P186: Cantu syndrome: Expanding the phenotype of this rare autosomal dominant condition
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2023-01-01
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Series: | Genetics in Medicine Open |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2949774423002157 |
_version_ | 1797342041907134464 |
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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 |
collection | DOAJ |
first_indexed | 2024-03-08T10:27:40Z |
format | Article |
id | doaj.art-82f4e25bdc62474fb0b81485a16f414d |
institution | Directory Open Access Journal |
issn | 2949-7744 |
language | English |
last_indexed | 2024-03-08T10:27:40Z |
publishDate | 2023-01-01 |
publisher | Elsevier |
record_format | Article |
series | Genetics in Medicine Open |
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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