C8 trisomy mosaicism syndrome.
作者信息
Bijlsma J B, Wijffels J C, Tegelaers W H
出版信息
Helv Paediatr Acta. 1972 Jul;27(3):281-98.
PMID:4645654
Abstract
摘要
相似文献
1
C8 trisomy mosaicism syndrome.8号染色体三体嵌合综合征
Helv Paediatr Acta. 1972 Jul;27(3):281-98.
2
[Autosomal chromosome aberrations].[常染色体畸变]
Bord Med. 1971 May;4(5):1373-416.
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4
5
Partial trisomy 9 in the case of familial translocation 8/9 mat.家族性8号/9号染色体母系易位情况下的9号染色体部分三体
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Partial trisomy of chromosome 11: a case report.11号染色体部分三体：一例报告
Am J Ment Defic. 1973 Jan;77(4):383-8.
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[Cp trisomy: a new syndrome].[18号染色体三体：一种新综合征]
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8
[The intelligence level in the chromosome aberrations affecting autosomes].[影响常染色体的染色体畸变中的智力水平]
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["Free" 9p trisomy in a male child with severe mental retardation (author's transl)].一名患有严重智力迟钝男童的“游离型”9号染色体三体（作者译）
An Esp Pediatr. 1979 May;12(5):463-8.
10
46,XY-47,XY,C+ mosaicism in a male infant with multiple anomalies.一名患有多种异常的男婴存在46,XY - 47,XY,C+嵌合体现象。
Ann Genet. 1969 Jun;12(2):102-6.
引用本文的文献
1
Trisomy 8. Report of a mosaic human male with near-normal phenotype and normal IQ, ascertained through infertility.8号染色体三体。通过不孕症确诊的一名表型接近正常且智商正常的嵌合型男性患者的报告。
Hum Genet. 1980;55(1):31-8. doi: 10.1007/BF00329123.
2
Trisomy-8 syndrome.8三体综合征
Humangenetik. 1974 Jun 26;23(1):23-9. doi: 10.1007/BF00295679.
3
Brother and sister with trisomy 10p: a new syndrome.患有10号染色体短臂三体综合征的兄妹：一种新综合征。
Humangenetik. 1974;23(3):163-72. doi: 10.1007/BF00285102.
4
A familial translocation t(6q+;8q-) identified by fluorescence microscopy.通过荧光显微镜鉴定出的家族性易位t(6q+;8q-)
Humangenetik. 1973 Apr 16;18(2):189-92. doi: 10.1007/BF00291490.
5
The tirsomy 8 syndrome: two additional mosaic cases.8三体综合征：另外两例嵌合型病例
J Med Genet. 1974 Dec;11(4):393-8. doi: 10.1136/jmg.11.4.393.
6
Dermatoglyphics in trisomy 8 mosaicism.8号染色体三体嵌合体的皮纹学
Humangenetik. 1974;24(3):201-5. doi: 10.1007/BF00283585.
7
Partial trisomy 8 (8q24) and the trisomy-8 syndrome.8号染色体部分三体（8q24）与8号染色体三体综合征
Humangenetik. 1974;23(4):297-303. doi: 10.1007/BF00272513.
8
Partial trisomy 8: trisomy of the distal part of the long arm of chromosome number 8 plus (8q2) in a severely retarded and malformed girl.8号染色体部分三体：一名重度智力发育迟缓且畸形的女孩出现8号染色体长臂远端（8q2）三体。
Humangenetik. 1974;24(3):241-6. doi: 10.1007/BF00283593.
9
Familial trisomy 7 mosaicism.家族性7号染色体三体嵌合体
J Med Genet. 1975 Jun;12(2):200-3. doi: 10.1136/jmg.12.2.200.
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Trisomy 8 mosaicism. A case report and a proposed list of the clinical features.
Eur J Pediatr. 1976 Nov 3;123(4):293-300. doi: 10.1007/BF00444650.
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