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Mutation analysis of the NRXN1 gene in autism spectrum disorders.
Balkan J Med Genet. 2017 Mar 8;19(2):17-22. doi: 10.1515/bjmg-2016-0031. eCollection 2016 Dec 1.
Balkan J Med Genet. 2017.
PMID: 28289584
Free PMC article.
Familial Prenatal Total Anomalous Pulmonary Venous Drainage: Genetic Implications and Multimodal Echocardiographic and MRI Assessment.
Granozio G, Velasco Forte MN, Egloff A, Woodgate T, Low KJ, Kavasoglu AN, Bellsham-Revell H, Pushparajah K, Vazquez-Garcia L, Lloyd DFA.
Granozio G, et al. Among authors: kavasoglu an.
JACC Case Rep. 2025 Aug 6;30(22):104551. doi: 10.1016/j.jaccas.2025.104551.
JACC Case Rep. 2025.
PMID: 40780769
Free PMC article.
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Identifying the Impacts, Obstacles and Information Barriers for Parents of Children Living With Genetic Neurodevelopmental Disorders: A Qualitative Study.
Low KJ; GenROC Consortium; Treneman-Evans G, Wynn SL, Ingram J.
Low KJ, et al.
Health Expect. 2025 Aug;28(4):e70340. doi: 10.1111/hex.70340.
Health Expect. 2025.
PMID: 40607502
Free PMC article.
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