Case Reports
Occurrence of 19p- in an infant with multiple dysmorphic features
- PMID: 6609675
Item in Clipboard
Case Reports
Occurrence of 19p- in an infant with multiple dysmorphic features
Ann Genet.
1984.
Abstract
A case with partial deletion on the short arm of one chromosome 19 and multiple dysmorphic features is reported.
Similar articles
-
Partial deletion of the short arm of chromosome 12(p11; p13). Report of a case.Ann Genet. 1975 Jun;18(2):95-8. Ann Genet. 1975. PMID: 1081371
-
Stillborn baby with partial monosomy of the short arm of chromosome 5 and partial trisomy of the short arm of chromosome 20.Congenit Anom (Kyoto). 2005 Dec;45(4):161-4. doi: 10.1111/j.1741-4520.2005.00087.x. Congenit Anom (Kyoto). 2005. PMID: 16359498
-
[Interstitial deletion of the long arm of chromosome 7 in a female child with leprechaunism].Ann Genet. 1976 Dec;19(4):265-8. Ann Genet. 1976. PMID: 797303 French.
-
A new case of interstitial deletion of chromosome 3q, del(3q)(q13.12q21.3), with agenesis of the corpus callosum.Clin Dysmorphol. 1994 Oct;3(4):292-6. Clin Dysmorphol. 1994. PMID: 7894733 Review.
-
Terminal deletion of the long arm of chromosome 3 [46,XX,del(3)(q27-->qter)].Am J Med Genet. 1996 Jan 2;61(1):45-8. doi: 10.1002/(SICI)1096-8628(19960102)61:1<45::AID-AJMG9>3.0.CO;2-W. Am J Med Genet. 1996. PMID: 8741917 Review.
Cited by
-
Perinatal findings in a patient with a novel large chromosome 19p deletion.Clin Case Rep. 2018 Jun 21;6(8):1525-1530. doi: 10.1002/ccr3.1615. eCollection 2018 Aug. Clin Case Rep. 2018. PMID: 30147897 Free PMC article.
-
A novel chromosome 19p13.12 deletion in a child with multiple congenital anomalies.Am J Med Genet A. 2009 Mar;149A(3):396-402. doi: 10.1002/ajmg.a.32691. Am J Med Genet A. 2009. PMID: 19215039 Free PMC article.
-
Telomeres: a diagnosis at the end of the chromosomes.J Med Genet. 2003 Jun;40(6):385-98. doi: 10.1136/jmg.40.6.385. J Med Genet. 2003. PMID: 12807958 Free PMC article. Review.
-
Ocular Manifestations of a Novel Proximal 19p13.3 Microdeletion.Case Rep Genet. 2018 Apr 30;2018:2492437. doi: 10.1155/2018/2492437. eCollection 2018. Case Rep Genet. 2018. PMID: 29854496 Free PMC article.
-
Chromosome 19p13.3 deletion in a child with Peutz-Jeghers syndrome, congenital heart defect, high myopia, learning difficulties and dysmorphic features: Clinical and molecular characterization of a new contiguous gene syndrome.Genet Mol Biol. 2011 Oct;34(4):557-61. doi: 10.1590/S1415-47572011005000044. Epub 2011 Oct 1. Genet Mol Biol. 2011. PMID: 22215957 Free PMC article.