患者存在（6；15）易位并伴有染色体物质缺失，家庭成员存在各种染色体畸变。 - Suppr

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超能文献

(6;15) Translocation with loss of chromosome material in the patient and various chromosome aberrations in family members.

作者信息

Mikkelsen M, Dyggve H

出版信息

Humangenetik. 1973 May 25;18(3):195-202. doi: 10.1007/BF00290596.

DOI:10.1007/BF00290596

PMID:4124199

Abstract

摘要

相似文献

(6;15) Translocation with loss of chromosome material in the patient and various chromosome aberrations in family members.患者存在（6；15）易位并伴有染色体物质缺失，家庭成员存在各种染色体畸变。

Humangenetik. 1973 May 25;18(3):195-202. doi: 10.1007/BF00290596.

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Origin of the marker chromosomes in an established hypotriploid glioma cell line studies with G-band technique.

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引用本文的文献

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Translocation between chromosomes 6 and 15 (45,XX,t(6;15)(q25;q11.2)) with further evidence for lack of imprinting of the insulin-like growth factor II/mannose-6-phosphate receptor in humans.6号和15号染色体之间的易位（45,XX,t(6;15)(q25;q11.2)），并有进一步证据表明人类胰岛素样生长因子II/甘露糖-6-磷酸受体缺乏印记。

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Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.15号染色体异常与普拉德-威利综合征：细胞遗传学分析

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Unbalanced reciprocal translocations in cases of Prader-Willi syndrome.普拉德-威利综合征病例中的不平衡相互易位

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Karyotype 45,XX,-21/46,XX,21q-in an infant with symptoms of G-deletion syndrome I.核型为45，XX，-21/46，XX，21q-的一名患有I型G缺失综合征症状的婴儿。

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De novo (11;13) translocation.

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本文引用的文献

[PARTIAL DELETION OF THE SHORT ARM OF CHROMOSOME 5. INDIVIDUALIZATION OF A NEW MORBID STATE].

Sem Hop. 1964 Apr 14;40:1069-79.

[Deficiency on the short arms of a chromosome No. 4].[4号染色体短臂缺失]

Humangenetik. 1965;1(5):397-413.

Differential binding of alkylating fluorochromes in human chromosomes.烷化荧光染料在人类染色体中的差异结合

Exp Cell Res. 1970 Jun;60(3):315-9. doi: 10.1016/0014-4827(70)90523-9.

The 13q-deletion syndrome.13q缺失综合征

Am J Hum Genet. 1969 Sep;21(5):499-512.

The 4p- syndrome. A clinically recognizable chromosomal deletion syndrome.4p-综合征。一种临床上可识别的染色体缺失综合征。

Am J Dis Child. 1971 Nov;122(5):421-5.

Localization of heterochromatin in human chromosomes.人类染色体中异染色质的定位

Cytogenetics. 1971;10(2):81-6. doi: 10.1159/000130130.

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