[决定12号染色体短臂三体性的家族性Cc-F易位] - Suppr

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[Familial Cc-F translocation determining a trisomy for the short arm of chromosome 12].

作者信息

Lejeuen J, Berger R, Réthoré M O, Salmon C, Kaplan M

出版信息

Ann Genet. 1966;9(1):12-8.

PMID:5295698

Abstract

摘要

相似文献

[Familial Cc-F translocation determining a trisomy for the short arm of chromosome 12].[决定12号染色体短臂三体性的家族性Cc-F易位]

Ann Genet. 1966;9(1):12-8.

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[Trisomy 10p as a result of familial 10/22 translocation].[由于家族性10/22易位导致的10号染色体短臂三体]

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[Familial observation of partial trisomy 6, and probable partial monosomy 18q by parental translocation].[6号染色体部分三体及可能的18q部分单体的家族性观察，源于父母染色体易位]

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引用本文的文献

Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation.推定9号染色体短臂三体性，非遗传性易位所致。

Humangenetik. 1971;12(3):175-81. doi: 10.1007/BF00702772.

On the localization of genes on certain autosomes of man through chromosome aberrations. 3. Exclusion of the possibility of gene assignment.通过染色体畸变对人类某些常染色体上基因的定位。3. 排除基因定位的可能性。

Humangenetik. 1970;9(1):75-85. doi: 10.1007/BF00696016.

Identification of a familial 19-21 translocation by Q and G band patterns.通过Q带和G带模式鉴定家族性19 - 21易位

Humangenetik. 1973 May 25;18(3):219-24. doi: 10.1007/BF00290600.

Trisomy 12p due to familial t(12p-,6q plus) translocation.因家族性t(12p-,6q+)易位导致的12号染色体短臂三体

Humangenetik. 1974;24(3):247-52.

[Giemsa-R-banding analysis of the trisomy 9p and report of a new case].9号染色体短臂三体的吉姆萨R显带分析及1例新病例报告

Humangenetik. 1973 Apr 16;18(2):129-38. doi: 10.1007/BF00291480.

47,+(9q-) in unrelated three children with plasma growth hormone deficiency.47，+（9q-）见于三名无亲缘关系的患有血浆生长激素缺乏症的儿童。

Hum Genet. 1976 Mar 12;31(3):271-82. doi: 10.1007/BF00270857.

Trisomy 9p resulting from maternal 9/21 translocation.由母亲的9号与21号染色体易位导致的9号染色体短臂三体。

Hum Genet. 1976 May 19;32(2):217-20. doi: 10.1007/BF00291508.

Genetics of the +p9 syndrome.+p9综合征的遗传学

Hum Genet. 1976 Apr 15;32(1):23-33. doi: 10.1007/BF00569973.

Trisomy 9p resulting from de novo 9/15 translocation and a 9p isochromosome.由新发9/15易位和9号染色体短臂等臂染色体导致的9号染色体短臂三体。

Hum Genet. 1979 Nov;52(2):175-8. doi: 10.1007/BF00271570.

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