Long arm deletion of the X chromosome, 46,X,del(xX)(q21), associated with gonadoblastoma.
作者信息
Seki T, Fujimoto S, Abe S, Sasaki M, Kawaguchi I, Kikukawa H, Kikuchi Y, Ichinoe K
出版信息
Jinrui Idengaku Zasshi. 1981 Dec;26(4):307-12. doi: 10.1007/BF01876362.
PMID:7345190
Abstract
摘要
相似文献
1
Long arm deletion of the X chromosome, 46,X,del(xX)(q21), associated with gonadoblastoma.X染色体长臂缺失，46,X,del(xX)(q21)，与性腺母细胞瘤相关。
Jinrui Idengaku Zasshi. 1981 Dec;26(4):307-12. doi: 10.1007/BF01876362.
2
[Dysgerminoma and gonadoblastoma in a phenotypic female with 45, X/47, XYY mosaicism].
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[Chromosome X with partial long arm deletion. Three cases].[X染色体长臂部分缺失。三例]
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[Bone malformations associated with deletion of the long arm of chromosome X].与X染色体长臂缺失相关的骨骼畸形
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7
[Chromosomal anomalies in men with infertility].[不育男性的染色体异常]
Urol Nefrol (Mosk). 1991 Sep-Oct(5):53-5.
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46,XX/46,XX,8p- mosaicism in a phenotypically normal female.一名表型正常女性存在46,XX/46,XX,8p-嵌合体。
Ann Genet. 1985;28(2):123-4.
9
Gonadoblastoma in a patient with an isodicentric X chromosome.
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10
Deletion of the long arm of chromosome 11 and sex chromosome constitution.11号染色体长臂缺失与性染色体组成
Am J Med Genet. 1985 Feb;20(2):401-2. doi: 10.1002/ajmg.1320200223.
引用本文的文献
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Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features.特纳综合征与女性性染色体畸变：推导临床特征发展中涉及的主要因素。
Hum Genet. 1995 Jun;95(6):607-29. doi: 10.1007/BF00209476.
2
The similarity of phenotypic effects caused by Xp and Xq deletions in the human female: a hypothesis.人类女性中Xp和Xq缺失所导致的表型效应的相似性：一种假说。
Hum Genet. 1990 Jul;85(2):175-83. doi: 10.1007/BF00193192.
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