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Research | 26 November 2014
Deletion of protein tyrosine phosphatase, non-receptor type 4 (PTPN4) in twins with a Rett syndrome-like phenotype
European Journal of Human Genetics 23 , 1171–1175

Rights & permissionsfor article Deletion of protein tyrosine phosphatase, non-receptor type 4 (<i>PTPN4</i>) in twins with a Rett syndrome-like phenotype . Opens in a new window.
Research | 12 September 2012
14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype
- Carolyn J Ellaway
- , Gladys Ho
- , Elisa Bettella
- , Alisa Knapman
- , Felicity Collins
- , Anna Hackett
- , Fiona McKenzie
- , Artur Darmanian
- , Gregory B Peters
- , Kerry Fagan
- & John Christodoulou
European Journal of Human Genetics 21 , 522–527

Rights & permissionsfor article 14q12 microdeletions excluding <i>FOXG1</i> give rise to a congenital variant Rett syndrome-like phenotype . Opens in a new window.
Research | 6 January 2020 | Open
Efficacy and safety of D,L-3-hydroxybutyrate (D,L-3-HB) treatment in multiple acyl-CoA dehydrogenase deficiency
Genetics in Medicine 22 , 908–916

Rights & permissionsfor article Efficacy and safety of D,L-3-hydroxybutyrate (D,L-3-HB) treatment in multiple acyl-CoA dehydrogenase deficiency . Opens in a new window.

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Deletion of protein tyrosine phosphatase, non-receptor type 4 (PTPN4) in twins with a Rett syndrome-like phenotype

14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype

Efficacy and safety of D,L-3-hydroxybutyrate (D,L-3-HB) treatment in multiple acyl-CoA dehydrogenase deficiency

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Deletion of protein tyrosine phosphatase, non-receptor type 4 (PTPN4) in twins with a Rett syndrome-like phenotype

14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype

Efficacy and safety of D,L-3-hydroxybutyrate (D,L-3-HB) treatment in multiple acyl-CoA dehydrogenase deficiency

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