The Phenotype of Floating-Harbor Syndrome: Clinical Characterization of 52 Individuals with Mutations in Exon 34 of Srcap

AuthID
 P-005-1G5
68
Author(s)
Dauber, A
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1
Group Author(s)
FORGE Canada Consortium
Document Type
Article
Year published
2013
Published
in ORPHANET JOURNAL OF RARE DISEASES, ISSN: 1750-1172
Volume: 8, Issue: 1, Pages: 63 (9)
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Publication Identifiers
Pubmed: 23621943
SCOPUS: 2-s2.0-84876691492
Wos: WOS:000319314600001
Source Identifiers
ISSN: 1750-1172
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All authors
Name Order Name   Name Order Name   Name Order Name
1 Nikkel, SM;   2 Dauber, A;   3 de Munnik, S;
4 Connolly, M;   5 Hood, RL;   6 Caluseriu, O;
7 Hurst, J;   8 Kini, U;   9 Nowaczyk, MJM;
10 Afenjar, A;   11 Albrecht, B;   12 Allanson, JE;
13 Balestri, P;   14 Ben Omran, T;   15 Brancati, F;
16 Cordeiro, I;   17 da Cunha, BS;   18 Delaney, LA;
19 Destree, A;   20 Fitzpatrick, D;   21 Forzano, F;
22 Ghali, N;   23 Gillies, G;   24 Harwood, K;
25 Hendriks, YMC;   26 Heron, D;   27 Hoischen, A;
28 Honey, EM;   29 Hoefsloot, LH;   30 Ibrahim, J;
31 Jacob, CM;   32 Kant, SG;   33 Kim, CA;
34 Kirk, EP;   35 Knoers, NVAM;   36 Lacombe, D;
37 Lee, C;   38 Lo, IFM;   39 Lucas, LS;
40 Mari, F;   41 Mericq, V;   42 Moilanen, JS;
43 Moller, ST;   44 Moortgat, S;   45 Pilz, DT;
46 Pope, K;   47 Price, S;   48 Renieri, A;
49 Sa, J;   50 Schoots, J;   51 Silveira, EL;
52 Simon, MEH;   53 Slavotinek, A;   54 Temple, IK;
55 van der Burgt, I;   56 de Vries, BBA;   57 Weisfeld Adams, JD;
58 Whiteford, ML;   59 Wierczorek, D;   60 Wit, JM;
61 Yee, CFO;   62 Beaulieu, CL;   63 White, SM;
64 Bulman, DE;   65 Bongers, E;   66 Brunner, H;
67 Feingold, M;   68 Boycott, KM;  

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