Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Darcie Babcock
Mutation Analysis of Fibrillin-2 (FBN2) and Microfibril Associated Protein-3 (MFAP-3): Two Genes Associated With Congenital Contractural Arachnodactyly (CCA), Also Known as Beal's Syndrome
Related publications
A Novel Splicing Mutation in the FBN2 Gene in a Family With Congenital Contractural Arachnodactyly
Frontiers in Genetics
Genetics
Molecular Medicine
A Novel FBN2 Mutation Cosegregates With Congenital Contractural Arachnodactyly in a Five-Generation Chinese Family
Clinical Case Reports
Medicine
Identification of a Novel Missense FBN2 Mutation in a Chinese Family With Congenital Contractural Arachnodactyly Using Exome Sequencing
PLoS ONE
Multidisciplinary
Contractural Arachnodactyly Versus Marfan's Syndrome.
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Figure 3: Bioinformatics Analysis of Genes Associated With Osteoporosis.
Microfibril Structure Masks Fibrillin-2 in Postnatal Tissues
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Microfibril-Associated Glycoprotein-2 (MAGP-2) Is Specifically Associated With Fibrillin-Containing Microfibrils but Exhibits More Restricted Patterns of Tissue Localization and Developmental Expression Than Its Structural Relative MAGP-1
Journal of Histochemistry and Cytochemistry
Anatomy
Histology
The Arg451Cys-Neuroligin-3 Mutation Associated With Autism Reveals a Defect in Protein Processing
Journal of Neuroscience
Neuroscience
Atrial Standstill in a Pediatric Patient With Associated Caveolin-3 Mutation
HeartRhythm Case Reports
Cardiovascular Medicine
Cardiology
