Perinatal findings in a patient with a novel large chromosome 19p deletion-Reference-Cited by-同舟云学术

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Perinatal findings in a patient with a novel large chromosome 19p deletion

Published:2018-06-21 Issue:8 Volume:6 Page:1525-1530
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

Culjat Marko¹^ORCID,Razak Jennifer²,Saadeh-Haddad Reem³,Driggers Rita²⁴,Kamholz Karen¹,Timofeev Julia²⁴

Affiliation:

1. MedStar Georgetown University Hospital; Neonatal-Perinatal Medicine; Washington DC USA

2. Division of Maternal Fetal Medicine; Sibley Memorial Hospital; Washington DC USA

3. Department of Pediatrics; MedStar Georgetown University Hospital; Washington DC USA

4. Division of Maternal Fetal Medicine; Johns Hopkins School of Medicine; Baltimore MD USA

Publisher

Wiley

Subject

General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ccr3.1615/fullpdf

Reference21 articles.

1. Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3-pter;Archer;Am J Med Genet A,2005

2. Split hand-foot malformation, tetralogy of Fallot, mental retardation and a 1 Mb 19p deletion-evidence for further heterogeneity?;Aten;Am J Med Genet A,2009

3. Array-CGH detection of a de novo 0.7-Mb deletion in 19p13.13 including CACNA1A associated with mental retardation and epilepsy with infantile spasms;Auvin;Epilepsia,2009

4. Genotype-phenotype relationship in three cases with overlapping 19p13.12 microdeletions;Bonaglia;Eur J Hum Genet,2010

5. Occurrence of 19p- in an infant with multiple dysmorphic features;Hurgoiu;Ann Genet,1984

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