Number of items: 2.
2020
Brock, Stefanie ,
Vanderhasselt, Tim ,
Vermaning, Sietske,
Keymolen, Kathelijn ,
Régal, Luc ,
Romaniello, Romina ,
Wieczorek, Dagmar ,
Storm, Tim Matthias,
Schaeferhoff, Karin,
Hehr, Ute,
Kuechler, Alma,
Krägeloh-Mann, Ingeborg,
Haack, Tobias B.,
Kasteleijn, Esmee,
Schot, Rachel,
Mancini, Grazia Maria Simonetta,
Webster, Richard,
Mohammad, Shekeeb ,
Leventer, Richard J.,
Mirzaa, Ghayda,
Dobyns, William B. ,
Bahi-Buisson, Nadia,
Meuwissen, Marije,
Jansen, Anna C. and
Stouffs, Katrien
(2020)
Defining the phenotypical spectrum associated with variants in TUBB2A.
Journal of Medical Genetics 58 (1), pp. 33-40.
Fulltext not available.
Oegema, Renske ,
Barakat, Tahsin Stefan ,
Wilke, Martina,
Stouffs, Katrien ,
Amrom, Dina,
Aronica, Eleonora,
Bahi-Buisson, Nadia,
Conti, Valerio ,
Fry, Andrew E. ,
Geis, Tobias,
Andres, David Gomez,
Parrini, Elena,
Pogledic, Ivana ,
Said, Edith,
Soler, Doriette,
Valor, Luis M.,
Zaki, Maha S. ,
Mirzaa, Ghayda,
Dobyns, William B.,
Reiner, Orly,
Guerrini, Renzo ,
Pilz, Daniela T.,
Hehr, Ute,
Leventer, Richard J.,
Jansen, Anna C. ,
Mancini, Grazia M. S. and
Di Donato, Nataliya
(2020)
International consensus recommendations on the diagnostic work-up for malformations of cortical development.
Nature Reviews Neurology 16 (11), pp. 618-635.
Fulltext not available.
This list was generated on Fri Dec 6 05:13:58 2024 CET.