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Van der woude syndrome
T. Elien
, D. N. Kamilla
,
E. I. Auerkari
Department of Oral Biology
Research output
:
Contribution to journal
›
Conference article
›
peer-review
1
Citation (Scopus)
Overview
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Keyphrases
Van Der Woude Syndrome
100%
Orofacial Clefts
88%
IRF6
55%
GRHL3
33%
Syndromic
22%
Periderm
22%
Live Birth
11%
Learning Development
11%
Review Authors
11%
Cleft Palate
11%
Cognitive Difficulties
11%
Autosomal Dominant
11%
Dominant Pattern
11%
Craniofacial Birth Defects
11%
Learning Disabilities
11%
Structural Chromosomal Aberrations
11%
Cleft Palate Alone
11%
IRF6 Gene
11%
Coding mutation
11%
Author's Will
11%
Non-syndromic
11%
Delayed Language Development
11%
Lower Lip pits
11%
Mild Cognitive
11%
Medicine and Dentistry
Van Der Woude Syndrome
100%
Cleft
88%
Interferon Regulatory Factor 6
66%
Physical Disease by Body Function
11%
Prevalence
11%
Maturation
11%
Cleft Palate
11%
Learning Disorder
11%
Congenital Malformation
11%
Cleft Lip with or without Cleft Palate
11%
Chromosome Aberration
11%
Language Delay
11%
Autosomal Dominant Inheritance
11%
Pharmacology, Toxicology and Pharmaceutical Science
Van Der Woude Syndrome
100%
Interferon Regulatory Factor 6
66%
Physical Disease by Body Function
11%
Prevalence
11%
Syndrome
11%
Congenital Malformation
11%
Cleft Palate
11%
Chromosome Aberration
11%
Cleft Lip with or without Cleft Palate
11%
Learning Disorder
11%
Language Delay
11%
Biochemistry, Genetics and Molecular Biology
IRF6
100%
Maturation
16%
Prevalence
16%
Autosomal Dominant Inheritance
16%
Language Development
16%
Chromosomal Disorder
16%