Associated Papers
The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140 214 UK Biobank participants.
Stefanucci L et al.
Blood, 2023
37647632 (PubMed )
Supplement: BLOOD_BLD-2023-020118-mmc3.xlsx › ST3.3
Identification of A Novel Variant of Filamin A Destroying the Attraction Between Benzene Rings and Sulfhydryl in Developmental Dysplasia of the Hip.
Lu YL et al.
Dna and Cell Biology, 2023
Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms.
Clarke CM et al.
American Journal of Medical Genetics. Part A, 2018
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