P186: Cantu syndrome: Expanding the phenotype of this rare autosomal dominant condition

Bibliographic Details
Main Authors: Punita Gupta, Lorien King, Leah Fried, Enrique Lopez
Format: Article
Language:English
Published: Elsevier 2023-01-01
Series:Genetics in Medicine Open
Online Access:http://www.sciencedirect.com/science/article/pii/S2949774423002157
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author Punita Gupta
Lorien King
Leah Fried
Enrique Lopez
author_facet Punita Gupta
Lorien King
Leah Fried
Enrique Lopez
author_sort Punita Gupta
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spelling doaj.art-82f4e25bdc62474fb0b81485a16f414d2024-01-27T07:05:20ZengElsevierGenetics in Medicine Open2949-77442023-01-0111100215P186: Cantu syndrome: Expanding the phenotype of this rare autosomal dominant conditionPunita Gupta0Lorien King1Leah Fried2Enrique Lopez3St. Joseph's University Medical CenterSt. Joseph's University Medical CenterSt. Joseph's University Medical CenterSt. Joseph's University Medical Centerhttp://www.sciencedirect.com/science/article/pii/S2949774423002157
spellingShingle Punita Gupta
Lorien King
Leah Fried
Enrique Lopez
P186: Cantu syndrome: Expanding the phenotype of this rare autosomal dominant condition
Genetics in Medicine Open
title P186: Cantu syndrome: Expanding the phenotype of this rare autosomal dominant condition
title_full P186: Cantu syndrome: Expanding the phenotype of this rare autosomal dominant condition
title_fullStr P186: Cantu syndrome: Expanding the phenotype of this rare autosomal dominant condition
title_full_unstemmed P186: Cantu syndrome: Expanding the phenotype of this rare autosomal dominant condition
title_short P186: Cantu syndrome: Expanding the phenotype of this rare autosomal dominant condition
title_sort p186 cantu syndrome expanding the phenotype of this rare autosomal dominant condition
url http://www.sciencedirect.com/science/article/pii/S2949774423002157
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AT leahfried p186cantusyndromeexpandingthephenotypeofthisrareautosomaldominantcondition
AT enriquelopez p186cantusyndromeexpandingthephenotypeofthisrareautosomaldominantcondition