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Publications by S Liechti-Gallati
Clonal Analysis of Human Tumors With M27 Beta, a Highly Informative Polymorphic X Chromosomal Probe.
Journal of Clinical Investigation
Medicine
On the Origin of Deletions and Point Mutations in Duchenne Muscular Dystrophy: Most Deletions Arise in Oogenesis and Most Point Mutations Result From Events in Spermatogenesis.
Journal of Medical Genetics
Genetics
Related publications
Detection of Chromosomal 7 Loss in Myelodysplasia Using an Extremely Polymorphic DNA Probe
British Journal of Cancer
Cancer Research
Oncology
Human Globin Gene Analysis for a Patient With Beta-O/Delta Beta-Thalassemia.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Linkage of the Wiskott-Aldrich Syndrome With Polymorphic DNA Sequences From the Human X Chromosome.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Targeted Imaging of Brain Tumors With a Framework Nucleic Acid Probe
Multiple Oncogenic Mutations and Clonal Relationship in Spatially Distinct Benign Human Epidermal Tumors
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Patterns of Chromosomal Aberrations in Solid Tumors
Recent Results in Cancer Research
Medicine
Cancer Research
Oncology
Ataxias With Autosomal, X-Chromosomal or Maternal Inheritance
Canadian Journal of Neurological Sciences
Medicine
Neurology
X-Ray Energy Spectrometry for Electron-Probe Analysis.
The Journal of the Geological Society of Japan
A Child With 45,x/46,X,del(Y)(q12) Identified With a Y-Specific Probe
Fertility and Sterility
Gynecology
Reproductive Medicine
Obstetrics
