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Items: 1 to 20 of 76

1.

Familial co-occurrence of congenital heart defects follows distinct patterns.

Ellesøe SG, Workman CT, Bouvagnet P, Loffredo CA, McBride KL, Hinton RB, van Engelen K, Gertsen EC, Mulder BJM, Postma AV, Anderson RH, Hjortdal VE, Brunak S, Larsen LA.

Eur Heart J. 2018 Mar 21;39(12):1015-1022. doi: 10.1093/eurheartj/ehx314.

2.

[Incidence of congenital heart defects in the Czech Republic--current data].

Sípek A, Gregor V, Sípek A Jr, Hudáková J, Horácek J, Klaschka J, Skibová J, Langhammer P, Petrzílková L, Klímová B, Perinová B, Wiesnerová J.

Ceska Gynekol. 2010 May;75(3):221-42. Czech.

PMID:
20731304
3.

Recurrence of congenital heart defects among siblings-a nationwide study.

Brodwall K, Greve G, Leirgul E, Tell GS, Vollset SE, Øyen N.

Am J Med Genet A. 2017 Jun;173(6):1575-1585. doi: 10.1002/ajmg.a.38237. Epub 2017 Apr 19.

PMID:
28425218
4.

Recurrence of discordant congenital heart defects in families.

Oyen N, Poulsen G, Wohlfahrt J, Boyd HA, Jensen PK, Melbye M.

Circ Cardiovasc Genet. 2010 Apr;3(2):122-8. doi: 10.1161/CIRCGENETICS.109.890103. Epub 2010 Feb 20.

PMID:
20173214
5.

Familial recurrence of congenital heart disease in patients with ostium secundum atrial septal defect.

Caputo S, Capozzi G, Russo MG, Esposito T, Martina L, Cardaropoli D, Ricci C, Argiento P, Pacileo G, Calabrò R.

Eur Heart J. 2005 Oct;26(20):2179-84. Epub 2005 Jun 24.

PMID:
15980033
6.

Evaluation of prenatal diagnosis of associated congenital heart diseases by fetal ultrasonographic examination in Europe.

Stoll C, Garne E, Clementi M; EUROSCAN Study Group.

Prenat Diagn. 2001 Apr;21(4):243-52.

PMID:
11288111
7.

Influence of genes and the environment in familial congenital heart defects.

Wang X, Li P, Chen S, Xi L, Guo Y, Guo A, Sun K.

Mol Med Rep. 2014 Feb;9(2):695-700. doi: 10.3892/mmr.2013.1847. Epub 2013 Dec 6.

PMID:
24337398
8.

Noncardiac malformations in congenital heart disease: a retrospective analysis of 305 pediatric autopsies.

Güçer S, Ince T, Kale G, Akçören Z, Ozkutlu S, Talim B, Cağlar M.

Turk J Pediatr. 2005 Apr-Jun;47(2):159-66.

PMID:
16052857
9.

Risk of congenital heart disease in relatives of probands with conotruncal cardiac defects: an evaluation of 1,620 families.

Peyvandi S, Ingall E, Woyciechowski S, Garbarini J, Mitchell LE, Goldmuntz E.

Am J Med Genet A. 2014 Jun;164A(6):1490-5. doi: 10.1002/ajmg.a.36500. Epub 2014 Mar 26.

10.

Associated genetic syndromes and extracardiac malformations strongly influence outcomes of fetuses with congenital heart diseases.

Bensemlali M, Bajolle F, Ladouceur M, Fermont L, Lévy M, Le Bidois J, Salomon LJ, Bonnet D.

Arch Cardiovasc Dis. 2016 May;109(5):330-6. doi: 10.1016/j.acvd.2016.01.006. Epub 2016 Mar 25.

11.

Recurrence of congenital heart defects in families.

Øyen N, Poulsen G, Boyd HA, Wohlfahrt J, Jensen PK, Melbye M.

Circulation. 2009 Jul 28;120(4):295-301. doi: 10.1161/CIRCULATIONAHA.109.857987. Epub 2009 Jul 13.

PMID:
19597048
12.

[Fetal echocardiography and clinical genetics--a close correlation].

Zerres K, Gembruch U, Schwanitz G, Redel DA, Bald R, Gottschlich A, Hansmann M.

Z Kardiol. 1990 Feb;79(2):96-106. German.

PMID:
2321416
13.

Genome-wide linkage analysis of congenital heart defects using MOD score analysis identifies two novel loci.

Flaquer A, Baumbach C, Piñero E, García Algas F, de la Fuente Sanchez MA, Rosell J, Toquero J, Alonso-Pulpon L, Garcia-Pavia P, Strauch K, Heine-Suñer D.

BMC Genet. 2013 May 24;14:44. doi: 10.1186/1471-2156-14-44.

15.

Recent advances in the understanding of genetic causes of congenital heart defects.

Gelb BD.

Front Biosci. 2000 Mar 1;5:D321-33. Review.

PMID:
10704426
16.

Cardiovascular malformations caused by NOTCH1 mutations do not keep left: data on 428 probands with left-sided CHD and their families.

Kerstjens-Frederikse WS, van de Laar IM, Vos YJ, Verhagen JM, Berger RM, Lichtenbelt KD, Klein Wassink-Ruiter JS, van der Zwaag PA, du Marchie Sarvaas GJ, Bergman KA, Bilardo CM, Roos-Hesselink JW, Janssen JH, Frohn-Mulder IM, van Spaendonck-Zwarts KY, van Melle JP, Hofstra RM, Wessels MW.

Genet Med. 2016 Sep;18(9):914-23. doi: 10.1038/gim.2015.193. Epub 2016 Jan 28.

PMID:
26820064
17.

Familial recurrence of nonsyndromic congenital heart defects in first degree relatives of patients with deletion 22q11.2.

Digilio MC, Marino B, Capolino R, Angioni A, Sarkozy A, Roberti MC, Conti E, de Zorzi A, Dallapiccola B.

Am J Med Genet A. 2005 Apr 15;134A(2):158-64.

PMID:
15669097
18.

Familial recurrence of congenital heart disease: an overview and review of the literature.

Calcagni G, Digilio MC, Sarkozy A, Dallapiccola B, Marino B.

Eur J Pediatr. 2007 Feb;166(2):111-6. Epub 2006 Nov 8. Review.

PMID:
17091259
19.

Familial recurrence of heart defects in subjects with congenitally corrected transposition of the great arteries.

Piacentini G, Digilio MC, Capolino R, Zorzi AD, Toscano A, Sarkozy A, D'Agostino R, Marasini M, Russo MG, Dallapiccola B, Marino B.

Am J Med Genet A. 2005 Aug 30;137(2):176-80.

PMID:
16059940
20.

Recurrence of congenital heart disease in cases with familial risk screened prenatally by echocardiography.

Fesslova V, Brankovic J, Lalatta F, Villa L, Meli V, Piazza L, Ricci C.

J Pregnancy. 2011;2011:368067. doi: 10.1155/2011/368067. Epub 2011 Oct 1.

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