Clinical consequence of Xp-
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00273321.pdf
Reference9 articles.
1. Bartsch-Sandhoff, M., Teninde, R., Wiegelmann, W., Scholz, W.: Karyotyp-Phenotyp-Korrelation bei einmen 46,X,del(X)(p22)-Befund. Hum. Genet. 31, 263?270 (1976)
2. Boczkowski, K., Mikkelsen, M.: Fluorescence and autoradiographic studies in patients with Turner's syndrome and 46,XXp-and 46,XXq-karyotypes. J. Med. Genet. 10, 350?355 (1973)
3. Bühler, E. M.: Evolution of X-chromosome inactivation. Lancet 1975 II, 1036
4. Fraccaro, M., Maraschio P., Pasquali, F., Scappaticci, S.: Women heterozygous for deficiency of the (p21-pter) region of the X chromosome are fertile. Hum. Genet. 39, 283?292 (1977)
5. Hecht, F., Jones, D. L., Delay, M., Klevit, H.: Xq-Turner's syndrome: Reconstruction of hypothesis that Xp-causes somatic features in Turner's syndrome. J. Med. Genet. 7, 1?4 (1970)
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1. Fertility in patients with X chromosome deletions;Clinical Genetics;2008-04-23
2. Structural anomalies of the X chromosome: personal observation and review of non-mosaic cases;Clinical Genetics;2008-04-23
3. Linear skin defects and congenital microphthalmia: a new syndrome at Xp22.2.;Journal of Medical Genetics;1991-02-01
4. The various phenotypes in Xp deletion. Observations in eleven patients;Human Genetics;1981-07
5. Segregation of an X ring chromosome in two generations.;Journal of Medical Genetics;1980-08-01
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