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Olaf Mook
Olaf Mook
Desbuquois Dysplasia
Endocrinology
Internal medicine
XYLT1
Phenotype
1
Papers
9
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Complete and partial XYLT1 deletion in a patient with neonatal short limb skeletal dysplasia.
2016
American Journal of Medical Genetics Part A
Silvana van Koningsbruggen
Hennie Knoester
Roel Bakx
Olaf Mook
Lia Knegt
Jan-Maarten Cobben
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Citations (9)
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