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References (6)
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F. Pugnaloni, P. Versacci, B. Marino, M. Digilio (2021)
Atrioventricular canal defect is the classic congenital heart disease in Bardet–Biedl syndromeAnnals of Human Genetics, 85
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Evren Gumus, E. Tuncez, Ozlem Oz, Merve Guvenc (2020)
Clinical and exome sequencing findings in seven children with Bardet–Biedl syndrome from TurkeyAnnals of Human Genetics, 85
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(2021)
University of Washington. Retrieved from: https://www.ncbi.nlm.nih.gov/ books/NBK1363 -
M. Digilio, G. Calcagni, A. Luca, V. Guida, B. Marino (2019)
Atrioventricular canal defect as partial expression of heterotaxia in patients with Bardet-Biedl syndrome.The Journal of pediatrics
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Andrew Olson, Anthony Krentz, K. Finta, Uzoma Okorie, R. Haws (2019)
Thoraco‐Abdominal Abnormalities in Bardet‐Biedl Syndrome: Situs Inversus and HeterotaxyThe Journal of Pediatrics, 204
- Publisher
- Wiley
- Copyright
- © 2021 John Wiley & Sons Ltd/University College London
- ISSN
- 0003-4800
- eISSN
- 1469-1809
- DOI
- 10.1111/ahg.12420
- Publisher site
- See Article on Publisher Site
Abstract
Journal
Annals of Human Genetics – Wiley
Published: May 1, 2021