A double chromosomal aberration of the 47, XX, 21+-47, XXp-q-, 21+ type in a girl with features of Down's and Turner's syndromes. - Suppr | 超能文献

A double chromosomal aberration of the 47, XX, 21+-47, XXp-q-, 21+ type in a girl with features of Down's and Turner's syndromes.

作者信息

Mikel'saar A V, Blyumina M G, Kuznetsova L I, Mikel'saar R V, Lur'e I V

出版信息

Sov Genet. 1971 May;7(5):675-9.

Abstract

摘要

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Dual diagnoses in 152 patients with Turner syndrome: Knowledge of the second condition may lead to modification of treatment and/or surveillance.152 例特纳综合征患者的双重诊断：对第二状况的认识可能会导致治疗和/或监测的改变。

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2

Down's/Turner's mosaicism. Double aneuploidy as a rare cause of missed prenatal diagnosis of chromosomal abnormality.唐氏综合征/特纳综合征嵌合体。双非整倍体作为染色体异常产前漏诊的罕见原因。

Arch Dis Child. 1981 Dec;56(12):962-3. doi: 10.1136/adc.56.12.962.

3

Down and Turner syndromes in a female infant with 47,X,del(X)(p11),+21.一名患有47,X,del(X)(p11),+21的女婴的唐氏综合征和特纳综合征。

Hum Genet. 1977 Nov 2;39(1):103-8. doi: 10.1007/BF00273158.