Published in
Wiley, Clinical Genetics, 5-6(101), p. 575-576, 2022
DOI: 10.1111/cge.14124
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The diagnosis of the first‐documented intragenic KANSL1 microduplication patient broadens the genetic spectrum of Koolen de Vries syndrome
Journal article published in 2022 by
Loreto Martorell 
,
Delia Yubero,
Esther Cuatrecasas Capdevila,
Guerau Fernández Isern,
Diana Salinas,
Rosanna Mari Vico,
Mónica Rebollo,
Jordi Muchart,
Judith Armstrong,
Juan Darío Ortigoza‐Escobar
,
Delia Yubero,
Esther Cuatrecasas Capdevila,
Guerau Fernández Isern,
Diana Salinas,
Rosanna Mari Vico,
Mónica Rebollo,
Jordi Muchart,
Judith Armstrong,
Juan Darío Ortigoza‐Escobar
This paper is made freely available by the publisher.
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