Exome sequencing identifies de novo pathogenic variants in
FBN1
and
TRPS1
in a patient with a complex connective tissue phenotype
Supplemental Material
Files in this Data Supplement:
Supplemental Figure S1A.pdf
Supplemental Figure S1B.pdf
Supplemental Figure S1C.pdf
Supplemental Figure S1D.pdf
Supplemental Figure S1E.pdf
Supplemental Figure S1F.pdf
Supplemental Figure S2A.jpeg
Supplemental Figure S2B.jpeg
Supplemental Figure S2C.jpeg
Supplemental Figure S2D.jpeg
Supplemental Figure S2E.jpeg
Supplemental Figure S3A.jpg
Supplemental Figure S3B.jpg
Supplemental Figure S3C.jpg
Supplemental Figure S3D.jpg
Supplemental Figure S3E.jpg
Supplemental Figure S3F.jpg
Supplemental Figure S3G.jpg
Supplemental Figure S3H.jpg
Supplemental Legends.docx
Supplemental Table S1.xls
