Sinus pericranii and myoclonic epilepsy: novel features of 3q29 microdeletion syndrome

2015 ◽  
Vol 116 (3) ◽  
pp. 363-364
Author(s):  
Debopam Samanta
Keyword(s):  
Myoclonic Epilepsy ◽  
Microdeletion Syndrome ◽  
Sinus Pericranii ◽  
3Q29 Microdeletion

scholarly journals 3q29 Microdeletion Syndrome: Clinical and Molecular Characterization of a New Syndrome

2005 ◽  
Vol 77 (1) ◽  
pp. 154-160 ◽  
Author(s):  
Lionel Willatt ◽  
James Cox ◽  
John Barber ◽  
Elisabet Dachs Cabanas ◽  
Amanda Collins ◽  
...  
Keyword(s):  
Molecular Characterization ◽  
Microdeletion Syndrome ◽  
3Q29 Microdeletion

Autistic and psychiatric findings associated with the 3q29 microdeletion syndrome: Case report and review

2010 ◽  
Vol 152A (10) ◽  
pp. 2459-2467 ◽  
Author(s):  
Fabiola Quintero-Rivera ◽  
Pantea Sharifi-Hannauer ◽  
Julian A. Martinez-Agosto
Keyword(s):  
Case Report ◽  
Microdeletion Syndrome ◽  
3Q29 Microdeletion

Mutation screening of the 3q29 microdeletion syndrome candidate genes DLG1 and PAK2 in schizophrenia

2011 ◽  
Vol 156 (7) ◽  
pp. 844-849 ◽  
Author(s):  
L.S. Carroll ◽  
H.J. Williams ◽  
J. Walters ◽  
G. Kirov ◽  
M.C. O'Donovan ◽  
...  
Keyword(s):  
Candidate Genes ◽  
Mutation Screening ◽  
Microdeletion Syndrome ◽  
3Q29 Microdeletion

scholarly journals Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication

2008 ◽  
Vol 1 (1) ◽  
pp. 8 ◽  
Author(s):  
Blake C Ballif ◽  
Aaron Theisen ◽  
Justine Coppinger ◽  
Gordon C Gowans ◽  
Joseph H Hersh ◽  
...  
Keyword(s):  
Clinical Phenotype ◽  
Microdeletion Syndrome ◽  
3Q29 Microdeletion

scholarly journals Familial inheritance of the 3q29 microdeletion syndrome: case report and review

2019 ◽  
Vol 12 (1) ◽  
Author(s):  
Wahab A. Khan ◽  
Ninette Cohen ◽  
Stuart A. Scott ◽  
Elaine M. Pereira
Keyword(s):  
Case Report ◽  
Microdeletion Syndrome ◽  
Familial Inheritance ◽  
3Q29 Microdeletion
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