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Dialogues in Clinical Neuroscience, ISSN 1294-8322, 2009, Volume 11, Issue 1, pp. 35 - 43
Journal Article
2005, 2nd ed., ISBN 0801880475, xiii, 404
Book
Human Molecular Genetics, ISSN 0964-6906, 10/2015, Volume 24, Issue 1, pp. R24 - R31
Journal Article
Biological Psychiatry, ISSN 0006-3223, 2015, Volume 77, Issue 9, pp. 766 - 768
Journal Article
Nature Genetics, ISSN 1061-4036, 02/2016, Volume 48, Issue 2, pp. 214 - 220
Journal Article
Molecular Autism, ISSN 2040-2392, 2013, Volume 4, Issue 1, pp. 17 - 17
Journal Article
Molecular Autism, ISSN 2040-2392, 2013, Volume 4, Issue 1, pp. 9 - 9
Background: Haploinsufficiency of SHANK3, due to either hemizygous gene deletion (termed 22q13 deletion syndrome or Phelan-McDermid syndrome) or to gene... 
Pharmacotherapy | Individualized medicine | Phelan-McDermid syndrome | Personalized medicine | 22q13 deletion syndrome | GENETICS & HEREDITY | NEUROSCIENCES | Autism | Genetic aspects | Models | Properties | Insulin-like growth factor 1 | Developmental delay
Journal Article