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Multiple abnormalities due to possible genetic inactivation in an X-autosome translocation.

作者信息

Thelen T H, Abrams D J, Fisch R O

出版信息

Am J Hum Genet. 1971 Jul;23(4):410-8.

Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f922/1706708/23a2b2e3997b/ajhg00370-0075-a.jpg

本文引用的文献

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RING CHROMOSOME MOSAICISM IN A SEVERELY SUBNORMAL CHILD WITH MULTIPLE CONGENITAL MALFORMATIONS.
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CYTOGENETIC AND CLINICAL FINDINGS IN 48 PATIENTS WITH CONGENITALLY DEFECTIVE OR ABSENT OVARIES.
Medicine (Baltimore). 1965 Mar;44:135-64. doi: 10.1097/00005792-196503000-00002.
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A MOUSE TRANSLOCATION SUPPRESSING SEX-LINKED VARIEGATION.
Cytogenetics. 1964;3:306-23. doi: 10.1159/000129820.
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ABSENCE OF LATE REPLICATION OF A HUMAN X-RING CHROMOSOME.
Nature. 1964 Nov 21;204:804-5. doi: 10.1038/204804b0.
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TURNER'S SYNDROME WITH SECONDARY AMENORRHOEA AND SEX CHROMOSOME MOSAICISM.
Acta Endocrinol (Copenh). 1964 Jul;46:341-51. doi: 10.1530/acta.0.0460341.
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H3-THYMIDINE UPTAKE BY A RING X CHROMOSOME IN A HUMAN FEMALE.
Proc Natl Acad Sci U S A. 1964 May;51(5):779-86. doi: 10.1073/pnas.51.5.779.
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Mammalian X-chromosome action: inactivation limited in spread and region of origin.
Science. 1963 May 31;140(3570):976-8. doi: 10.1126/science.140.3570.976.

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