Mutation as a Cause of Genetic Disease [and Discussion]

Mutational changes can be conveniently classified into two sorts: those that appear to involve single genes and are generally referred to as gene mutations, and those that involve chromosomal segments containing many genes, or even whole chromosomes, and are referred to as chromosomal mutations. Bot...

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Veröffentlicht in:	Philosophical transactions of the Royal Society of London. Series B, Biological sciences Biological sciences, 1988-06, Vol.319 (1194), p.325-340
Hauptverfasser:	Evans, H. J., Worton, R.
Format:	Artikel
Sprache:	eng
Schlagworte:	Abortion, Spontaneous - genetics Adult Aneuploidy Biological and medical sciences Blood Chromosome Aberrations Chromosome Disorders Chromosomes Down Syndrome - etiology Down Syndrome - genetics Female Fetal Death - genetics General aspects. Genetic counseling Genes Genetic diseases Genetic Diseases, Inborn - genetics Genetic mutation Humans Infant, Newborn Leukocytes Lymphocytes Maternal Age Medical genetics Medical sciences Mutagens Mutation Pregnancy Somatic cells
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