標(biāo)題: Titlebook: Genetic Disorders, Syndromology and Prenatal Diagnosis; T. V. N. Persaud Book 1982 MTP Press Limited 1982 development.embryo.embryology.ep [打印本頁] 作者: 兩邊在擴(kuò)散 時(shí)間: 2025-3-21 17:28
書目名稱Genetic Disorders, Syndromology and Prenatal Diagnosis影響因子(影響力)
書目名稱Genetic Disorders, Syndromology and Prenatal Diagnosis影響因子(影響力)學(xué)科排名
書目名稱Genetic Disorders, Syndromology and Prenatal Diagnosis網(wǎng)絡(luò)公開度
書目名稱Genetic Disorders, Syndromology and Prenatal Diagnosis網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Genetic Disorders, Syndromology and Prenatal Diagnosis被引頻次
書目名稱Genetic Disorders, Syndromology and Prenatal Diagnosis被引頻次學(xué)科排名
書目名稱Genetic Disorders, Syndromology and Prenatal Diagnosis年度引用
書目名稱Genetic Disorders, Syndromology and Prenatal Diagnosis年度引用學(xué)科排名
書目名稱Genetic Disorders, Syndromology and Prenatal Diagnosis讀者反饋
書目名稱Genetic Disorders, Syndromology and Prenatal Diagnosis讀者反饋學(xué)科排名
作者: NUDGE 時(shí)間: 2025-3-21 20:33
Zugeordnete Normalprojektionen,The cytogenetics of several recessive inheritance disease states in human will be discussed. These diseases belong to the categories of (1) autosomal recessive and (2) X-linked recessive disorders.作者: HEAVY 時(shí)間: 2025-3-22 02:32
Helmut Winterhager,Hans-Peter KrugThe process of syndrome delineation can be divided into the following stages:作者: 內(nèi)部 時(shí)間: 2025-3-22 08:30 作者: 全部 時(shí)間: 2025-3-22 11:01
Chromosomal abnormalities in single gene disorders,The cytogenetics of several recessive inheritance disease states in human will be discussed. These diseases belong to the categories of (1) autosomal recessive and (2) X-linked recessive disorders.作者: irreducible 時(shí)間: 2025-3-22 15:53 作者: irreducible 時(shí)間: 2025-3-22 20:41
Prenatal diagnosis of genetic diseases by amniocentesis,Prenatal diagnosis is now possible for a considerable number of genetic diseases and/or birth defects using a variety of techniques.作者: 無法取消 時(shí)間: 2025-3-23 00:03
https://doi.org/10.1007/978-3-662-30331-3chromatic regions, especially the short arm and satellite regions of the acrocentric chromosomes and the long arm of the Y chromosome. The advent of new staining techniques has helped in the identification of sites of morphological variation in human chromosomes. The variable segments correspond to 作者: POINT 時(shí)間: 2025-3-23 01:25
Maria Lipp,Karl-Heinz Maria Tillwichabnormal development of the aborted conceptus in these cases has been well documented since the time of Mall in 1908. who also observed that the frequency of anomalies is directly proportional to the developmental age of the conceptus. In the aborted embryo the incidence is over 80%, declining throu作者: temperate 時(shí)間: 2025-3-23 07:52 作者: 瘋狂 時(shí)間: 2025-3-23 11:07
Umkehrungen des Abelschen Stetigkeitssatzes,ion of the body sex (also referred to as ‘secondary sex determination’) or has been considered from one point of view, e.g. chromosomal. It is therefore essential to define sex determination as the complex of molecular (nucleic acids and their products), cellular and histological events which combin作者: 箴言 時(shí)間: 2025-3-23 17:25 作者: Amorous 時(shí)間: 2025-3-23 20:15
Hans-Jürgen Zimmermann,Hubert V?lzgenrn cytogenetic surveys over the past two decades. Such surveys were conducted either through examination of the chromosomes of the peripheral blood leukocytes, or through examination of X- and/or Y-chromatin from the amnion or from the cells of buccal mucosa, followed by karyotyping those children f作者: AMEND 時(shí)間: 2025-3-24 01:37
Reimar Pohlman,Gerhard Grieshammer non-fierce, but increasing knowledge especially of biological systems made the development of more complex classifications methods a necessity. Taxonomy has been defined as ‘the theoretical study of classification including its bases, principles, procedures and rules’. and numerical taxonomy refers作者: MEAN 時(shí)間: 2025-3-24 03:30 作者: 生意行為 時(shí)間: 2025-3-24 07:13
