal through suppression of Wnt-beta-catenin signaling;He;Nat Genet,2004
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1. Early-Onset Ovarian Cancer <30 Years: What Do We Know about Its Genetic Predisposition?;International Journal of Molecular Sciences;2023-11-30
2. Proximal variants in CCND2 associated with microcephaly, short stature, and developmental delay: A case series and review of inverse brain growth phenotypes;American Journal of Medical Genetics Part A;2021-06-04
3. PTENHamartoma tumor syndrome in childhood: A review of the clinical literature;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2019-10-14
4. Looking for the hidden mutation: Bannayan–Riley–Ruvalcaba syndrome caused by constitutional and mosaic 10q23 microdeletions involving PTEN and BMPR1A;American Journal of Medical Genetics Part A;2019-05-06
5. Management of Juvenile Polyposis Syndrome in Children and Adolescents: A Position Paper From the ESPGHAN Polyposis Working Group;Journal of Pediatric Gastroenterology & Nutrition;2019-03
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