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Fetal MR imaging of atelosteogenesis type II (AO-II).
Miller E, Blaser S, Miller S, Keating S, Thompson M, Unger S, Toi A, Berger H, Chong K. Miller E, et al. Among authors: chong k. Pediatr Radiol. 2008 Dec;38(12):1345-9. doi: 10.1007/s00247-008-0974-y. Epub 2008 Aug 21. Pediatr Radiol. 2008. PMID: 18716767
Diagnostic utility of microarray testing in pregnancy loss.
Rosenfeld JA, Tucker ME, Escobar LF, Neill NJ, Torchia BS, McDaniel LD, Schultz RA, Chong K, Chitayat D. Rosenfeld JA, et al. Among authors: chong k. Ultrasound Obstet Gynecol. 2015 Oct;46(4):478-86. doi: 10.1002/uog.14866. Epub 2015 Sep 1. Ultrasound Obstet Gynecol. 2015. PMID: 25846569 Free article.
Warsaw breakage syndrome: Further clinical and genetic delineation.
Alkhunaizi E, Shaheen R, Bharti SK, Joseph-George AM, Chong K, Abdel-Salam GMH, Alowain M, Blaser SI, Papsin BC, Butt M, Hashem M, Martin N, Godoy R, Brosh RM Jr, Alkuraya FS, Chitayat D. Alkhunaizi E, et al. Among authors: chong k. Am J Med Genet A. 2018 Nov;176(11):2404-2418. doi: 10.1002/ajmg.a.40482. Epub 2018 Sep 14. Am J Med Genet A. 2018. PMID: 30216658 Free PMC article.
Gain-of-function variants in the ODC1 gene cause a syndromic neurodevelopmental disorder associated with macrocephaly, alopecia, dysmorphic features, and neuroimaging abnormalities.
Rodan LH, Anyane-Yeboa K, Chong K, Klein Wassink-Ruiter JS, Wilson A, Smith L, Kothare SV, Rajabi F, Blaser S, Ni M, DeBerardinis RJ, Poduri A, Berry GT. Rodan LH, et al. Among authors: chong k. Am J Med Genet A. 2018 Dec;176(12):2554-2560. doi: 10.1002/ajmg.a.60677. Epub 2018 Nov 26. Am J Med Genet A. 2018. PMID: 30475435
Brain and Placental Pathology in Fetal COL4A1 Related Disease.
Shannon P, Hum C, Parks T, Schauer GM, Chitayat D, Chong K, Shinar S, Blaser S, Moore G, Van Mieghem T. Shannon P, et al. Among authors: chong k. Pediatr Dev Pathol. 2021 May-Jun;24(3):175-186. doi: 10.1177/1093526620984083. Epub 2021 Jan 21. Pediatr Dev Pathol. 2021. PMID: 33475042
1,558 results