COLOUR VISION DEFICIENCY IN ONE OF 2 PRESUMABLY MONOZYGOTIC TWINS WITH SECONDARY AMENORRHOEA

被引：16

作者：

PHILIP, J

ANDERSEN, CH

DREYER, V

FREIESLEBEN, E

GURTLER, H

HAUGE, M

KISSMEYE.F

NIELSEN, LS

PERS, M

ROBSON, EB

SVEJGAARD, A

SORENSEN, B

机构：

[1] Chromosome Laboratory, Department of Obstetrics and Gynaecology A-I, Clinic of Aviation Ophthalmology, Blood-Bank, Department of Plastic Surgery, Rigshospitalet, University of Copenhagen

[2] Department of Anthropology, Institute of Forensic Medicine, Institute of Human Genetics, University of Copenhagen

[3] Medical Research Council Human Biochemical Genetics Unit, University College London

[4] Blood-Bank and Blood Grouping Laboratory, University Hospital, Aarhus

来源：

ANNALS OF HUMAN GENETICS | 1969年 / 33卷

关键词：

D O I：

10.1111/j.1469-1809.1969.tb01644.x

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

[No abstract available]

引用

页码：185 / +

页数：1