3q29 microdeletion
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scholarly journals Prenatal detection of a 3q29 microdeletion in a fetus with ventricular septum defect

Medicine ◽  
2021 ◽  
Vol 100 (1) ◽  
pp. e24224
Author(s):  
Fagui Yue ◽  
Shu Deng ◽  
Qi Xi ◽  
Yuting Jiang ◽  
Jing He ◽  
...  
Keyword(s):  
Ventricular Septum ◽  
Ventricular Septum Defect ◽  
Prenatal Detection ◽  
3Q29 Microdeletion

Paroxysmal oculogyric dystonia associated with a de novo 3q29 microdeletion

2020 ◽  
Vol 30 (4) ◽  
pp. 119-123
Author(s):  
Harsimran Kaur ◽  
Robyn P. Thom ◽  
Ann M. Neumeyer ◽  
Colleen G. Bilancia ◽  
Shirley H. Wray ◽  
...  
Keyword(s):  
De Novo ◽  
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

3q29 microdeletion syndrome: Cognitive and behavioral phenotype in four patients

2013 ◽  
Vol 161 (12) ◽  
pp. 3018-3022 ◽  
Author(s):  
Santina Città ◽  
Serafino Buono ◽  
Donatella Greco ◽  
Concetta Barone ◽  
Enrico Alfei ◽  
...  
Keyword(s):  
Behavioral Phenotype ◽  
Microdeletion Syndrome ◽  
3Q29 Microdeletion

scholarly journals Co-occurrence of autism, childhood psychosis, and intellectual disability associated with a de novo 3q29 microdeletion

2013 ◽  
Vol 161 (4) ◽  
pp. 845-849 ◽  
Author(s):  
Angela Sagar ◽  
Jeffrey R. Bishop ◽  
D. Clare Tessman ◽  
Steve Guter ◽  
Christa L. Martin ◽  
...  
Keyword(s):  
Intellectual Disability ◽  
De Novo ◽  
Childhood Psychosis ◽  
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
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