Neonatal Screening

Displaying 1 - 4 of 4CSV
Kay, D. M., Sadeghi, H., Kier, C., Berdella, M., DeCelie‐Germana, J. K., Soultan, Z. N., Goetz, D. M., Caggana, M., Fortner, C. N., Giusti, R., Kaslovsky, R., Stevens, C., Voter, K., Welter, J. J., & Langfelder‐Schwind, E. (2024). Genetic counseling access and service delivery in New York State is variable for parents of infants with complex CFTR genotypes conferring uncertain phenotypes. Pediatric Pulmonology, 59(7), 1952–1961. Portico. https://doi.org/10.1002/ppul.27023
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Chang, S., Zhan, X., Liu, Y., Song, H., Gong, Z., Han, L., Maegawa, G. H. B., Gu, X., & Zhang, H. (2024). Newborn Screening for 6 Lysosomal Storage Disorders in China. JAMA Network Open, 7(5), e2410754. https://doi.org/10.1001/jamanetworkopen.2024.10754
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Green, N. S., Zapfel, A., Nnodu, O. E., Franklin, P., Tubman, V. N., Chirande, L., Kiyaga, C., Chunda-Liyoka, C., Awuonda, B., Ohene-Frempong, K., Inusa, B. P. D., Ware, R. E., Odame, I., Ambrose, E. E., Dogara, L. G., Oron, A. P., Willett, C., Thompson, A. A., Berliner, N., … Novelli, E. M. (2022). The Consortium on Newborn Screening in Africa for sickle cell disease: study rationale and methodology. Blood Advances, 6(24), 6187–6197. https://doi.org/10.1182/bloodadvances.2022007698
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Chung, W. K., Berg, J. S., Botkin, J. R., Brenner, S. E., Brosco, J. P., Brothers, K. B., Currier, R. J., Gaviglio, A., Kowtoniuk, W. E., Olson, C., Lloyd‐Puryear, M., Saarinen, A., Sahin, M., Shen, Y., Sherr, E. H., Watson, M. S., & Hu, Z. (2022). Newborn screening for neurodevelopmental diseases: Are we there yet? American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 190(2), 222–230. Portico. https://doi.org/10.1002/ajmg.c.31988
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