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Three-dimensional facial morphology in Cantú syndrome
Helen I. Roessler
, Kathleen Shields
,
Dorothy K. Grange
, Nine V.A.M. Knoers
, Gijs van Haaften
, Peter Hammond
, Mieke M. van Haelst
Division of Genetics and Genomic Medicine
Center for the Investigation of Membrane Excitability Diseases
Institute of Clinical and Translational Sciences (ICTS)
Research output
:
Contribution to journal
›
Article
›
peer-review
5
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Scopus citations
Overview
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Medicine and Dentistry
Genetic Disorder
100%
Diagnostic Error
100%
Molecular Diagnosis
100%
Face Malformation
100%
Dysmorphology
100%
Adenosine Triphosphate
50%
Chondrodysplasia
50%
Adenosine Triphosphate Sensitive Potassium Channel
50%
Genetic Counseling
50%
Photograph
50%
Hypertrichosis
50%
KCNJ8
50%
Cardiovascular Malformation
50%
Coarse Facial Features
50%
Long Philtrum
50%
Diseases
50%
Morphometric Analysis
50%
Keyphrases
Cant
100%
Three-dimensional (3D)
100%
Facial Morphology
100%
Molecular Diagnostics
25%
Facial Anomalies
25%
ABCC9
25%
Facial Dysmorphology
25%
Pore-forming Subunit
12%
Genetic Disease
12%
Pathogenic Variants
12%
Early Diagnosis
12%
Genetic Syndromes
12%
Gender-specific
12%
Clinical Diagnosis
12%
ATP-sensitive Potassium Channel
12%
Cardiovascular Abnormalities
12%
Genetic Counseling
12%
Morphometric Analysis
12%
Osteochondrodysplasias
12%
3D Image
12%
KCNJ8
12%
Associated Anomalies
12%
Long philtrum
12%
Nasal Bridge
12%
Epicanthal Fold
12%
Coarse Facial Features
12%
Congenital Hypertrichosis
12%
Facial Image
12%
Face Shape
12%
Reduced Stress
12%
Biochemistry, Genetics and Molecular Biology
ABCC9
100%
Genetics
50%
Genetic Disorder
50%
Adenosine Triphosphate
50%
Genetic Counseling
50%
KCNJ8
50%
Adenosine Triphosphate Sensitive Potassium Channel
50%