Novel features of 3q29 deletion syndrome: Results from the 3q29 registry-Reference-Cited by-同舟云学术

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Novel features of 3q29 deletion syndrome: Results from the 3q29 registry

Published:2016-01-06 Issue:4 Volume:170 Page:999-1006
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Glassford Megan R.¹,Rosenfeld Jill A.²,Freedman Alexa A.³,Zwick Michael E.¹⁴,Mulle Jennifer G.¹³,

Affiliation:

1. Department of Human Genetics; Emory University School of Medicine; Atlanta Georgia

2. Department of Molecular and Human Genetics; Baylor College of Medicine; Houston Texas

3. Department of Epidemiology; Rollins School of Public Health, Emory University; Atlanta Georgia

4. Department of Pediatrics; Emory University School of Medicine; Atlanta Georgia

Funder

National Institutes of Health

Emory University Treasure Your Exceptions Fund

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.37537/fullpdf

Reference23 articles.

1. A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk;Antonacci;Nat Genet,2010

2. Characterization of six human disease-associated inversion polymorphisms;Antonacci;Hum Mol Genet,2009

3. Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication;Ballif;Mol Cytogenet,2008

4. 3q29 microdeletion syndrome: Cognitive and behavioral phenotype in four patients;Citta;Am J Med Genet A,2013

5. Familial 3q29 microdeletion syndrome providing further evidence of involvement of the 3q29 region in bipolar disorder;Clayton-Smith;Clin Dysmorphol,2010

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1. Intrapericardial Teratoma and Associated 3q29 Deletion in a Fetus: Case Report;Zeitschrift für Geburtshilfe und Neonatologie;2024-08-20

2. Structural deviations of the posterior fossa and the cerebellum and their cognitive links in a neurodevelopmental deletion syndrome;Molecular Psychiatry;2024-05-14

3. Psychosis spectrum symptoms among individuals with schizophrenia-associated copy number variants and evidence of cerebellar correlates of symptom severity;Psychiatry Research;2024-05

4. Patient-Reported Outcomes in Autosomal Dominant Osteopetrosis: Findings From the Osteopetrosis Registry Study;The Journal of Clinical Endocrinology & Metabolism;2024-04-25

5. Behavioral Phenotypes and Comorbidity in 3q29 Deletion Syndrome: Results from the 3q29 Registry;Journal of Autism and Developmental Disorders;2024-01-12

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