Frequency of satelliting of the human chromosomes 21 and 22 and the identity of the mongol chromosome.
作者信息
Ford E H, Woollam D H
出版信息
Lancet. 1968 Feb 17;1(7538):327-8. doi: 10.1016/s0140-6736(68)90793-9.
PMID:4170160
Abstract
摘要
相似文献
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Frequency of satelliting of the human chromosomes 21 and 22 and the identity of the mongol chromosome.人类21号和22号染色体随体出现的频率以及先天愚型染色体的特性
Lancet. 1968 Feb 17;1(7538):327-8. doi: 10.1016/s0140-6736(68)90793-9.
2
Origin of extra chromosome in trisomy 21.21三体综合征中额外染色体的起源。
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[Dermatoglyphics of the palms and fingers in Down's syndrome with partial trisomy of chromosome 21].[21号染色体部分三体性唐氏综合征患者手掌和手指的皮纹学研究]
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A giant short arm of no. 21 chromosome in mother of 21/21 translocation mongol.21/21易位型先天愚型患儿母亲第21号染色体长臂缺失。
J Med Genet. 1976 Oct;13(5):411-2. doi: 10.1136/jmg.13.5.411.
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Letter: Mongolism by tertiary trisomy.信件：三体性导致的先天愚型
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[Problems in chromosome studies in Down's syndrome].[唐氏综合征染色体研究中的问题]
Saishin Igaku. 1968 Feb 10;24(2):306.
8
A boy with trisomic Down's syndrome and a familial 5-?7 translocation, 47,XY,+21, t (5q-; ?7p+).一名患有三体性唐氏综合征且伴有家族性5;7易位的男孩，核型为47,XY,+21,t(5q-;7p+) 。
Jinrui Idengaku Zasshi. 1972 Sep;17(1):38-43.
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Trisomy-21 in mother and child. Report of a case.母婴21三体综合征。病例报告。
Obstet Gynecol. 1970 Nov;36(5):731-4.
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Chromosome anomalies in mongolism.先天愚型中的染色体异常。
N Engl J Med. 1968 Mar 7;278(10):565-6. doi: 10.1056/NEJM196803072781021.
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Variations in karyotypes of normal premature babies, new-born babies and infants.正常早产儿、新生儿和婴儿的核型变异。
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Nucleoli of cultured human lymphocytes. II. Nuceolar fusion and its relation to acrocentric association.培养的人淋巴细胞的核仁。II. 核仁融合及其与近端着丝粒联合的关系。
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