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8. High burden of genetic conditions diagnosed in a cardiac neurodevelopmental clinic. Goldenberg PC; Adler BJ; Parrott A; Anixt J; Mason K; Phillips J; Cooper DS; Ware SM; Marino BS Cardiol Young; 2017 Apr; 27(3):459-466. PubMed ID: 27641144 [TBL] [Abstract][Full Text] [Related]
9. Neurodevelopmental delay with critical congenital heart disease is mainly from prenatal injury not infant cardiac surgery: current evidence based on a meta-analysis of functional magnetic resonance imaging. Li Y; Yin S; Fang J; Hua Y; Wang C; Mu D; Zhou K Ultrasound Obstet Gynecol; 2015 Jun; 45(6):639-48. PubMed ID: 24913334 [TBL] [Abstract][Full Text] [Related]
10. Diagnostic genetic testing for neurodevelopmental psychiatric disorders: closing the gap between recommendation and clinical implementation. Finucane BM; Ledbetter DH; Vorstman JA Curr Opin Genet Dev; 2021 Jun; 68():1-8. PubMed ID: 33434711 [TBL] [Abstract][Full Text] [Related]
13. Congenital Heart Disease and Neurodevelopment: Clinical Manifestations, Genetics, Mechanisms, and Implications. Nattel SN; Adrianzen L; Kessler EC; Andelfinger G; Dehaes M; Côté-Corriveau G; Trelles MP Can J Cardiol; 2017 Dec; 33(12):1543-1555. PubMed ID: 29173597 [TBL] [Abstract][Full Text] [Related]
14. Genetic counselling and testing in adults with congenital heart disease: A consensus document of the ESC Working Group of Grown-Up Congenital Heart Disease, the ESC Working Group on Aorta and Peripheral Vascular Disease and the European Society of Human Genetics. De Backer J; Bondue A; Budts W; Evangelista A; Gallego P; Jondeau G; Loeys B; Peña ML; Teixido-Tura G; van de Laar I; Verstraeten A; Roos Hesselink J Eur J Prev Cardiol; 2020 Sep; 27(13):1423-1435. PubMed ID: 31184212 [TBL] [Abstract][Full Text] [Related]
15. Improving Neurodevelopmental Surveillance and Follow-up in Infants with Congenital Heart Disease. Michael M; Scharf R; Letzkus L; Vergales J Congenit Heart Dis; 2016; 11(2):183-8. PubMed ID: 26899508 [TBL] [Abstract][Full Text] [Related]
16. [Heart abnormalities and genetic counseling]. Lambotte C; Richelle C Rev Med Liege; 1979 Jun; 34(12):560-75. PubMed ID: 379951 [No Abstract] [Full Text] [Related]
17. Recurrent copy number variations as risk factors for neurodevelopmental disorders: critical overview and analysis of clinical implications. Torres F; Barbosa M; Maciel P J Med Genet; 2016 Feb; 53(2):73-90. PubMed ID: 26502893 [TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of susceptibility loci for neurodevelopmental disorders - genetic counseling and pregnancy outcome in 57 cases. Govaerts L; Srebniak M; Diderich K; Joosten M; Riedijk S; Knapen M; Go A; Papatsonis D; de Graaf K; Toolenaar T; van der Steen S; Huijbregts G; Knijnenburg J; de Vries F; Van Opstal D; Galjaard RJ Prenat Diagn; 2017 Jan; 37(1):73-80. PubMed ID: 27931090 [TBL] [Abstract][Full Text] [Related]
20. [Eugenic counseling after a birth of an infant with congenital malformations]. Beolchini PE Minerva Med; 1972 Nov; 63(85):4660-4. PubMed ID: 4264406 [No Abstract] [Full Text] [Related] [Next] [New Search]