找回密碼
 To register

QQ登錄

只需一步,快速開始

掃一掃,訪問微社區(qū)

打印 上一主題 下一主題

Titlebook: Genetic Disorders of the Indian Subcontinent; Dhavendra Kumar Book 2004 Springer Science+Business Media New York 2004 Chromosom.developing

[復(fù)制鏈接]
樓主: emanate
11#
發(fā)表于 2025-3-23 13:04:15 | 只看該作者
12#
發(fā)表于 2025-3-23 16:26:28 | 只看該作者
13#
發(fā)表于 2025-3-23 20:09:19 | 只看該作者
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
14#
發(fā)表于 2025-3-23 22:19:11 | 只看該作者
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
15#
發(fā)表于 2025-3-24 06:14:06 | 只看該作者
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
16#
發(fā)表于 2025-3-24 09:00:34 | 只看該作者
17#
發(fā)表于 2025-3-24 11:38:26 | 只看該作者
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
18#
發(fā)表于 2025-3-24 18:01:44 | 只看該作者
19#
發(fā)表于 2025-3-24 21:19:47 | 只看該作者
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
20#
發(fā)表于 2025-3-25 01:30:37 | 只看該作者
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;
 關(guān)于派博傳思  派博傳思旗下網(wǎng)站  友情鏈接
派博傳思介紹 公司地理位置 論文服務(wù)流程 影響因子官網(wǎng) 吾愛論文網(wǎng) 大講堂 北京大學(xué) Oxford Uni. Harvard Uni.
發(fā)展歷史沿革 期刊點評 投稿經(jīng)驗總結(jié) SCIENCEGARD IMPACTFACTOR 派博系數(shù) 清華大學(xué) Yale Uni. Stanford Uni.
QQ|Archiver|手機版|小黑屋| 派博傳思國際 ( 京公網(wǎng)安備110108008328) GMT+8, 2025-10-10 04:56
Copyright © 2001-2015 派博傳思   京公網(wǎng)安備110108008328 版權(quán)所有 All rights reserved
快速回復(fù) 返回頂部 返回列表
滁州市| 沁水县| 开鲁县| 南城县| 镇康县| 东乡族自治县| 宝坻区| 莱阳市| 黑龙江省| 建阳市| 台湾省| 灯塔市| 宜兰市| 翁牛特旗| 双鸭山市| 兰西县| 靖边县| 上高县| 射洪县| 肃宁县| 长丰县| 吴忠市| 开原市| 中方县| 营口市| 海阳市| 福州市| 蒙山县| 安西县| 汪清县| 卢龙县| 巨鹿县| 卓资县| 苍南县| 来安县| 宜都市| 邓州市| 蚌埠市| 东阿县| 山丹县| 沿河|