青春期前女孩X染色体的明显缺失。 - Suppr

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超能文献

Apparent deletion of X chromosome in a prepuberal girl.

作者信息

Steinberger E, Steinberger A, Smith K D, Perloff W H

出版信息

J Med Genet. 1966 Sep;3(3):226-9. doi: 10.1136/jmg.3.3.226.

DOI:10.1136/jmg.3.3.226

PMID:5971058

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1012944/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7d1/1012944/24c43c8bf6f1/jmedgene00328-0070-a.jpg

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引用本文的文献

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本文引用的文献

Asynchronous duplication of human chromosomes and the origin of sex chromatin.人类染色体的异步复制与性染色质的起源

Proc Natl Acad Sci U S A. 1962 May 15;48(5):756-63. doi: 10.1073/pnas.48.5.756.

TURNER'S SYNDROME WITH SECONDARY AMENORRHOEA AND SEX CHROMOSOME MOSAICISM.特纳综合征伴继发性闭经和性染色体镶嵌现象

Acta Endocrinol (Copenh). 1964 Jul;46:341-51. doi: 10.1530/acta.0.0460341.

Time-sequence of human chromosome duplication.人类染色体复制的时间序列。

Nature. 1962 Sep 1;195:869-73. doi: 10.1038/195869a0.

Procedure for routine clinical determination of urinary gonadotropin.尿促性腺激素常规临床测定方法

Proc Staff Meet Mayo Clin. 1955 Nov 16;30(23):552-6.

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