Whole exome sequencing combined with dynamic ultrasound assessments for fetal skeletal dysplasias: 4 case reports
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference14 articles.
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3. Apert syndrome results from localized mutations of FGFR2 and is allelic with crouzon syndrome.;Wilkie;Nat Genet,1995
4. Apert syndrome - clinical case.;Siminel;Rom J Morphol Embryol,2017
5. Exclusive paternal origin of new mutations in apert syndrome.;Moloney;Nat Genet,1996
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