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Cornelia de Lange syndrome
M I Boyle, C Jespersgaard, K Brøndum-Nielsen, A-M Bisgaard,
Z Tümer
Department of Clinical Medicine
Medical Genetics Program
77
Citations (Scopus)
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Dive into the research topics of 'Cornelia de Lange syndrome'. Together they form a unique fingerprint.
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Medicine and Dentistry
Congenital Malformation
100%
De Lange Syndrome
100%
Growth Retardation
50%
Structural Protein
50%
Chromosome 3
50%
Diseases
50%
Genetic Counseling
50%
Urogenital Tract Malformation
50%
Histone Deacetylase 8
50%
Genetic Disorder
50%
Postnatal Growth
50%
Upper Limb
50%
Prenatal Growth
50%
Clinical Feature
50%
Diaphragm Hernia
50%
Hirsutism
50%
Gastroesophageal Reflux
50%
Facies
50%
Biochemistry, Genetics and Molecular Biology
Genetic Counseling
100%
Schizosaccharomyces pombe
100%
Intellectual Disability
100%
Chromosome 3
100%
Prenatal Growth
100%
Histone Deacetylase
100%
Structural Protein
100%
RAD21
100%
Genetics
100%
Postnatal Growth
100%
Keyphrases
Structural Maintenance of Chromosomes
50%
Radiation Sensitivity
25%
Hirsutism
25%
Congenital Anomalies
25%
Schizosaccharomyces Pombe
25%
Chromosome 3
25%
Postnatal Diagnosis
25%
Prenatal Diagnosis
25%
RAD21
25%
Defect Diagnosis
25%
Genetic Defects
25%
Gastroesophageal Reflux Disease
25%
HDAC8
25%
Intellectual Disability
25%
Genetic Counseling
25%
Intrauterine Growth Retardation
25%
Distinctive Facial Features
25%
Human Homolog
25%
Multiple Organs
25%
Mild Phenotype
25%
Pyloric Stenosis
25%
Prenatal Growth
25%
Clinical Features
25%
Malformation
25%
Diaphragmatic Hernia
25%
Heart Defects
25%
Upper Limb
25%