HISTORICAL STUDY - DELANGE,CORNELIA,C. (1871-1950) - A PIONEER IN CLINICAL GENETICS

被引:5
作者
DEKNECHTVANEEKELEN, A
HENNEKAM, RCM
机构
[1] UNIV AMSTERDAM,ACAD MED CTR,DEPT PEDIAT,1105 AZ AMSTERDAM,NETHERLANDS
[2] UNIV AMSTERDAM,ACAD MED CTR,INST HUMAN GENET,1105 AZ AMSTERDAM,NETHERLANDS
[3] FREE UNIV AMSTERDAM,FAC MED,MED HIST SECT,AMSTERDAM,NETHERLANDS
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1994年 / 52卷 / 03期
关键词
HISTORY; CLINICAL GENETICS IN THE NETHERLANDS; BRACHMANN-DE LANGE SYNDROME;
D O I
10.1002/ajmg.1320520302
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The life and work in the field of clinical genetics of one of the most outstanding Dutch pediatricians of the first half of the twentieth century, Cornelia C. de Lange (1871-1950), is described against the background of the development of pediatrics, anthropogenetics, and clinical genetics in the Netherlands. Cornelia de Lange specialized in and worked on all aspects of the broad field of pediatrics. During her 50 years of practice she collected an immense series of observations on pediatric disorders. As theories on human genetics developed during the 1920s and 1930s, her interest in congenital disorders and heredity increased as she saw the implications for the pediatric clinic. She benefitted from her vast experience and her knowledge of the national and international literature when she recognised and described new entities, one of which is named after her: the Brachmann-De Lange syndrome. (C) 1994 Wiley-Liss, Inc.
引用
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页码:257 / 266
页数:10
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