Deletion of PTEN and BMPR1A on Chromosome 10q23 Is Not Always Associated with Juvenile Polyposis of Infancy
- 1 September 2006
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 79 (3), 593-596
- https://doi.org/10.1086/507151
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Contiguous Gene Deletion within Chromosome Arm 10q Is Associated with Juvenile Polyposis of Infancy, Reflecting Cooperation between the BMPR1A and PTEN Tumor-Suppressor GenesAmerican Journal of Human Genetics, 2006
- Genetic conditions associated with intestinal juvenile polypsAmerican Journal Of Medical Genetics Part C-Seminars In Medical Genetics, 2004
- PTEN: One Gene, Many SyndromesHuman Mutation, 2003
- Spectrum of clinical variability in familial deletion 22q11.2: from full manifestation to extremely mild clinical anomaliesClinical Genetics, 2003
- DiGeorge syndrome: the use of model organisms to dissect complex geneticsHuman Molecular Genetics, 2002
- The molecular basis for apoptotic defects in patients with CD95 (Fas/Apo-1) mutationsJournal of Clinical Investigation, 1999
- Deletion 10q23.2-q23.33 in a patient with gastrointestinal juvenile polyposis and other features of a Cowden-like syndromeGenes, Chromosomes and Cancer, 1998
- Monozygotic twins with chromosome 22q11 deletion and discordant phenotype.Journal of Medical Genetics, 1995
- Juvenile polyposisBritish Journal of Surgery, 1995
- Hereditary polypoid diseases of the gastrointestinal tract: A working classificationThe American Journal of Surgery, 1975