Die Apperzeption im kindlichen Denken,of sexual differentiation. We present information on the recent developments and current knowledge regarding congenital adrenal hyperplasia (CAH), the most common cause of ambiguous genitalia in the newborn.作者: ARENA 時(shí)間: 2025-3-24 10:55 作者: NATAL 時(shí)間: 2025-3-24 17:56 作者: 值得 時(shí)間: 2025-3-24 19:05
Maria Lipp,Gunhild Frielingsdorf the detection of human chromosome polymorphism are the QFQ (Q-bands by fluorescence using quinacrine), the CBG (C-bands by barium hydroxide staining with Giemsa), RFA (R-bands by fluorescence using acridine orange), and the silver staining. for the nucleolar organizer regions (NOR) of acrocentric chromosomes.作者: bacteria 時(shí)間: 2025-3-25 00:52 作者: 合唱隊(duì) 時(shí)間: 2025-3-25 04:11 作者: 大范圍流行 時(shí)間: 2025-3-25 09:30
Current concepts in congenital adrenal hyperplasia,of sexual differentiation. We present information on the recent developments and current knowledge regarding congenital adrenal hyperplasia (CAH), the most common cause of ambiguous genitalia in the newborn.作者: 不可侵犯 時(shí)間: 2025-3-25 14:50
978-94-011-6671-3MTP Press Limited 1982作者: abstemious 時(shí)間: 2025-3-25 16:24 作者: ASSAY 時(shí)間: 2025-3-25 22:03
Hans-Jürgen Zimmermann,Hubert V?lzgenound to present chromatin anomalies. The first method was used in ?rhus, Denmark., Northeastern, USA., Scotland., Tokyo, Japan. and the collaborative study in the USA.. The Denver., Edinburgh. and Toronto. studies carried instead sex chromatin surveys.作者: 難管 時(shí)間: 2025-3-26 02:34
Gegenstand: Der Emotionsbegriff,knowledge of how the body parts develop normally and inferences drawn from embryolog-ical experiments on animal models which provide clues that can be used to explain how the developing tissues interact.作者: TOM 時(shí)間: 2025-3-26 08:09 作者: 拋射物 時(shí)間: 2025-3-26 08:28 作者: Derogate 時(shí)間: 2025-3-26 16:39 作者: SEED 時(shí)間: 2025-3-26 18:29
Reimar Pohlman,Gerhard Grieshammerhe medical sciences have started to adapt and use numerical taxonomy techniques. However, there is now increasing awareness of their value as an objective tool in studying patients, syndromes and disease entities.作者: 糾纏,纏繞 時(shí)間: 2025-3-26 23:34 作者: 形狀 時(shí)間: 2025-3-27 01:30
Book 1982ined far less than those for other causes of death, such as infectious and nutritional diseases. As many as 50 % of all pregnancies terminate as miscarriages, and in the majority of cases this is the result of faulty intrauterine development. Major congenital malformations are present in at least 2 作者: indenture 時(shí)間: 2025-3-27 07:39
have declined far less than those for other causes of death, such as infectious and nutritional diseases. As many as 50 % of all pregnancies terminate as miscarriages, and in the majority of cases this is the result of faulty intrauterine development. Major congenital malformations are present in a作者: Exaggerate 時(shí)間: 2025-3-27 10:30 作者: inspired 時(shí)間: 2025-3-27 16:14 作者: Synthesize 時(shí)間: 2025-3-27 21:26
The role of chromosome heteromorphism in developmental anomalies,chromatic regions, especially the short arm and satellite regions of the acrocentric chromosomes and the long arm of the Y chromosome. The advent of new staining techniques has helped in the identification of sites of morphological variation in human chromosomes. The variable segments correspond to 作者: 沉著 時(shí)間: 2025-3-28 00:51
Embryonic development in patients with a high risk of early pregnancy loss,abnormal development of the aborted conceptus in these cases has been well documented since the time of Mall in 1908. who also observed that the frequency of anomalies is directly proportional to the developmental age of the conceptus. In the aborted embryo the incidence is over 80%, declining throu作者: CAND 時(shí)間: 2025-3-28 05:53
