A Novel Microdeletion Syndrome at 3Q13.31 Characterised by Developmental Delay, Postnatal Overgrowth, Hypoplastic Male Genitals, and Characteristic Facial Features

AuthID
P-002-DMY
35
Author(s)
Molin, AM
·
Andrieux, J
·
Koolen, DA
·
Malan, V
·
Carella, M
·
Colleaux, L
·
Cormier Daire, V
·
David, A
·
[+5]·
[+6]·
[+2]·
[+1]·
[+1]·
Darling, LR
·
Rosenberg, C
·
Sa, J
·
Vallee, L
·
Vincent Delorme, C
·
Zelante, L
·
Bondeson, ML
·
Anneren, G
Document Type
Article
Year published
2012
Published
in JOURNAL OF MEDICAL GENETICS, ISSN: 0022-2593
Volume: 49, Issue: 2, Pages: 104-109 (6)
Indexing
Publication Identifiers
Pubmed: 22180640
Scopus: 2-s2.0-84856007083
Wos: WOS:000299308900007
Source Identifiers
ISSN: 0022-2593
Export Publication Metadata
Marked List
Info
At this moment we don't have any links to full text documens.
Name Order Name   Name Order Name   Name Order Name
1 Molin, AM;   2 Andrieux, J;   3 Koolen, DA;
4 Malan, V;   5 Carella, M;   6 Colleaux, L;
7 Cormier Daire, V;   8 David, A;   9 de Leeuw, N;
10 Delobel, B;   11 Duban Bedu, B;   12 Fischetto, R;
13 Flinter, F;   14 Kjaergaard, S;   15 Kok, F;
16 Krepischi, AC;   17 Le Caignec, C;   18 Ogilvie, CM;
19 Maia, S;   20 Mathieu Dramard, M;   21 Munnich, A;
22 Palumbo, O;   23 Papadia, F;   24 Pfundt, R;
25 Reardon, W;   26 Receveur, A;   27 Rio, M;
28 Darling, LR;   29 Rosenberg, C;   30 Sa, J;
31 Vallee, L;   32 Vincent Delorme, C;   33 Zelante, L;
34 Bondeson, ML;   35 Anneren, G;