Publications by authors named "Maxim Verlee"

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Haploinsufficient variants in SMAD5 are associated with isolated congenital heart disease.
Dimuthu Alankarage, Iryna Leshchynska, Stephanie Portelli, Alena Sipka, Gillian M Blue, Maxim Verlee

HGG Adv· October 2025

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RNA-sequencing unveils FLT4 splice site variants in variable congenital heart disease.
Maxim Verlee, Erika D'haenens, Laurenz De Cock, Laura Muiño Mosquera, Katya De Groote

Eur J Hum Genet· August 2025

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Correction: RNA-sequencing unveils FLT4 splice site variants in variable congenital heart disease.
Maxim Verlee, Erika D'haenens, Laurenz De Cock, Laura Muiño Mosquera, Katya De Groote

Eur J Hum Genet· August 2025

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Loss-of-Function Variants in Cause a Recognizable Connective Tissue Disorder Characterized by Cutis Laxa and Multiple Herniations.
Maxim Verlee, Aude Beyens, Alper Gezdirici, Elif Yilmaz Gulec, Lore Pottie

Genes (Basel)· March 2021

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