Overgrowth of prenatal onset associated with submicroscopic 9q22.3 deletion
- PMID: 21412971
- DOI: 10.1002/ajmg.a.33835
Overgrowth of prenatal onset associated with submicroscopic 9q22.3 deletion
Similar articles
-
Perinatal findings and molecular cytogenetic analyses of de novo interstitial deletion of 9q (9q22.3-->q31.3) associated with Gorlin syndrome.Prenat Diagn. 2006 Aug;26(8):725-9. doi: 10.1002/pd.1496. Prenat Diagn. 2006. PMID: 16927391
-
Clinical features of microdeletion 9q22.3 (pat).Clin Genet. 2009 Apr;75(4):384-93. doi: 10.1111/j.1399-0004.2008.01141.x. Clin Genet. 2009. PMID: 19320658
-
Wilms' tumor in patients with 9q22.3 microdeletion syndrome suggests a role for PTCH1 in nephroblastomas.Eur J Hum Genet. 2013 Jul;21(7):784-7. doi: 10.1038/ejhg.2012.252. Epub 2012 Nov 21. Eur J Hum Genet. 2013. PMID: 23169491 Free PMC article.
-
[The PATCHED/Sonic Hedgehog signalling pathway in superficial bladder cancer].Med Sci (Paris). 2003 Oct;19(10):920-5. doi: 10.1051/medsci/20031910920. Med Sci (Paris). 2003. PMID: 14613000 Review. French.
-
Interstitial deletion 9q22.32-q33.2 associated with additional familial translocation t(9;17)(q34.11;p11.2) in a patient with Gorlin-Goltz syndrome and features of Nail-Patella syndrome.Am J Med Genet A. 2004 Jan 15;124A(2):179-91. doi: 10.1002/ajmg.a.20367. Am J Med Genet A. 2004. PMID: 14699618 Review.
Cited by
-
9q22 Deletion--first familial case.Orphanet J Rare Dis. 2011 Jun 22;6:45. doi: 10.1186/1750-1172-6-45. Orphanet J Rare Dis. 2011. PMID: 21693067 Free PMC article.
-
A Clinical Review of Generalized Overgrowth Syndromes in the Era of Massively Parallel Sequencing.Mol Syndromol. 2018 Feb;9(2):70-82. doi: 10.1159/000484532. Epub 2018 Jan 25. Mol Syndromol. 2018. PMID: 29593474 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical