Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1988 Oct;113(4):703-6.
doi: 10.1016/s0022-3476(88)80384-6.

A unique association of short stature, dysmorphic features, and speech impairment (Floating-Harbor syndrome)

P L Robinson  1 , M Shohat, R M Winter, W J Conte, D Gordon-Nesbitt, M Feingold, Z Laron, D L Rimoin
Affiliations

A unique association of short stature, dysmorphic features, and speech impairment (Floating-Harbor syndrome)

P L Robinson et al. J Pediatr. 1988 Oct.
No abstract available

PubMed Disclaimer

Similar articles

See all similar articles

Cited by

  • Rubinstein-Taybi Syndrome: A Rare Case Report.
    Tomar SS, Supekar BB, Mukhi J, Singh RP. Tomar SS, et al. Indian Dermatol Online J. 2020 Mar 9;11(2):258-260. doi: 10.4103/idoj.IDOJ_108_19. eCollection 2020 Mar-Apr. Indian Dermatol Online J. 2020. PMID: 32477995 Free PMC article. No abstract available.
  • Floating-Harbor Syndrome: Presentation of the First Romanian Patient with a SRCAP Mutation and Review of the Literature.
    Budisteanu M, Bögershausen N, Papuc SM, Moosa S, Thoenes M, Riga D, Arghir A, Wollnik B. Budisteanu M, et al. Balkan J Med Genet. 2018 Oct 29;21(1):83-86. doi: 10.2478/bjmg-2018-0005. eCollection 2018 Jun. Balkan J Med Genet. 2018. PMID: 30425916 Free PMC article.
  • The emerging role of chromatin remodelers in neurodevelopmental disorders: a developmental perspective.
    Mossink B, Negwer M, Schubert D, Nadif Kasri N. Mossink B, et al. Cell Mol Life Sci. 2021 Mar;78(6):2517-2563. doi: 10.1007/s00018-020-03714-5. Epub 2020 Dec 2. Cell Mol Life Sci. 2021. PMID: 33263776 Free PMC article. Review.
  • The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP.
    Nikkel SM, Dauber A, de Munnik S, Connolly M, Hood RL, Caluseriu O, Hurst J, Kini U, Nowaczyk MJ, Afenjar A, Albrecht B, Allanson JE, Balestri P, Ben-Omran T, Brancati F, Cordeiro I, da Cunha BS, Delaney LA, Destrée A, Fitzpatrick D, Forzano F, Ghali N, Gillies G, Harwood K, Hendriks YM, Héron D, Hoischen A, Honey EM, Hoefsloot LH, Ibrahim J, Jacob CM, Kant SG, Kim CA, Kirk EP, Knoers NV, Lacombe D, Lee C, Lo IF, Lucas LS, Mari F, Mericq V, Moilanen JS, Møller ST, Moortgat S, Pilz DT, Pope K, Price S, Renieri A, Sá J, Schoots J, Silveira EL, Simon ME, Slavotinek A, Temple IK, van der Burgt I, de Vries BB, Weisfeld-Adams JD, Whiteford ML, Wierczorek D, Wit JM, Yee CF, Beaulieu CL; FORGE Canada Consortium; White SM, Bulman DE, Bongers E, Brunner H, Feingold M, Boycott KM. Nikkel SM, et al. Orphanet J Rare Dis. 2013 Apr 27;8:63. doi: 10.1186/1750-1172-8-63. Orphanet J Rare Dis. 2013. PMID: 23621943 Free PMC article.
  • The defining DNA methylation signature of Floating-Harbor Syndrome.
    Hood RL, Schenkel LC, Nikkel SM, Ainsworth PJ, Pare G, Boycott KM, Bulman DE, Sadikovic B. Hood RL, et al. Sci Rep. 2016 Dec 9;6:38803. doi: 10.1038/srep38803. Sci Rep. 2016. PMID: 27934915 Free PMC article.
See all "Cited by" articles

Publication types

LinkOut - more resources