A boy with trisomic Down's syndrome and a familial 5-?7 translocation, 47,XY,+21, t (5q-; ?7p+).
作者信息
Yanagisawa S
出版信息
Jinrui Idengaku Zasshi. 1972 Sep;17(1):38-43.
PMID:4265909
Abstract
摘要
相似文献
1
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.
2
3
[Familial pericentric inversion of y chromosome and Down's syndrome].[Y染色体家族性臂间倒位与唐氏综合征]
An Esp Pediatr. 1975 Jan-Feb;8(1):68-71.
4
5
Autosomal syndromes.常染色体综合征
Pediatr Ann. 1978 Jun;7(6):94-5, 97-100, 102-7 passim.
6
[Translocation t(2q-; 21q+) in three generations].三代人中的[2号染色体长臂缺失；21号染色体长臂增加易位]
Ann Genet. 1968 Mar;11(1):28-32.
7
[Familial translocation t(6; 18) (q16; q16; q23) with free 21 trisomy].[伴有游离21三体的家族性6号与18号染色体易位t(6; 18) (q16; q16; q23)]
Ann Genet. 1974 Dec;17(4):275-7.
8
The importance of chromosome analysis in Down's syndrome. A case report of a 21-21 translocation.
Ohio State Med J. 1966 Jan;62(1):40-3.
9
Probable reciprocal translocation in somatic cells from patients with Down's syndrome.唐氏综合征患者体细胞中可能存在的相互易位。
Jinrui Idengaku Zasshi. 1974 Sep;19(2):169-73.
10
Down's syndrome associated with a familial (21q-; 22q+) translocation.
Cytogenetics. 1967;6(5):321-30.
引用本文的文献
1
Familial balanced translocation 4p+/17q- as a suggested cause of primary trisomy-21 Down's syndrome.家族性4号染色体短臂增加/17号染色体长臂缺失平衡易位作为原发性21三体唐氏综合征的一个可能病因。
Arch Dis Child. 1977 Nov;52(11):890-3. doi: 10.1136/adc.52.11.890.
Zotero 插件