標(biāo)題: Titlebook: Genetic Counseling; Walter Fuhrmann,Friedrich Vogel Textbook 19762nd edition Springer-Verlag New York Inc. 1976 Mutation.chromosome.counse [打印本頁] 作者: informed 時(shí)間: 2025-3-21 17:28
書目名稱Genetic Counseling影響因子(影響力)
書目名稱Genetic Counseling影響因子(影響力)學(xué)科排名
書目名稱Genetic Counseling網(wǎng)絡(luò)公開度
書目名稱Genetic Counseling網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Genetic Counseling被引頻次
書目名稱Genetic Counseling被引頻次學(xué)科排名
書目名稱Genetic Counseling年度引用
書目名稱Genetic Counseling年度引用學(xué)科排名
書目名稱Genetic Counseling讀者反饋
書目名稱Genetic Counseling讀者反饋學(xué)科排名
作者: 膽小鬼 時(shí)間: 2025-3-21 21:52 作者: 憂傷 時(shí)間: 2025-3-22 01:21
0073-1595 on that the general practitioner (or specialist in any other field of medicine) cannot possibly give proper genetic counsel to his patients. Because he is not a genetics expert, he should, without exception, refer all such cases to the geneticist. This point of view would condemn this guide as potentially mor978-1-4615-9986-9Series ISSN 0073-1595 作者: 建筑師 時(shí)間: 2025-3-22 08:12 作者: MEEK 時(shí)間: 2025-3-22 10:22
https://doi.org/10.1007/978-3-642-79632-6ver any further cases in the proband’s family; of particular importance is the fact that there is nothing wrong with either of his parents. In situations of this kind, one of four explanations usually applies:作者: 脫水 時(shí)間: 2025-3-22 14:02
https://doi.org/10.1007/978-3-030-40006-4. But, as with lightning, some houses are, for very definite reasons, more endangered than others, and it is the business of the doctor to eliminate the possibility of such reasons or to evaluate them correctly where they do exist. Reassurance on any other grounds would be negligent, not to say irresponsible.作者: 脫水 時(shí)間: 2025-3-22 21:04
New Mutations and Phenocopies,ver any further cases in the proband’s family; of particular importance is the fact that there is nothing wrong with either of his parents. In situations of this kind, one of four explanations usually applies:作者: Sedative 時(shí)間: 2025-3-22 21:18
Malformations Not Subject to a Simple Mode of Inheritance,. But, as with lightning, some houses are, for very definite reasons, more endangered than others, and it is the business of the doctor to eliminate the possibility of such reasons or to evaluate them correctly where they do exist. Reassurance on any other grounds would be negligent, not to say irresponsible.作者: milligram 時(shí)間: 2025-3-23 03:04
Textbook 19762nd editiony study the highly specialized genetic literature available. This book is an attempt to fill this void. We have made an effort to keep it as short and clear as possible and to limit it to the important and most frequent genetic abnor- malities. In particular, we have tried to take into consid- erati作者: 新奇 時(shí)間: 2025-3-23 08:51
Karl Ernst Wohlfarth-Bottermann,Ernst Zebeher genetic considerations. It simplifies matters for oneself and the potentially required geneticist if the pedigree is drawn up with the symbols in common usage, such as those given in Figs. 2.1a, b.作者: Figate 時(shí)間: 2025-3-23 10:55
The Prague Spring as a Social MovementChurch still requires that the couple obtain a special dispensation (usually granted nowadays). But the ecclesiastic laws are also based on other than biologic considerations. This becomes obvious when one realizes that the church also forbids marriages between “spiritual” relatives—i.e., god-father and god-child.作者: Counteract 時(shí)間: 2025-3-23 17:31 作者: 遍及 時(shí)間: 2025-3-23 19:04
The Genetic Prognosis for a Consanguinous Marriage,Church still requires that the couple obtain a special dispensation (usually granted nowadays). But the ecclesiastic laws are also based on other than biologic considerations. This becomes obvious when one realizes that the church also forbids marriages between “spiritual” relatives—i.e., god-father and god-child.作者: 防水 時(shí)間: 2025-3-23 22:31
Appearances Deceive,st chapter after they have carefully read the rest. We recommend Chapter 2 as the starting point and Chapter 1 as the conclusion for those readers who have had little or no previous contact with genetics.作者: buoyant 時(shí)間: 2025-3-24 03:13 作者: Obstacle 時(shí)間: 2025-3-24 07:45
Prenatal Diagnosis,acts that a practicing physician should know. The tests and the diagnosis itself will, in any case, be carried out by specialized laboratories [for methodological details, see Emery (1970); Dorfman (1972); ., Orig. Art. Ser. Vol. VII, (1971).]作者: agglomerate 時(shí)間: 2025-3-24 14:07
Other Diseases Without a Simple Mode of Inheritance,ic counsel, in the stricter sense, will usually be required only if a family manifests an unusual number of similar diseases and if the circumstances indicate the existence of a Mendelian mode of inheritance.作者: beta-carotene 時(shí)間: 2025-3-24 17:39 作者: patella 時(shí)間: 2025-3-24 22:17 作者: 廣大 時(shí)間: 2025-3-24 23:24
The Human Element,sonality, the education, and the individual requirements of the patients. Human beings cannot be reduced to scientific formulas and no amount of scientific fact will compensate for a lack of human contact.作者: 是突襲 時(shí)間: 2025-3-25 04:43 作者: 小隔間 時(shí)間: 2025-3-25 07:40 作者: custody 時(shí)間: 2025-3-25 13:15 作者: 得罪 時(shí)間: 2025-3-25 17:39 作者: Individual 時(shí)間: 2025-3-25 20:17
