Identification of a new familial case of 3q29 deletion syndrome associated with cleft lip and palate via whole‐exome sequencing-Reference-Cited by-同舟云学术

Identification of a new familial case of 3q29 deletion syndrome associated with cleft lip and palate via whole‐exome sequencing

Published:2022-11 Issue:1 Volume:191 Page:205-219
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:American J of Med Genetics Pt A

Author:

Biedziak Barbara¹^ORCID,Dąbrowska Justyna²^ORCID,Szponar‐Żurowska Anna¹^ORCID,Bukowska‐Olech Ewelina³^ORCID,Jamsheer Aleksander³^ORCID,Mojs Ewa⁴^ORCID,Mulle Jennifer⁵^ORCID,Płoski Rafał⁶^ORCID,Mostowska Adrianna²^ORCID

Affiliation:

1. Department of Orthodontics and Craniofacial Anomalies Poznan University of Medical Sciences Poznan Poland

2. Department of Biochemistry and Molecular Biology Poznan University of Medical Sciences Poznan Poland

3. Department of Medical Genetics Poznan University of Medical Sciences Poznan Poland

4. Department of Clinical Psychology Poznan University of Medical Sciences Poznan Poland

5. Psychiatry Robert Wood Johnson Medical School, Rutgers University New Brunswick New Jersey USA

6. Department of Medical Genetics Warsaw Medical University Warsaw Poland

Funder

European Social Fund

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.63015

Reference43 articles.

1. Genome-Wide Association Study (GWAS) of dental caries in diverse populations

2. Psychiatric-disorder-related behavioral phenotypes and cortical hyperactivity in a mouse model of 3q29 deletion syndrome

3. 22q11.21 Deletion Syndromes: A Review of Proximal, Central, and Distal Deletions and Their Associated Features

4. Craniofacial Dysmorphogenesis Including Cleft Palate in Mice with an Insertional Mutation in the discs large Gene

5. A large multiethnic GWAS meta-analysis of cataract identifies new risk loci and sex-specific effects

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