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Acromicric dysplasia
Marfan Syndrome Precision Panel Overview Indications Clinical Utility
Marfan Syndrome
PATIENT INFORMATION (Please Print Or Place ID Label) Last Name First Name MI
Skeletal Manifestations of Marfan Syndrome Associated to Heterozygous R2726W FBN1 Variant: Sibling Case Report and Literature Review Octavio D
Molecular Genetics of the Fibrillinopathies Mélodie Aubart, Louise Benarroch, Pauline Arnaud, Gwenaelle Collod-Beroud, Guillaume Jondeau, Catherine Boileau
A Review of the Type-1 Fibrillinopathies: Pathophysiology
FBN1 Gene Fibrillin 1
Medical & Clinical Case Reports
WES Gene Package Aneurysm.Xlsx
Characterization of Two Novel Intronic Variants Affecting Splicing in FBN1
Marfan Syndrome Diagnostics, Epidemiology, and Aortic Events
Recessive Gene List V2.0
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