https://doi.org/10.1007/978-3-030-98271-3ic counsel, in the stricter sense, will usually be required only if a family manifests an unusual number of similar diseases and if the circumstances indicate the existence of a Mendelian mode of inheritance.作者: 清真寺 時(shí)間: 2025-3-26 04:12 作者: 紡織品 時(shí)間: 2025-3-26 04:36
,Havel — Power to the Powerless,s of a particular mutagen is not always possible on the basis of direct observational data in man. However, the results of experimental mutation research with mammals give us additional evidence of the effects of particular mutagens (Hollaender, 1971; Vogel .., 1969; Vogel and R?hrborn,1970).作者: Mawkish 時(shí)間: 2025-3-26 11:29 作者: 角斗士 時(shí)間: 2025-3-26 14:11
Cytoplasmastruktur in Pflanzenzellen, terms and concepts, the exact meanings of which are defined and explained in later chapters. Readers are advised not to despair but to reread the first chapter after they have carefully read the rest. We recommend Chapter 2 as the starting point and Chapter 1 as the conclusion for those readers who作者: 隨意 時(shí)間: 2025-3-26 18:26
Karl Ernst Wohlfarth-Bottermann,Ernst Zebeormation about the proband’s relatives even when the proband himself is clearly suffering from a genetic defect of which the mode of inheritance has, ostensibly, been established. In genetics, there is always the possibility that a particular family will prove to be an exception. It happens, for ins作者: 分解 時(shí)間: 2025-3-26 21:46 作者: outskirts 時(shí)間: 2025-3-27 03:40
https://doi.org/10.1007/978-3-642-79632-6to the autosomal-dominant mode of inheritance. Frequently, however, the symptoms of the proband will be identical to those observed in other families with the same anomaly in which the autosomal-dominant mode has been definitely established. Yet even the most painstaking research has failed to disco作者: seroma 時(shí)間: 2025-3-27 08:54 作者: Clumsy 時(shí)間: 2025-3-27 13:28
https://doi.org/10.1007/978-1-4684-6814-4nts of mongoloid children come for counseling and wish to know the risk involved in having further children. At the same time, this syndrome is an excellent example of a defect whose roots are so complex that no generally applicable formula for counseling can be given. It again illustrates how very 作者: Antagonist 時(shí)間: 2025-3-27 15:14
https://doi.org/10.1007/978-3-030-40006-4 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 correct answer作者: Watemelon 時(shí)間: 2025-3-27 18:27
https://doi.org/10.1057/9780230505629ield of research has been expanding rapidly in recent years. We will not discuss the highly technical details here but will confine ourselves to the facts that a practicing physician should know. The tests and the diagnosis itself will, in any case, be carried out by specialized laboratories [for me作者: 貴族 時(shí)間: 2025-3-27 22:15 作者: 雇傭兵 時(shí)間: 2025-3-28 03:32 作者: Nomogram 時(shí)間: 2025-3-28 07:35 作者: expound 時(shí)間: 2025-3-28 10:44
,Havel — Power to the Powerless,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作者: Magnificent 時(shí)間: 2025-3-28 17:04
https://doi.org/10.1057/9781137317476t be used, if at all avoidable, to treat illnesses during the first 3 to 4 months of a pregnancy. The most dangerous known chemical teratogen for an embryo, thalidomide, is no longer used therapeutically. A warning is therefore redundant.作者: glomeruli 時(shí)間: 2025-3-28 21:41 作者: 領(lǐng)巾 時(shí)間: 2025-3-28 23:37
https://doi.org/10.1007/978-1-4615-9986-9Mutation; chromosome; counseling; genetics; medicine; mutagen; patients; prenatal diagnosis作者: 在前面 時(shí)間: 2025-3-29 04:53
Alice Schofield,Ora Bernard Ph.Dmutations, the autosomal recessive mode presents one with the progeny of ostensibly normal parents who are heterozygous for the gene in question; i.e., they carry only one defective gene and the normal allele with its “healthy” information prevents the defect from manifesting itself. Figure 5.1 is a diagram of the typical situation.作者: LUCY 時(shí)間: 2025-3-29 09:37 作者: 北極人 時(shí)間: 2025-3-29 12:02 作者: justify 時(shí)間: 2025-3-29 17:44 作者: 臭了生氣 時(shí)間: 2025-3-29 22:30 作者: DEAF 時(shí)間: 2025-3-30 03:38
Genetic Counseling978-1-4615-9986-9Series ISSN 0073-1595 作者: 慌張 時(shí)間: 2025-3-30 05:20 作者: zonules 時(shí)間: 2025-3-30 12:00 作者: 治愈 時(shí)間: 2025-3-30 13:00 作者: effrontery 時(shí)間: 2025-3-30 19:05
Recording a Family Medical History or Pedigree,ormation about the proband’s relatives even when the proband himself is clearly suffering from a genetic defect of which the mode of inheritance has, ostensibly, been established. In genetics, there is always the possibility that a particular family will prove to be an exception. It happens, for ins作者: Impugn 時(shí)間: 2025-3-31 00:18 作者: PET-scan 時(shí)間: 2025-3-31 02:20
New Mutations and Phenocopies,to the autosomal-dominant mode of inheritance. Frequently, however, the symptoms of the proband will be identical to those observed in other families with the same anomaly in which the autosomal-dominant mode has been definitely established. Yet even the most painstaking research has failed to disco作者: Brain-Imaging 時(shí)間: 2025-3-31 05:53
The Autosomal Recessive Mode of Inheritance and Tests for the Detection of Heterozygotes,mutations, the autosomal recessive mode presents one with the progeny of ostensibly normal parents who are heterozygous for the gene in question; i.e., they carry only one defective gene and the normal allele with its “healthy” information prevents the defect from manifesting itself. Figure 5.1 is a
