[Trisomy 22: a new clinical entity? Clinical and cytogenetic study of a case].
作者信息
Buffoni L, Vianello M G, Reboa E, Tarateta A, Bonioli E
出版信息
Minerva Pediatr. 1974 Dec 1;26(38):1895-901.
PMID:4453319
Abstract
摘要
相似文献
1
[Trisomy 22: a new clinical entity? Clinical and cytogenetic study of a case].[22三体综合征：一种新的临床实体？1例病例的临床与细胞遗传学研究]
Minerva Pediatr. 1974 Dec 1;26(38):1895-901.
2
[2 cases of trisomy 11q(q23.2-- qter) with the same abnormality of external genitalia].2例11号染色体长臂（q23.2-qter）三体伴相同外生殖器异常
Ann Genet. 1975 Sep;18(3):179-84.
3
[Smith-Lemli-Opitz syndrome. Case report and differential diagnosis].[史密斯-莱姆利-奥皮茨综合征。病例报告及鉴别诊断]
Minerva Pediatr. 1982 Sep 15;34(17):709-14.
4
[Partial trisomy of chromosome 22 in an infant].[一名婴儿的22号染色体部分三体性]
Pediatr Pol. 1983 Jun;58(6):561-4.
5
Congenital heart diseases and chromosomal abnormalities. A scientific exhibit.
Nebr Med J. 1972 Apr;57(4):119-20.
6
[Clinical aspects of chromosomal aberrations - problems of semiotics and nosography].[染色体畸变的临床方面——符号学与疾病分类学问题]
Padiatr Padol Suppl. 1975;4:32-47.
7
Trisomy of the short arm of chromosome number 9: a clinical entity.9号染色体短臂三体：一种临床实体。
Acta Paediatr Belg. 1980;Suppl 13:97-104.
8
Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p.一名患有多种先天性异常的活产婴儿中的非嵌合性9号染色体短臂四体：病例报告及与9号染色体短臂三体的比较
Am J Med Genet. 1996 Jun 14;63(3):434-7. doi: 10.1002/(SICI)1096-8628(19960614)63:3<434::AID-AJMG4>3.0.CO;2-R.
9
[A case of the Moebius syndrome with symptoms similar to the 18 p- syndrome, but with normal karyotype].
Neurol Psihiatr Neurochir. 1974 Jan-Feb;19(1):27-32.
10
[A chemical and karyological study in a case of dyscraniotic oligophrenia].
Folia Hered Pathol (Milano). 1968 Jul;17(3):103-12.
引用本文的文献
1
Trisomy 22 with 'cat eye' anomaly.伴有“猫眼”异常的22三体综合征。
J Med Genet. 1977 Aug;14(4):288-90. doi: 10.1136/jmg.14.4.288.
Zotero 插件