標(biāo)題: Titlebook: Genetic Disorders of the Indian Subcontinent; Dhavendra Kumar Book 2004 Springer Science+Business Media New York 2004 Chromosom.developing [打印本頁(yè)] 作者: emanate 時(shí)間: 2025-3-21 18:46
書目名稱Genetic Disorders of the Indian Subcontinent影響因子(影響力)
書目名稱Genetic Disorders of the Indian Subcontinent影響因子(影響力)學(xué)科排名
書目名稱Genetic Disorders of the Indian Subcontinent網(wǎng)絡(luò)公開度
書目名稱Genetic Disorders of the Indian Subcontinent網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Genetic Disorders of the Indian Subcontinent被引頻次
書目名稱Genetic Disorders of the Indian Subcontinent被引頻次學(xué)科排名
書目名稱Genetic Disorders of the Indian Subcontinent年度引用
書目名稱Genetic Disorders of the Indian Subcontinent年度引用學(xué)科排名
書目名稱Genetic Disorders of the Indian Subcontinent讀者反饋
書目名稱Genetic Disorders of the Indian Subcontinent讀者反饋學(xué)科排名
作者: 精確 時(shí)間: 2025-3-21 20:18 作者: Ingenuity 時(shí)間: 2025-3-22 00:43 作者: 向下 時(shí)間: 2025-3-22 05:59
Epidemiology of Genetic Diseasess is 67, 84, 17, and 51, respectively (State of the World’s Children, 2003). In all these countries there is an accelerating demographic switch to non-communicable diseases, particularly among the urban populations (Verma and Bijarnia, 2002). This is most apparent in Sri Lanka with its low mortality作者: lethal 時(shí)間: 2025-3-22 09:47
Immunogenetic Basis of Variation and Disease Susceptibilityble impact on developing new perspectives in molecular medicine. An understanding of the genetic basis of complex, multi-factorial diseases is crucial for identifying predisposing factors, assessing the effect of gene-environment interactions, predicting individual response to specific drugs and dis作者: 甜瓜 時(shí)間: 2025-3-22 15:09
Consanguinity: Cultural, Religious and Social Aspects (Bittles, 1994). At a biological level, consanguineous unions may increase the risk in the homozygous state in their children [note 1] (Modell and Darr, 2003). This might be reflected in relatively higher probability of an autosomal recessive inherited disease and certain types of congenital malfor作者: 甜瓜 時(shí)間: 2025-3-22 18:31
Congenital Developmental Anomaliesr about 3% of all children born in any hospital or in any country will have a significant congenital abnormality. It may be more than of cosmetic concern and which, if uncorrected, will interfere with normal functioning (Aase, 1990). Such anomalies occur in only a small fraction of all new born. How作者: Diluge 時(shí)間: 2025-3-22 21:50
Malformation Syndromes in India multiple malformation syndromes associated with subtle dysmorphism and minor malformations may not become clinically relevant till later part of infancy or childhood when associated with developmental delay or mental retardation. Hence, incidence of multiple malformation syndromes obtained from exa作者: chlorosis 時(shí)間: 2025-3-23 05:01
Down Syndrome In Indiaenetics because, until then, human diploid constitution was believed to be 48. The impact of this discovery was soon felt in medical cytogenetics, when Lejeune et al (1959) reported that the common mental retardation disorder, Down syndrome [DS] was caused by trisomy of one of the G-group chromosome作者: 免費(fèi) 時(shí)間: 2025-3-23 07:42 作者: indenture 時(shí)間: 2025-3-23 13:04 作者: obeisance 時(shí)間: 2025-3-23 16:26 作者: Robust 時(shí)間: 2025-3-23 20:09
Thalassaemias and Other Haemoglobinopathiesof the thalassaemias, characterised by either the reduced synthesis of one or more of the globin chains, and the haemoglobin variants, characterised by the synthesis of a structurally abnormal globin (Weatherall and Clegg, 2001). They form the most common single gene disorder in the world, and are f作者: Asymptomatic 時(shí)間: 2025-3-23 22:19
Disorders of Haemostasis and Thrombosisred for, in developing countries, where data on incidence is limited (Nathwani and Tuddenham, 1992). Some haemostasis and thrombosis centres in the UK serve populations with large south Asian groups. The nature and incidence of haemostasis disorder seen in these groups will partly reflect those in t作者: Negotiate 時(shí)間: 2025-3-24 06:14
Glucose-6-Phosphate Dehydrogenase Deficiency and Other Inherited Red Cell Defects discussed elsewhere in this volume. The remainder, due either to the inadequate activity of one or other red cell enzyme or to a defect in the red cell cytoskeleton, are discussed in this chapter. Glucose-6-phosphate dehydrogenase (G6PD) deficiency is by far the most important disorder in this grou作者: 不溶解 時(shí)間: 2025-3-24 09:00 作者: 苦澀 時(shí)間: 2025-3-24 11:38
