Frequency and occurrence of chromosomal syndromes. I. D-Trisomy.
作者信息
Conen P E, Erkman B
出版信息
Am J Hum Genet. 1966 Jul;18(4):374-86.
Abstract
摘要
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Frequency and occurrence of chromosomal syndromes: II. E-trisomy.染色体综合征的频率与发生率：II. E三体性
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Double autosomal trisomy and mosaicism for three cell lines in man: coexisting trisomy 13-15, trisomy 17-18, and a minority cell line trisomic for a chromosome of both groups.人类中双常染色体三体及三种细胞系的嵌合体：共存的13 - 15三体、17 - 18三体以及两组染色体三体的少数细胞系。
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本文引用的文献
1
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Am J Hum Genet. 1966 Jul;18(4):387-98.
2
Trisomy 13-15: a clinical syndrome.13 - 15三体综合征：一种临床综合征。
Lancet. 1961 Nov 4;2(7210):1001-2. doi: 10.1016/s0140-6736(61)90963-1.
3
Multiple congenital abnormalities associated with chromosomal trisomy.与染色体三体相关的多种先天性异常。
N Engl J Med. 1961 Aug 17;265:314-8. doi: 10.1056/NEJM196108172650703.
4
CHROMOSOME STUDIES IN SPONTANEOUS ABORTIONS.自然流产的染色体研究
Obstet Gynecol. 1965 Sep;26:308-26.
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SPORADIC TRISOMY D1 WITH TRANSLOCATION D-D.伴有D-D易位的散发性1号染色体三体
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AUTOSOMAL ABNORMALITIES.常染色体异常。
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ANATOMIC AND HISTOPATHOLOGIC STUDY OF TWO CASES OF D1 (13-15) TRISOMY.两例13 - 15号染色体三体（D1）的解剖学与组织病理学研究
Cytogenetics. 1964;3:258-84.
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AUTOSOMAL TRISOMY SYNDROMES, EXCLUDING DOWN'S.常染色体三体综合征，不包括唐氏综合征。
Guys Hosp Rep. 1964;113:231-49.
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DEOXYRIBONUCLEIC-ACID REPLICATION PATTERN OF TRISOMY D1.三体 D1 的脱氧核糖核酸复制模式
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FOETAL HAEMOGLOBIN AND NEUTROPHIL ANOMALY IN THE D1-TRISOMY SYNDROME.13号染色体三体综合征中的胎儿血红蛋白与中性粒细胞异常
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