Related Experiment Videos
The search for molecular defects in genetic disease
1Department of Clinical Genetics, Erasmus University, Rotterdam, The Netherlands.
Acta Geneticae Medicae Et Gemellologiae
|January 1, 1996
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
New names for old disciplines.
Journal of inherited metabolic disease·2002
Noninvasive test for fragile X syndrome, using hair root analysis.
American journal of human genetics·1999
Different targets for the fragile X-related proteins revealed by their distinct nuclear localizations.
Human molecular genetics·1999
Prevalence and forms of congenital anomalies in twins born in Pomeranian District during the period from 1.07.1997 to 31.12.1998. Polish Register of Congenital Anomalies.
Acta geneticae medicae et gemellologiae·2000
Analysis of triple test results in 27 cases of twin pregnancies.
Acta geneticae medicae et gemellologiae·2000
Long-term follow-up study of somatic development in prematurely born twins after life-threatening episodes.
Acta geneticae medicae et gemellologiae·2000
Ultrasound in the diagnosis of twin-to-twin transfusion syndrome--a preliminary report.
Acta geneticae medicae et gemellologiae·2000
From the research on electrophoretical mobility of nuclei in twins.
Acta geneticae medicae et gemellologiae·2000
Neurodevelopmental dysfunction and specific learning disabilities in school-aged twins.
Acta geneticae medicae et gemellologiae·2000
Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.
Italian journal of pediatrics·2026
The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.
Journal of biomedical science·2026