Titlebook: Genetic Counseling; Walter Fuhrmann,Friedrich Vogel Textbook 19833rd edition Springer-Verlag New York Inc. 1983 Chromosom.Erbkrankheit.Gen

NEG

Malformations Not Subject to a Simple Mode of Inheritance,ality. In most cases, the answer is simply that the occurrence is accidental and a repetition in the family is as unlikely as lightning striking twice in the same place. This answer satisfies the doctor’s responsibility to reassure the frequently deeply disturbed parents—and it may even be the corre

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剛開(kāi)始

Genetic Prognosis for a Consanguineous Marriage,on. As far as we can tell, it was based on social necessity, for the formation of a society and a civilization is inconceivable without an incest taboo. Historical reasons would probably account for the extension of the incest taboo to other degrees of kinship. Various societies made exceptions; som

AGGER

Exposure to Mutagenic Noxes,e children of persons who have been inordinately exposed to such mutagens is being asked more and more often. To give specific advice about the dangers of a particular mutagen is not always possible on the basis of direct observational data in man. However, the results of experimental mutation resea

ERUPT

Teratogenic Effects During Early Pregnancy, in the primary sense. However, the human geneticist is involved in highly differentiated diagnosis both as to the type and the cause of developmental disturbances, and such questions frequently become a part of genetic counseling. The medication laws require the manufacturers to include appropriate

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Psychological and Social Considerations,l. Genetic counseling is an important part of comprehensive medical care. The number of families asking for this service has increased dramatically in the last few years. This is a result of the rapid development of medical genetics on the one hand and a change in the attitude toward having children

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exact specific risk figures. It is true that the daily practice of medicine sees far fewer situations in which these methods can reasonably be applied than some theoreticians like to think. However, the usefulness of these methods has recently increased, especially in cases of X-chromosomal recessive diseases978-0-387-90715-4978-1-4612-5435-5