Citations for
1BMPR1A, DEL10Q23
Juvenile polyposis and other intestinal polyposis syndromes with microdeletions of chromosome 10q22-23.
Dahdaleh F, Carr J, Calva D, Howe J.
Clin Genet 81(2):110-116. doi: 10.1111/j.1399-0004.2011.01763.x. Epub 2011 Sep 6. 2012
2BMPR1A, DEL10Q22, DEL10Q23, DUP10Q23, GRID1, NRG3
The phenotype of recurrent 10q22q23 deletions and duplications.
van Bon BW, Balciuniene J, Fruhman G, Nagamani SC, Broome DL, Cameron E, Martinet D, Roulet E, Jacquemont S, Beckmann JS, Irons M, Potocki L, Lee B, Cheung SW, Patel A, Bellini M, Selicorni A, Ciccone R, Silengo M, Vetro A, Knoers NV, de Leeuw N, Pfundt R, Wolf B, Jira P, Aradhya S, Stankiewicz P, Brunner HG, Zuffardi O, Selleck SB, Lupski JR, de Vries BB.
Eur J Hum Genet 19(4):400-8. Epub 2011 Jan 19. 2011
3BMPR1A, DEL10Q22, DEL10Q23
Clinical and molecular characterization of individuals with recurrent genomic disorder at 10q22.3q23.2.
Alliman S, Coppinger J, Marcadier J, Thiese H, Brock P, Shafer S, Weaver C, Asamoah A, Leppig K, Dyack S, Morash B, Schultz R, Torchia BS, Lamb AN, Bejjani BA.
Clin Genet lin Genet. 2010 Feb 9. [Epub ahead of print]PMID: 20345475 2010
4BMPR1A, DEL10Q23, PTEN
Mucinous cystadenoma of ovary in a patient with juvenile polyposis due to 10q23 microdeletion: Expansion of phenotype.
Babovic N, Simmons PS, Moir C, Thorland EC, Scheithauer B, Gliem TJ, Babovic-Vuksanovic D.
Am J Med Genet A 152A(10):2623-7.PMID: 20815035 2010
5BMPRA, DEL10Q23
Clinical and molecular characterization of individuals with recurrent genomic disorder at 10q22.3q23.2.
Alliman S, Coppinger J, Marcadier J, Thiese H, Brock P, Shafer S, Weaver C, Asamoah A, Leppig K, Dyack S, Morash B, Schultz R, Torchia BS, Lamb AN, Bejjani BA.
Clin Genet 78(2):162-8. Epub 2010 Feb 9. 2010
6DEL10Q23, PTEN, BMPRA
Variable phenotypes associated with 10q23 microdeletions involving the PTEN and BMPR1A genes.
Menko FH, Kneepkens CM, de Leeuw N, Peeters EA, Van Maldergem L, Kamsteeg EJ, Davidson R, Rozendaal L, Lasham CA, Peeters-Scholte CM, Jansweijer MC, Hilhorst-Hofstee Y, Gille JJ, Heins YM, Nieuwint AW, Sistermans EA.
Clin Genet 74(2):145-54. Epub 2008 May 28. 2008
7DEL10Q23, DEL10Q22
Recurrent 10q22-q23 Deletions: A Genomic Disorder on 10q Associated with Cognitive and Behavioral Abnormalities.
Balciuniene J, Feng N, Iyadurai K, Hirsch B, Charnas L, Bill BR, Easterday MC, Staaf J, Oseth L, Czapansky-Beilman D, Avramopoulos D, Thomas GH, Borg A, Valle D, Schimmenti LA, Selleck SB.
Am J Hum Genet 80(5):938-47. Epub 2007 Mar 20. 2007
8DEL10Q23, BMPR1A, PTEN, JPS2
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 C, Sanlaville D, Mougenot JF, Vermeesch JR, Houdayer C, Blois MC, Genevieve D, Goulet O, Fryns JP, Jaubert F, Vekemans M, Lyonnet S, Romana S, Eng C, Stoppa-Lyonnet D.
Am J Hum Genet 78(6):1066-74. Epub 2006 Apr 14. 2006
9DEL10Q23
Deletion of PTEN and BMPR1A on chromosome 10q23 is not always associated with juvenile polyposis of infancy.
Salviati L, Patricelli M, Guariso G, Sturniolo GC, Alaggio R, Bernardi F, Zuffardi O, Tenconi R.
Am J Hum Genet 79(3):593-6; author reply 596-7. No abstract available. 2006
10DEL10Q23, JPS, PTEN, PTEN, TSG10A
Deletion 10q23.2-q23.33 in a patient with gastrointestinal juvenile polyposis and other features of a Cowden-like syndrome.
Tsuchiya KD, Wiesner G, Cassidy SB, Limwongse C, Boyle JT, Schwartz S.
Genes Chromosomes Cancer 21(2):113-8. 1998