Human chromosome polymorphism and congenital defects, the detection of human chromosome polymorphism are the QFQ (Q-bands by fluorescence using quinacrine), the CBG (C-bands by barium hydroxide staining with Giemsa), RFA (R-bands by fluorescence using acridine orange), and the silver staining. for the nucleolar organizer regions (NOR) of acrocentric c作者: 商業(yè)上 時(shí)間: 2025-3-28 09:54
H-Y antigen and the aetiology of genetic disorders in sex determination,ion of the body sex (also referred to as ‘secondary sex determination’) or has been considered from one point of view, e.g. chromosomal. It is therefore essential to define sex determination as the complex of molecular (nucleic acids and their products), cellular and histological events which combin作者: 微粒 時(shí)間: 2025-3-28 12:36
Effect of chromosome changes on body and mind development,hodology of study was described and the correct chromosome number of our species established. The new techniques that developed soon afterwards opened a whole new field in human biology, in relation to both normal and abnormal variation. Up to 1970 several new syndromes had been delineated, the aeti作者: 制定法律 時(shí)間: 2025-3-28 17:06 作者: intention 時(shí)間: 2025-3-28 20:24
Numerical taxonomy in the study of birth defects, non-fierce, but increasing knowledge especially of biological systems made the development of more complex classifications methods a necessity. Taxonomy has been defined as ‘the theoretical study of classification including its bases, principles, procedures and rules’. and numerical taxonomy refers作者: 法官 時(shí)間: 2025-3-29 01:53 作者: Psychogenic 時(shí)間: 2025-3-29 06:52
Current concepts in congenital adrenal hyperplasia,of sexual differentiation. We present information on the recent developments and current knowledge regarding congenital adrenal hyperplasia (CAH), the most common cause of ambiguous genitalia in the newborn.作者: Melanocytes 時(shí)間: 2025-3-29 09:28 作者: 享樂主義者 時(shí)間: 2025-3-29 15:22
Congenital anomalies: the role of ultrasound,have resulted in a progressive and dramatic fall in perinatal mortality; for example, as observed in Manitoba, the perinatal mortality rate has fallen from 25 per 1000 in 1976 to a current figure of 14.3 per 1000 in 1979.. Major life-threatening congenital anomalies occur in approximately 1 % of all作者: 重畫只能放棄 時(shí)間: 2025-3-29 19:24 作者: 按時(shí)間順序 時(shí)間: 2025-3-29 22:19 作者: 表示問 時(shí)間: 2025-3-30 03:18 作者: Bravado 時(shí)間: 2025-3-30 08:02
Embryonic development in patients with a high risk of early pregnancy loss,s for subsequent counselling and management of the patient. It is as a result of the work done in the 1960s by the research groups led by Carr., Boué., Shepard., Nishimura., and their associates that the detailed diagnostic study of abortuses is gradually becoming an accepted part of the work of a s作者: expository 時(shí)間: 2025-3-30 09:17 作者: 多山 時(shí)間: 2025-3-30 14:28
Congenital anomalies: the role of ultrasound,g perinatal mortality. Obstetricians pay a price for this aggressive approach and nowhere is it more apparent than when maternal morbidity occurs as a result of aggressive treatment for the infant with unrecognized lethal congenital anomalies. Developing in parallel with this new obstetric dilemma a作者: osculate 時(shí)間: 2025-3-30 19:46
https://doi.org/10.1007/978-3-662-30331-3ant’ has been recommended (Paris Conference, 1971).. The supplement to the Paris Conference (1975). subsequently advocated the term ‘heteromorphism’ to be used in describing situations where deviations from the norm of chromosome morphology are observed. Besides conventional staining, the most frequ作者: HATCH 時(shí)間: 2025-3-30 20:51 作者: 沙發(fā) 時(shí)間: 2025-3-31 04:07 作者: 溫和女人 時(shí)間: 2025-3-31 07:22
