Further Clinical and Molecular Delineation of the 15Q24 Microdeletion Syndrome

AuthID
P-002-DMZ
30
Author(s)
Rosenfeld, JA
·
Cox, VA
·
Firth, HV
·
Willatt, L
·
Wheeler, P
·
[+3]·
[+1]·
[+1]·
[+5]·
Smith, W
·
Smith, R
·
Paull, L
·
Rosenbaum, KN
·
Lamb, A
·
Eichler, EE
Document Type
Article
Year published
2012
Published
in JOURNAL OF MEDICAL GENETICS, ISSN: 0022-2593
Volume: 49, Issue: 2, Pages: 110-118 (9)
Indexing
Publication Identifiers
Pubmed: 22180641
SCOPUS: 2-s2.0-84862908076
Wos: WOS:000299308900008
Source Identifiers
ISSN: 0022-2593
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Name Order Name   Name Order Name   Name Order Name
1 Mefford, HC;   2 Rosenfeld, JA;   3 Shur, N;
4 Slavotinek, AM;   5 Cox, VA;   6 Hennekam, RC;
7 Firth, HV;   8 Willatt, L;   9 Wheeler, P;
10 Morrow, EM;   11 Cook, J;   12 Sullivan, R;
13 Oh, A;   14 McDonald, MT;   15 Zonana, J;
16 Keller, K;   17 Hannibal, MC;   18 Ball, S;
19 Kussmann, J;   20 Gorski, J;   21 Zelewski, S;
22 Banks, V;   23 Smith, W;   24 Smith, R;
25 Paull, L;   26 Rosenbaum, KN;   27 Amor, DJ;
28 Silva, J;   29 Lamb, A;   30 Eichler, EE;