Details van artikel 264 van 939 gevonden artikelen
P588: De novo and inherited variants in DDX39B cause a novel neurodevelopmental syndrome characterized by hypotonia, epilepsy, and short stature
Titel:
P588: De novo and inherited variants in DDX39B cause a novel neurodevelopmental syndrome characterized by hypotonia, epilepsy, and short stature
Auteur:
Booth, Kevin Jangam, Sharayu Man Chun Chui, Martin Treat, Kayla Graziani, Lorenzo Soldano, Alessia White, Kerry Christensen, Celanie Lynnes, Ty Yamamoto, Shinya Kanca, Oguz Tsang, Mandy Lynch, Sally Mullegama, Sureni Baptista, Julia Iancu, Daniela Joss, Shelag CY Mak, Christopher Kwong, Anna Bellen, Hugo Conboy, Erin Sanges, Remo Wangler, Michael F. Hon-Yin Chung, Brian Vetrini, Francesco
Verschenen in:
Genetics in medicine open
Paginering:
Jaargang 2 () nr. S1 pagina's p.
Jaar:
2024
Inhoud:
Uitgever:
Published by Elsevier B.V.
Bronbestand:
Elektronische Wetenschappelijke Tijdschriften
Details van artikel 264 van 939 gevonden artikelen