Identification of a deletion containing TBX4 in a neonate with acinar dysplasia by rapid exome sequencing-Reference-Cited by-同舟云学术

Identification of a deletion containing TBX4 in a neonate with acinar dysplasia by rapid exome sequencing

Author:

German Kendell¹^ORCID,Deutsch Gail H.²,Freed Amanda S.³,Dipple Katrina M.⁴⁵,Chabra Shilpi¹,Bennett James T.⁴⁶

Affiliation:

1. Department of Pediatrics; University of Washington; Seattle Washington

2. Department of Pathology; Seattle Children's Hospital and University of Washington; Seattle Washington

3. Department of Medicine, Division of Medical Genetics; University of Washington; Seattle Washington

4. Department of Pediatrics, Division of Genetic Medicine; University of Washington; Seattle Washington

5. Center for Clinical and Translational Research; Seattle Children's Research Institute; Seattle Washington

6. Center for Developmental Biology and Regenerative Medicine; Seattle Children's Research Institute; Seattle Washington

Funder

Arnold Lee Smith Endowed Professorship for Research Faculty

Burroughs Wellcome Fund Career Award for Medical Scientists

National Institute of General Medical Sciences of the National Institutes of Health

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

Reference21 articles.

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5. Molecular Function and Contribution of TBX4 in Development and Disease;American Journal of Respiratory and Critical Care Medicine;2023-04-01