Inherited Skeletal Dysplasias and Collagen Diseasesg with limb abnormalities and disproportionate short stature. There are over 100 distinct skeletal dysplasias, which have been classified primarily on the basis of the clinical or radiographic characteristics (International Working Group, 1998). The management of these conditions require a combined 作者: 血友病 時(shí)間: 2025-3-24 18:01 作者: 雄辯 時(shí)間: 2025-3-24 21:19
Genetics Diseases of the Eye in Indiacs’. It was through ophthalmology that some fundamental issues were recognized and understood in genetics. One of the genetic diseases identified very early in human history, in 1796, was protanopia (color blindness). The first genetic disease to be mapped was color vision deficiency to X-chromosome作者: 效果 時(shí)間: 2025-3-25 01:30
Book 2004ethnic groups and its distinct religious, cultural and social characteristics. Like many developing countries in Asia, it is passing through both demographic and epidemiological transitions whereby, at least in some parts, the diseases of severe poverty are being replaced by those of Westemisation; 作者: deciduous 時(shí)間: 2025-3-25 06:31 作者: indoctrinate 時(shí)間: 2025-3-25 08:37 作者: GRUEL 時(shí)間: 2025-3-25 12:49 作者: slipped-disk 時(shí)間: 2025-3-25 19:16 作者: 生來(lái) 時(shí)間: 2025-3-25 21:37 作者: 粘連 時(shí)間: 2025-3-26 03:30
Thalassaemias and Other Haemoglobinopathiesnd prenatal diagnosis (Petrou and Modell, 1995). The most important disorders for which prenatal diagnosis is considered are β°-thalassaemia, ?-thalassaemia, sickle cell anaemia and the various compound heterozygous states that result in a clinically significant disease.作者: integrated 時(shí)間: 2025-3-26 07:41
Disorders of Haemostasis and Thrombosis serve populations with large south Asian groups. The nature and incidence of haemostasis disorder seen in these groups will partly reflect those in the country of origin but other factors, such as the degree of consanguinity, may also be important.作者: indices 時(shí)間: 2025-3-26 11:19 作者: Abominate 時(shí)間: 2025-3-26 12:40 作者: 有罪 時(shí)間: 2025-3-26 18:30 作者: 逢迎白雪 時(shí)間: 2025-3-27 00:16 作者: MURAL 時(shí)間: 2025-3-27 01:32
Self-Interacting Cold Dark Matter Halosome and Klinefelter syndrome (Ford et al., 1959; Jacobs and Strong, 1959) were caused by the loss (45,XO) and gain (47,XXY) of the X-chromosome, respectively. These examples highlight the importance of establishing the correct diploid number in man.作者: neoplasm 時(shí)間: 2025-3-27 08:16 作者: Euthyroid 時(shí)間: 2025-3-27 09:28 作者: immunity 時(shí)間: 2025-3-27 15:42
The Indian Subcontinent and Human Genetics: An Introductionfor example ‘. etc. The Indian subcontinent is one of the largest geo-political regions of the Asian continent. The geographic and political boundaries include India, Pakistan, Bangladesh, Sri Lanka, Nepal, Bhutan and other small islands of the Indian Ocean. There is marked cultural and ethnic diversity with considerable overlap.作者: 背書 時(shí)間: 2025-3-27 19:23
Genomic and Gene Diversity among the People of the Indian Subcontinent (50,000–20,000 BC), humans had spread to many parts of the Indian subcontinent. Neolithic (7,000–5,000 BC) settlements are numerous, and it appears that Austric languages are descended from the Neolithic peoples.作者: HUMP 時(shí)間: 2025-3-27 22:42 作者: 尖牙 時(shí)間: 2025-3-28 03:42 作者: Allure 時(shí)間: 2025-3-28 06:31 作者: 法律 時(shí)間: 2025-3-28 10:38 作者: 對(duì)待 時(shí)間: 2025-3-28 15:43 作者: 松緊帶 時(shí)間: 2025-3-28 18:49
Anatomie, Entwicklung und Fehlbildungen the basis of the clinical or radiographic characteristics (International Working Group, 1998). The management of these conditions require a combined effort involving various specialists including radiologists, orthopaedic surgeons, clinical geneticists, physiotherapists, rehabilitation clinicians and clinical psychologists.作者: 品牌 時(shí)間: 2025-3-29 00:35
https://doi.org/10.1007/978-3-7091-4812-9avis and Hind, 1999).These problems may be exacerbated in developing countries where poor nutrition and/or limited access to educational and medical facilities, coupled with increased reliance on verbal communication skills, can result in social isolation and reduced occupational opportunities (Kumar, 1997; Elahi et al., 1998).作者: 故意釣到白楊 時(shí)間: 2025-3-29 05:19
