Cited by

• [Floating-Harbor syndrome: a case report and literature review].

  Li RM, Lu YC, Li Z, Wang JY, Chang J, Lei SQ, Zeng Q, Sang YM. Li RM, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2019 Dec;21(12):1208-1211. doi: 10.7499/j.issn.1008-8830.2019.12.011. Zhongguo Dang Dai Er Ke Za Zhi. 2019. PMID: 31874661 Free PMC article. Review. Chinese.
• A neurodevelopmental disorder caused by a novel de novo SVA insertion in exon 13 of the SRCAP gene.

  Zhao B, Madden JA, Lin J, Berry GT, Wojcik MH, Zhao X, Brand H, Talkowski M, Lee EA, Agrawal PB. Zhao B, et al. Eur J Hum Genet. 2022 Sep;30(9):1083-1087. doi: 10.1038/s41431-022-01137-3. Epub 2022 Jun 30. Eur J Hum Genet. 2022. PMID: 35768521 Free PMC article.
• Novel genotypes and phenotypes among Chinese patients with Floating-Harbor syndrome.

  Zhang S, Chen S, Qin H, Yuan H, Pi Y, Yang Y, Huang H, Li G, Sun Y, Wang Z, Ma H, Fu X, Zhou T, Wang J, Zhang H, Shen Y. Zhang S, et al. Orphanet J Rare Dis. 2019 Jun 14;14(1):144. doi: 10.1186/s13023-019-1111-8. Orphanet J Rare Dis. 2019. PMID: 31200758 Free PMC article.
• The first Korean case with Floating-Harbor syndrome with a novel SRCAP mutation diagnosed by targeted exome sequencing.

  Choi EM, Lee DH, Kang SJ, Shim YJ, Kim HS, Kim JS, Jeong JI, Ha JS, Jang JH. Choi EM, et al. Korean J Pediatr. 2018 Dec;61(12):403-406. doi: 10.3345/kjp.2018.06289. Epub 2018 Sep 16. Korean J Pediatr. 2018. PMID: 30304910 Free PMC article.
• Molecular Genetics and Pathogenesis of the Floating Harbor Syndrome: Case Report of Long-Term Growth Hormone Treatment and a Literature Review.

  Turkunova ME, Barbitoff YA, Serebryakova EA, Polev DE, Berseneva OS, Bashnina EB, Baranov VS, Glotov OS, Glotov AS. Turkunova ME, et al. Front Genet. 2022 May 18;13:846101. doi: 10.3389/fgene.2022.846101. eCollection 2022. Front Genet. 2022. PMID: 35664296 Free PMC article.