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。 - Suppr

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On the localization of genes on certain autosomes of man through chromosome aberrations. 3. Exclusion of the possibility of gene assignment.

作者信息

Bender K, Burckhardt K

出版信息

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

DOI:10.1007/BF00696016

PMID:5488998

Abstract

摘要

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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。

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引用本文的文献

Localization exclusion of the HL-A genes from the short arm of human chromosome 5.

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本文引用的文献

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Am J Hum Genet. 1965 Sep;17(5):410-9.

MEIOTIC AND MITOTIC STUDIES OF A FAMILIAL RECIPROCAL TRANSLOCATION BETWEEN TWO AUTOSOMES OF GROUP 6-12.6-12组两条常染色体间家族性相互易位的减数分裂和有丝分裂研究

Cytogenetics. 1965;4:45-64. doi: 10.1159/000129843.

PARTIAL DELETION OF THE SHORT ARMS OF A CHROMOSOME OF THE 4-5 GROUP (DENVER).第4-5组（丹佛）染色体短臂的部分缺失

Arch Dis Child. 1965 Feb;40(209):82-5. doi: 10.1136/adc.40.209.82.

"CRI DU CHAT" SYNDROME. A NEW CLINICAL AND CYTOGENETIC ENTITY.“猫叫综合征”。一种新的临床和细胞遗传学实体。

Lancet. 1965 Jan 2;1(7375):23-5. doi: 10.1016/s0140-6736(65)90926-8.

[17-18 RING-CHROMOSOMES AND CONGENITAL MALFORMATIONS IN A YOUNG GIRL].[一名年轻女孩的17 - 18号环状染色体与先天性畸形]

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[THE CRYING CAT SYNDROME: A FURTHER CASE].[哭泣猫综合征：又一例病例]

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DELETION OF THE SHORT ARM OF CHROMOSOME 18.18号染色体短臂缺失

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PARTIAL DELETION OF SHORT ARMS OF CHROMOSOME NO. 5. REPORT OF A CASE IN A FRATERNAL TWIN.

Am J Dis Child. 1965 Jan;109:85-9. doi: 10.1001/archpedi.1965.02090020087011.

THE "CAT CRY" SYNDROME.“猫叫”综合征

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