Revisit on a distinctive chromosome 1p36 deletion syndrome: report of one case and review of the English literature

Review

Meng-Luen Lee et al. Int J Cardiol. 2004 Sep.

. 2004 Sep;96(3):477-80.

doi: 10.1016/j.ijcard.2003.04.072.

No abstract available

Similar articles

Terminal 2q37 deletion and autistic behaviour.
Lukusa T, Smeets E, Vogels A, Vermeesch JR, Fryns JP. Lukusa T, et al. Genet Couns. 2005;16(2):179-80. Genet Couns. 2005. PMID: 16080299 No abstract available.
Proximal interstitial 1p36 deletion syndrome: the most proximal 3.5-Mb microdeletion identified on a dysmorphic and mentally retarded patient with inv(3)(p14.1q26.2).
Shimojima K, Páez MT, Kurosawa K, Yamamoto T. Shimojima K, et al. Brain Dev. 2009 Sep;31(8):629-33. doi: 10.1016/j.braindev.2008.08.013. Epub 2008 Oct 5. Brain Dev. 2009. PMID: 18835671
Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
Battaglia A, Hoyme HE, Dallapiccola B, Zackai E, Hudgins L, McDonald-McGinn D, Bahi-Buisson N, Romano C, Williams CA, Brailey LL, Zuberi SM, Carey JC. Battaglia A, et al. Pediatrics. 2008 Feb;121(2):404-10. doi: 10.1542/peds.2007-0929. Pediatrics. 2008. PMID: 18245432
Maternal uniparental disomy chromosome 14: case report and literature review.
Falk MJ, Curtis CA, Bass NE, Zinn AB, Schwartz S. Falk MJ, et al. Pediatr Neurol. 2005 Feb;32(2):116-20. doi: 10.1016/j.pediatrneurol.2004.07.007. Pediatr Neurol. 2005. PMID: 15664772 Review.
Del 1p36 syndrome: a newly emerging clinical entity.
Battaglia A. Battaglia A. Brain Dev. 2005 Aug;27(5):358-61. doi: 10.1016/j.braindev.2004.03.011. Brain Dev. 2005. PMID: 16023552 Review.

Cardiovascular Phenotypic Spectrum of 1p36 Deletion Syndrome.
Kaur T, Sriram CS, Prasanna P, Kohli U. Kaur T, et al. J Pediatr Genet. 2021 Jul 29;12(4):329-334. doi: 10.1055/s-0041-1732473. eCollection 2023 Dec. J Pediatr Genet. 2021. PMID: 38162160 Free PMC article.