Related Experiment Videos
Phenylalanine hydroxylase deficiency in a population in Germany: mutational profile and nine novel mutations
P Guldberg1, R Mallmann, K F Henriksen
1Danish Center for Human Genome Research, John F. Kennedy Institute, Glostrup, Denmark.
Human Mutation
|January 1, 1996
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Forensic postmortem computed tomography in suspected unnatural adult deaths.
European journal of radiology·2020
Effectiveness of aqueous and hydroalcoholic extracts of Acanthospermum australe (Loefl.) Kuntze against diarrhea-inducing bacteria.
Brazilian journal of biology = Revista brasleira de biologia·2018
E- to N-cadherin switch in melanoma is associated with decreased expression of phosphatase and tensin homolog and cancer progression.
The British journal of dermatology·2013
T-cell receptor clonotype mapping using denaturing gradient gel electrophoresis : analysis of clonal T-cell responses in melanoma.
Methods in molecular medicine·2012
Risk for contralateral breast cancer among carriers of the CHEK2*1100delC mutation in the WECARE Study.
British journal of cancer·2008
Complete genome sequences of Trueperella abortisuis isolated from porcine abortion cases in Kumamoto, Japan.
Microbiology resource announcements·2026
Comparative genomics reveals hidden genetic determinants of wheat gluten quality.
Journal of integrative plant biology·2026
Genome-wide meta-analysis dissects the genetic basis and health implications of circulating taurine.
Functional & integrative genomics·2026
Investigating the effects of missense mutations on the dual Ras/Rap activation mechanism of SYNGAP1 using molecular modelling.
Journal of structural biology: X·2026