-
disruption of the SHANK3 gene (also
called ProSAP2). The
following year,
Anderlid et al. (2002),
refined the area in 22q13
presumably responsible for the...
-
Regan R, Kooy RF,
Reyniers E,
Romano C,
Fichera M,
Schinzel A,
Baumer A,
Anderlid BM,
Schoumans J,
Knoers NV, van
Kessel AG,
Sistermans EA,
Veltman JA, Brunner...
- PMID 12504591. S2CID 572407.
Bonaglia MC,
Giorda R, Mani E,
Aceti G,
Anderlid BM,
Baroncini A,
Pramparo T,
Zuffardi O (October 2006). "Identification...
-
Holmberg E, Strömland K,
Soller M,
Mirzaei L,
Djureinovic T,
Robinson K,
Anderlid B,
Schoumans J (Jul 2008). "CHD7
mutation spectrum in 28
Swedish patients...
-
Haeringen A, Aten E,
Friend K,
Liebelt J,
Barnett C, Haan E, Shaw M, Gecz J,
Anderlid BM,
Nordgren A,
Lindstrand A,
Schwartz C, Kooy RF,
Vandeweyer G, Helsmoortel...
- e18. doi:10.1093/brain/awaa431. PMC 7940500. PMID 33351070.
Breckpot J,
Anderlid BM,
Alanay Y,
Blyth M,
Brahimi A, Duban-Bedu B, et al. (January 2016)....