https://doi.org/10.1007/978-1-349-19982-2 rate, and it is not surprising, therefore, that non-communicable diseases of adults are receiving great attention in this country. In all the four countries, a gradually increasing prevalence of complex diseases due to mutifactorial/ polygenic inheritance, such as diabetes mellitus, coronary artery disease, hypertension etc., has been recorded.作者: QUAIL 時(shí)間: 2025-3-29 10:59
The Lower End of the Main Sequencemations. However consanguinity does not increase the risk of autosomal dominant or X-linked disorders. Studies on consanguinity have focussed on the probable higher risk of prenatal or postnatal mortality and/or morbidity due to congenital malformations and/or intellectual disability (Bundey and Aslam, 1993) [note 2].作者: 召集 時(shí)間: 2025-3-29 11:27
The Birth of the Southern Question,p, both because of its high incidence in subjects from the Indian sub-continent and because of its clinical manifestations. This brief review will concentrate on the clinical and laboratory aspects of intrinsic red cell defects, with an emphasis on G6PD deficiency.作者: 殘暴 時(shí)間: 2025-3-29 18:54 作者: 獸群 時(shí)間: 2025-3-29 21:16 作者: tenosynovitis 時(shí)間: 2025-3-30 01:31
Glucose-6-Phosphate Dehydrogenase Deficiency and Other Inherited Red Cell Defectsp, both because of its high incidence in subjects from the Indian sub-continent and because of its clinical manifestations. This brief review will concentrate on the clinical and laboratory aspects of intrinsic red cell defects, with an emphasis on G6PD deficiency.作者: LAP 時(shí)間: 2025-3-30 04:33
Immunogenetic Basis of Variation and Disease Susceptibilityypes, makes it a good marker system for exploring disease predisposing genes. Such a polymorphism could also provide a genetic basis for the observed inter-population and inter-individual variation in immune responsiveness and resultant disease susceptibility/resistance profiles. In this context, th作者: outset 時(shí)間: 2025-3-30 11:11 作者: 衰弱的心 時(shí)間: 2025-3-30 13:40
Malformation Syndromes in India syndromes and diagnostic facilities were scarce. The authors observed that that recording of multiple malformations was inadequate as in most of the cases only the major malformation was recorded and the associated minor defects were not mentioned.作者: Affectation 時(shí)間: 2025-3-30 20:29 作者: Ingenuity 時(shí)間: 2025-3-30 23:28
Book 2004been done towards tracing the origins of its different ethnic groups. In the current excitement generated by the human genome project and the molecular and genetic approach to the study of human disease, there is little doubt that this field will develop and flourish in India in the future. Although作者: 葡萄糖 時(shí)間: 2025-3-31 03:35
https://doi.org/10.1007/978-1-349-10651-6ypes, makes it a good marker system for exploring disease predisposing genes. Such a polymorphism could also provide a genetic basis for the observed inter-population and inter-individual variation in immune responsiveness and resultant disease susceptibility/resistance profiles. In this context, th作者: fastness 時(shí)間: 2025-3-31 05:13 作者: wall-stress 時(shí)間: 2025-3-31 09:48
Dark Humor in Films of the 1960s, syndromes and diagnostic facilities were scarce. The authors observed that that recording of multiple malformations was inadequate as in most of the cases only the major malformation was recorded and the associated minor defects were not mentioned.作者: DOLT 時(shí)間: 2025-3-31 16:31 作者: EWE 時(shí)間: 2025-3-31 20:42 作者: artifice 時(shí)間: 2025-3-31 22:47 作者: 珠寶 時(shí)間: 2025-4-1 03:13 作者: 火海 時(shí)間: 2025-4-1 07:32
Turgut ?zal and the Gates of Desires is like a jigsaw puzzle with many missing pieces. However, there is enough anthropological and archaeological evidence to show that from time immemorial people of many different ethnic stocks, cultures and languages have inhabited India and contributed to the present day gene pool of the subcontin作者: Foreknowledge 時(shí)間: 2025-4-1 11:45 作者: aqueduct 時(shí)間: 2025-4-1 14:38
https://doi.org/10.1007/978-1-349-10651-6ble impact on developing new perspectives in molecular medicine. An understanding of the genetic basis of complex, multi-factorial diseases is crucial for identifying predisposing factors, assessing the effect of gene-environment interactions, predicting individual response to specific drugs and dis
