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。 - Suppr

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超能文献

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.

作者信息

Garson O M, Baikie A G, Ferguson J, Greer C H

出版信息

J Med Genet. 1969 Jun;6(2):209-15. doi: 10.1136/jmg.6.2.209.

DOI:10.1136/jmg.6.2.209

PMID:5801469

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1468840/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5563/1468840/15872a363efe/jmedgene00373-0100-a.jpg

相似文献

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。

J Med Genet. 1969 Jun;6(2):209-15. doi: 10.1136/jmg.6.2.209.

Trisomy D-trisomy E mosaicism in an infant male.一名男婴的D三体-E三体嵌合体

J Med Genet. 1971 Sep;8(3):384-6. doi: 10.1136/jmg.8.3.384.

Double autosomal trisomy (trisomy D+G) with mosaicism.伴有嵌合体的双常染色体三体（D+G三体）

J Med Genet. 1969 Sep;6(3):347-8. doi: 10.1136/jmg.6.3.347.

[Mosaicism between normal diploid and 18-trisomic cell population (46, XX/47, XXE18+) with weak expression of 18-trisomic cell line].[正常二倍体与18-三体细胞群体（46,XX/47,XX,+18）之间的嵌合体，18-三体细胞系表达较弱]

Monatsschr Kinderheilkd (1902). 1976 May;124(5):462-4.

A double aneuploid mosaic: trisomy 13 and XXY.双非整倍体嵌合体：13三体和克氏综合征（XXY）

J Med Genet. 1972 Sep;9(3):365-7. doi: 10.1136/jmg.9.3.365.

Frequency of chromosomal aberrations in newborn infants with multiple developmental defects.

Sov Genet. 1974 Sep 15;8(10):1329-30.

A case of mosaic trisomy 14 due to an isochromosome, i(14q).一例因等臂染色体i(14q)导致的14号染色体嵌合三体病例。

Jinrui Idengaku Zasshi. 1984 Mar;29(1):69-76. doi: 10.1007/BF01876761.

A live infant with trisomy 14 mosaicism and nuclear abnormalities of the neutrophils.一名患有14三体嵌合体和中性粒细胞核异常的活产婴儿。

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Trisomy 18 mosaicism in two siblings.

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Autosomal chromosome aberrations in ophthalmology.眼科中的常染色体畸变。

Int Ophthalmol Clin. 1968 Winter;8(4):839-910.

引用本文的文献

Trisomy D-trisomy E mosaicism in an infant male.一名男婴的D三体-E三体嵌合体

J Med Genet. 1971 Sep;8(3):384-6. doi: 10.1136/jmg.8.3.384.

Down's syndrome with 47,XX,+21-47,XX,+mar mosaicism.唐氏综合征，核型为47,XX,+21 - 47,XX,+mar嵌合体。

J Med Genet. 1973 Jun;10(2):177-9. doi: 10.1136/jmg.10.2.177.

Double aneuploidy (47,XX,21+-45,X) arising through simultaneous double non-disjunction.通过同时发生的双不分离产生的双非整倍体（47,XX,21±45,X）

J Med Genet. 1972 Jun;9(2):242-4. doi: 10.1136/jmg.9.2.242.

Double autosomal trisomy and mosaicism for chromosomes no. 8 and no. 21.

J Med Genet. 1974 Mar;11(1):96-101. doi: 10.1136/jmg.11.1.96.

Trisomy 21 with 47,+18 lymphocyte cell line: double mitotic nondisjunction.具有47，+18淋巴细胞系的21三体：双有丝分裂不分离。

J Med Genet. 1978 Oct;15(5):395-8. doi: 10.1136/jmg.15.5.395.

本文引用的文献

Mongoloid twins with 48 chromosomes (AA plus A21XXY).

Ann Hum Genet. 1961 Oct;25:111-5. doi: 10.1111/j.1469-1809.1961.tb01507.x.

Klinefelter's syndrome and mongolism in the same person.

Acta Paediatr (Stockh). 1960 Jul;49:536-9. doi: 10.1111/j.1651-2227.1960.tb07769.x.

A CASE OF DOUBLE AUTOSOMAL TRISOMY WITH MOSAICISM: 48/XX (TRISOMY 18+21) AND 46/XX.一例伴有嵌合体的双常染色体三体综合征：48/XX（18号染色体三体+21号染色体三体）和46/XX。

J Pediatr. 1965 Jun;66:1055-60. doi: 10.1016/s0022-3476(65)80092-0.

THE ANOMALOUS EMBRYONIC DEVELOPMENT ASSOCIATED WITH TRISOMY 13-15.与13 - 15三体相关的异常胚胎发育。

Am J Clin Pathol. 1965 Apr;43:334-47. doi: 10.1093/ajcp/43.4.334.

MULTIPLE CHROMOSOMAL ABNORMALITIES IN AN ACUTE EXACERBATION OF MYELOID LEUKAEMIA.急性髓系白血病急性加重期的多种染色体异常

Lancet. 1965 Mar 13;1(7385):609-10. doi: 10.1016/s0140-6736(65)91202-x.

TRISOMY 17-18(E): STUDIES IN LONG-TERM SURVIVAL WITH REPORT OF TWO AUTOPSIED CASES.

Pediatrics. 1964 Oct;34:533-41.

THE PATHOLOGY OF 18 TRISOMY.

J Pediatr. 1964 Jul;65:92-101. doi: 10.1016/s0022-3476(64)80557-6.

PATHOGENESIS OF POLYCYSTIC KIDNEYS. TYPE 3 DUE TO MULTIPLE ABNORMALITIES OF DEVELOPMENT.多囊肾的发病机制。3型源于多种发育异常。

Arch Pathol. 1964 May;77:485-502.

DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME.染色体三体中的发育性血红蛋白异常：D1三体综合征

Proc Natl Acad Sci U S A. 1964 Jan;51(1):89-97. doi: 10.1073/pnas.51.1.89.

NUCLEAR ABNORMALITIES OF THE NEUTROPHILS IN D1 (13-15)-TRISOMY SYNDROME.13-15 号染色体三体综合征中性粒细胞的核异常

Lancet. 1964 Mar 14;1(7333):589-90. doi: 10.1016/s0140-6736(64)91336-4.

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