This work concentrates on fragile X syndrome and cancer genetics, examining the parallel development and application of both molecular and cytogenetic technologies for the diagnosis and treatment of these genetic disorders.
Reihe
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Verlagsort
Verlagsgruppe
Zielgruppe
Für höhere Schule und Studium
Für Beruf und Forschung
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Maße
Höhe: 235 mm
Breite: 154 mm
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ISBN-13
978-0-471-56098-2 (9780471560982)
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Schweitzer Klassifikation
The Fragile X Syndrome - Clinical Overview; Laboratory Aspects of Prenatal Fra(X) Detection; Molecular Markers of Fragile X: Recent Research Developments; Molecular Markers of Fragile X: Application to Males at Risk in Fragile X Families; Genetic Epidemiology of the Fragile X Syndrome With Special Reference to Genetic Counselling; Cytogenetics of Human Neoplasias.
