Genetics in medicine Genetics in Medicine, 24(10), 2112-2122. Lippincott Williams and Wilkins Genetics in Medicine, 24, 2112-2122 Genetics in Medicine, 24(10), 2112-2122. Nature Publishing Group Genetics in Medicine, 24(10), 2112-2122. ELSEVIER SCIENCE INC Genetics in Medicine, 24(10), 2112-2122. Lippincott Williams & Wilkins Genetics in Medicine, 24, 10, pp. 2112-2122 van den Bersselaar, L M, Verhagen, J M A, Bekkers, J A, Kempers, M, Houweling, A C, Baars, M, Overwater, E, Hilhorst-Hofstee, Y, Barge-Schaapveld, D Q C M, Rompen, E, Krapels, I P C, Dulfer, E, Wessels, M W, Loeys, B L, Verhagen, H J M, Maugeri, A, Roos-Hesselink, J W, Brüggenwirth, H T & van de Laar, I M B H 2022, ' Expanding the genetic and phenotypic spectrum of ACTA2-related vasculopathies in a Dutch cohort ', Genetics in Medicine, vol. 24, no. 10, pp. 2112-2122 . https://doi.org/10.1016/j.gim.2022.07.009 Genetics in medicine, 24(10), 2112-2122. Lippincott Williams and Wilkins
Circulation. Genomic and Precision Medicine, 16, 1 Circulation: Genomic and Precision Medicine, 16(1):E003672. LIPPINCOTT WILLIAMS & WILKINS Circulation. Genomic and precision medicine, 16(1). Lippincott Williams and Wilkins Ltd. Circulation: Genomic and Precision Medicine, 16(1), 69-79. Lippincott Williams and Wilkins Ltd. Circulation. Genomic and Precision Medicine, 16 Circulation: Genomic and Precision Medicine, 16(1). Lippincott Williams & Wilkins
Circulation. Genomic and Precision Medicine, 15, 5, pp. 375-385 van der Meulen, M H, Herkert, J C, den Boer, S L, du Marchie Sarvaas, G J, Blom, N A, ten Harkel, A D J, Breur, H M P J, Rammeloo, L A J, Tanke, R B, Marcelis, C, van de Laar, I M B H, Verhagen, J M A, Lekanne Dit Deprez, R H, Barge-Schaapveld, D Q C M, Baas, A F, Sammani, A, Christiaans, I, van Tintelen, J P & Dalinghaus, M 2022, ' Genetic Evaluation of A Nation-Wide Dutch Pediatric DCM Cohort : The Use of Genetic Testing in Risk Stratification ', Circulation: Genomic and Precision Medicine, vol. 15, no. 5, pp. 375-385 . https://doi.org/10.1161/CIRCGEN.120.002981 Circulation. Genomic and precision medicine, 15(5), 375-385. Lippincott Williams and Wilkins Ltd. Circulation. Genomic and precision medicine, 15(5), 375-385. Lippincott Williams & Wilkins Circulation. Genomic and precision medicine, 15(5):e002981. LIPPINCOTT WILLIAMS & WILKINS Circulation: Genomic and Precision Medicine, 15(5), 375-385. Lippincott Williams and Wilkins Ltd. Circulation. Genomic and Precision Medicine, 15, 375-385 Circulation: Genomic and Precision Medicine, 15(5), 375-385. LIPPINCOTT WILLIAMS & WILKINS
Genetics in Medicine Genetics in medicine, 23(11), 2122-2137. Lippincott Williams and Wilkins Genetics in Medicine, 23(11), 2122-2137. SPRINGERNATURE Genetics in Medicine, 23(11), 2122-2137. Nature Publishing Group Genomics England Research Consortium 2021, ' Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome ', Genetics in Medicine, vol. 23, no. 11, pp. 2122-2137 . https://doi.org/10.1038/s41436-021-01246-2 Genetics in Medicine, 23(11), 2122-2137. Lippincott Williams and Wilkins Genetics in Medicine, 23(11), 2122-2137. Lippincott Williams & Wilkins Genetics in Medicine, 23, 2122-2137 Genetics in Medicine, 23, 11, pp. 2122-2137 Genomics England Research Consortium 2021, ' Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome ', Genetics in medicine : official journal of the American College of Medical Genetics . https://doi.org/10.1038/s41436-021-01246-2
Am J Hum Genet American Journal of Human Genetics, 108, 1692-1709 Stolz, J R, Foote, K M, Veenstra-Knol, H E, Pfundt, R, ten Broeke, S W, de Leeuw, N, Roht, L, Pajusalu, S, Part, R, Rebane, I, Õunap, K, Stark, Z, Kirk, E P, Lawson, J A, Lunke, S, Christodoulou, J, Louie, R J, Rogers, R C, Davis, J M, Innes, A M, Wei, X C, Keren, B, Mignot, C, Lebel, R R, Sperber, S M, Sakonju, A, Dosa, N, Barge-Schaapveld, D Q C M, Peeters-Scholte, C M P C D, Ruivenkamp, C A L, van Bon, B W, Kennedy, J, Low, K J, Ellard, S, Pang, L, Junewick, J J, Mark, P R, Carvill, G L & Swanson, G T 2021, ' Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders ', American Journal of Human Genetics, vol. 108, no. 9, pp. 1692-1709 . https://doi.org/10.1016/j.ajhg.2021.07.007 American Journal of Human Genetics, 108(9), 1692-1709. CELL PRESS American Journal of Human Genetics, 108, 9, pp. 1692-1709
Cells, 10(11). MDPI Multidisciplinary Digital Publishing Institute Cells Cells, 10(11):2950. Multidisciplinary Digital Publishing Institute (MDPI) Cells, Vol 10, Iss 2950, p 2950 (2021) Cells, 10(11):2950. MDPI Multidisciplinary Digital Publishing Institute Schuldt, M, van Driel, B, Algül, S, Parbhudayal, R Y, Barge-Schaapveld, D Q C M, Güçlü, A, Jansen, M, Michels, M, Baas, A F, van de Wiel, M A, Nieuwdorp, M, Levin, E, Germans, T, Jans, J J M & van der Velden, J 2021, ' Distinct Metabolomic Signatures in Preclinical and Obstructive Hypertrophic Cardiomyopathy ', Cells, vol. 10, no. 11 . https://doi.org/10.3390/cells10112950 Cells, 10(11). MDPI Cells; Volume 10; Issue 11; Pages: 2950