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Familial occurrence of trisomy 22.

作者信息

Uchida I A, Ray M, McRae K N, Besant D F

出版信息

Am J Hum Genet. 1968 Mar;20(2):107-18.

PMID:5643178
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1706268/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d43/1706268/c2d92a9b38d2/ajhg00386-0027-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d43/1706268/5cb8eb80b2dd/ajhg00386-0021-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d43/1706268/95248515fe96/ajhg00386-0023-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d43/1706268/71a48d4f88c4/ajhg00386-0024-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d43/1706268/d479d8c870e3/ajhg00386-0025-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d43/1706268/c2d92a9b38d2/ajhg00386-0027-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d43/1706268/5cb8eb80b2dd/ajhg00386-0021-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d43/1706268/95248515fe96/ajhg00386-0023-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d43/1706268/71a48d4f88c4/ajhg00386-0024-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d43/1706268/d479d8c870e3/ajhg00386-0025-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d43/1706268/c2d92a9b38d2/ajhg00386-0027-a.jpg

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1
Familial occurrence of trisomy 22.22三体综合征的家族性发生情况。
Am J Hum Genet. 1968 Mar;20(2):107-18.
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引用本文的文献

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2
Incomplete trisomy 22. I. Familial 11/22 translocation with 3:1 meiotic disjunction. Delineation of a common clinical picture and report of nine new cases from six families.22号染色体三体不完整。I. 家族性11/22易位伴3:1减数分裂分离。常见临床症状的描述及来自六个家族的九例新病例报告。
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Aneuploidy of the chromosome G(21-22) autosomes. Current concepts.

本文引用的文献

1
[Apropos of a case of 22-trisomy].
Bull Acad R Med Belg. 1962;2:329-44.
2
CHROMOSOMES IN COLOBOMA AND ANAL ATRESIA.先天性虹膜缺损和肛门闭锁中的染色体
Lancet. 1965 Aug 7;2(7406):290. doi: 10.1016/s0140-6736(65)92415-3.
3
A PROBABLE CASE OF INCOMPLETE TRISOMY OF A CHROMOSOME OF THE 13-15 GROUP.一例可能的13 - 15组染色体不完全三体病例。
J Med Genet. 1965 Jun;2(2):136-41. doi: 10.1136/jmg.2.2.136.
染色体G组(21 - 22号)常染色体的非整倍性。当前概念
J Natl Med Assoc. 1971 Jul;63(4):238-40, 245.
4
Additional G-like chromosome in a malformed boy.一名畸形男孩体内额外的类G染色体。
J Med Genet. 1971 Jun;8(2):244-9. doi: 10.1136/jmg.8.2.244.
5
Short arm enlargement in acrocentric chromosomes.近端着丝粒染色体短臂增大。
Am J Hum Genet. 1969 May;21(3):293-304.
6
Morphology alone does not make an isochromosome.仅形态学特征不足以判定等臂染色体。
Hum Genet. 1986 Mar;72(3):253-5. doi: 10.1007/BF00291889.
7
Gene-rich chromosome regions and autosomal trisomy. A case of chromosome 3 trisomy mosaicism.基因丰富的染色体区域与常染色体三体性。一例3号染色体三体性嵌合体病例。
Hum Genet. 1987 Nov;77(3):214-20. doi: 10.1007/BF00284472.
8
Dermatoglyphic findings in 54 triple-X females and a review of some general principles applying to the soles in sex chromosome aneuploidy.54名XXX女性的皮纹学研究结果及性染色体非整倍体足底相关一般原则的综述
J Med Genet. 1975 Jun;12(2):185-92. doi: 10.1136/jmg.12.2.185.
9
Trisomy 22 mosaicism.22号染色体三体嵌合体
J Med Genet. 1977 Jun;14(3):224-5. doi: 10.1136/jmg.14.3.224.
10
47,XY,+der(11;22)(q23;q12) following balanced translocation t(11;22)(q23;q12)mat. Remarks on the problem of trisomy 22.47,XY,+der(11;22)(q23;q12),继发于母系平衡易位t(11;22)(q23;q12)。关于22三体问题的评论。
Hum Genet. 1977 Jun 10;37(1):111-6. doi: 10.1007/BF00293781.
4
IDENTIFICATION OF THE MONGOLISM CHROMOSOME BY DNA REPLICATION ANALYSIS.通过DNA复制分析鉴定唐氏综合征染色体
Am J Hum Genet. 1965 May;17(3):191-201.
5
DNA REPLICATION PATTERNS OF HUMAN CHROMOSOMES.人类染色体的DNA复制模式
Cytogenetics. 1963;2:175-93. doi: 10.1159/000129778.
6
ENLARGED SHORT ARM OR SATELLITE REGION-A HERITABLE TRAIT PROBABLY UNASSOCIATED WITH DEVELOPMENTAL DISORDER.
Cytogenetics. 1963;2:129-39. doi: 10.1159/000129774.
7
MANDIBULOFACIAL DYSOSTOSIS. REPORT OF TWO CASES WITH CHROMOSOME ANALYSIS.
Am J Dis Child. 1964 Mar;107:304-7.
8
A familial chromosome abnormality associated with repeated abortions.
Cytogenetics. 1962;1:199-209. doi: 10.1159/000129729.
9
Another child with 47 chromosomes.
Med J Aust. 1963 Apr 13;50(1):546-7.
10
An apparently identical extra autosome in two severely retarded sisters with multiple malformations.
Cytogenetics. 1962;1:32-41. doi: 10.1159/000129711.