信函：人类半乳糖-1-磷酸尿苷酰转移酶基因的定位 - Suppr

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Letter: Localisation of human gene for galactose-1-phosphate-uridyltransferase.

作者信息

Allerdice P W, Tedesco T A

出版信息

Lancet. 1975 Jul 5;2(7923):39. doi: 10.1016/s0140-6736(75)92988-8.

DOI:10.1016/s0140-6736(75)92988-8

PMID:49636

Abstract

摘要

相似文献

Letter: Localisation of human gene for galactose-1-phosphate-uridyltransferase.信函：人类半乳糖-1-磷酸尿苷酰转移酶基因的定位

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[Determination of reference ranges for the activity of galactose-1-phosphate uridyltransferase (E.C. 2.7.7.12) in the blood using a simple optimized method of determination and comparison with the results of a half-quantitative screening method].

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[Galactosemia; variability in clinical aspects and problems in the diagnosis].[半乳糖血症；临床症状的变异性及诊断中的问题]

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[The electrophoretic stability of galactose-1-phosphate-uridyltransferase (E.C.2.7.7.12) after aging under various methods of preservation].[不同保存方法老化后1-磷酸半乳糖尿苷酰转移酶（E.C.2.7.7.12）的电泳稳定性]

Beitr Gerichtl Med. 1980;38:263-6.

引用本文的文献

Where is the gene for GALT?半乳糖-1-磷酸尿苷酰转移酶基因位于哪里？

Hum Genet. 1980;54(1):129-30. doi: 10.1007/BF00279064.

Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21).3号染色体q21重复导致qter缺失，p25导致pter综合征，见于臂间倒位inv(3)(p25q21)携带者的子女。

Am J Hum Genet. 1975 Nov;27(6):699-718.

A case of trisomy 3q21 leads to qter syndrome.

Hum Genet. 1979 Jan 25;46(2):141-7. doi: 10.1007/BF00291914.

Localisation of the human ABO: Np-1: AK-1 linkage group by regional assignment of AK-1 to 9q34.人类ABO血型定位：通过将AK-1基因定位到9q34区域，确定其与Np-1:AK-1连锁群的关系。

Hum Genet. 1976 Sep 10;34(1):35-43. doi: 10.1007/BF00284432.

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