Article ISI SCOPUS
Orphanet Journal of Rare Diseases  (2013)

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, MJM; Afenjar, A; Albrecht, B; Allanson, JE; Balestri, P; Ben-Omran, T; Brancati, F; et. al.

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Título según WOS: The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP
Título según SCOPUS: The phenotype of Floating-Harbor syndrome: Clinical characterization of 52 individuals with mutations in exon 34 of SRCAP
Título de la Revista: Orphanet Journal of Rare Diseases
Volumen: 8
Número: 1
Editorial: BIOMED CENTRAL LTD
Fecha de publicación: 2013
Idioma: English
URL: http://www.ojrd.com/content/8/1/63
DOI:

10.1186/1750-1172-8-63
Notas: ISI, SCOPUS