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Mutation analysis of FOXF2 in patients with disorders of sex development (DSD) in combination with cleft palate
U. Jochumsen,
R. Werner
, N. Miura, A. Richter-Unruh,
O. Hiort
, P. M. Holterhus
Clinic of Pediatric and Adolescent Medicine
Hamamatsu University School of Medicine
Endokrinologikum Ruhr
University of Kiel
7
Citations (Scopus)
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Dive into the research topics of 'Mutation analysis of FOXF2 in patients with disorders of sex development (DSD) in combination with cleft palate'. Together they form a unique fingerprint.
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Biochemistry, Genetics and Molecular Biology
DNA Sequence
100%
Gene Mutation
66%
Exon
66%
Transcription Factor
33%
Messenger RNA
33%
Sex Differentiation
33%
Coding Region
33%
Androgen Synthesis
33%
Untranslated Region
33%
Silent Mutation
33%
Alanine
33%
Knockout Mouse
33%
Medicine and Dentistry
Disorders of Sex Development
100%
Cleft Palate
100%
DNA Sequence
60%
Exon
40%
Gene Mutation
40%
Genomic DNA
20%
Hypoplasia
20%
Palate
20%
Androgen
20%
Transcription Factor
20%
Alanine
20%
Untranslated Region
20%
Silent Mutation
20%
Neuroscience
Palate
100%
Cleft
100%
DNA Sequencing
60%
Androgen
40%
Exon
40%
Gene Mutation
40%
Tubercle
20%
Messenger RNA
20%
Genomic DNA
20%
Hypoplasia
20%