Association of the X chromosomal region q11→22 and Klinefelter syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1981.tb00721.x/fullpdf
Reference13 articles.
1. Spreading of inactivation in an (X;14) translocation;Allderdice;Amer. J. med. Genet.,1978
2. Chromatin in Klinefelter's syndrome;Bradbury;J. clin. endocrinol. Metab.,1956
3. A 47, XXq-Y Klinefelter male;Chandra;J. med. Genet.,1971
4. Unusual chromosomal variant in Klinefelter syndrome;Gardiner;Brit. med. J.,1978
5. A case of human intersexuality having a possible XXY sex-determining mechanism;Jacobs;Nature,1959
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1. A rare variant Klinefelter syndrome seen 40 years later: 47,X,del(Xq24),Y;Andrologia;2021-08-10
2. Chromosomal Aberrations in Turkish Infertile Couples with Reproductive Problems;Global Journal of Fertility and Research;2016-07-18
3. Chromosomal Variants in Klinefelter Syndrome;Sexual Development;2011
4. Klinefelter syndrome and the Xq1l-22 region;Clinical Genetics;2008-04-23
5. Variant Klinefelter syndrome 47,X,i(X)(q10),Y and normal 46,XY karyotype in monozygotic adult twins;American Journal of Medical Genetics Part A;2007
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