Skip to main content

. 1970 Mar;7(1):1–4. doi: 10.1136/jmg.7.1.1

Xq- Turner's syndrome: reconsideration of hypothesis that Xp- causes somatic features in Turner's syndrome.

F Hecht, D L Jones, M Delay, H Klevit

PMCID: PMC1468913 PMID: 5480961

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

BECKER K. L., PARIS J., ALBERT A. OVARIAN DYSGENESIS DUE TO DELETION OF THE X CHROMOSOME. Proc Staff Meet Mayo Clin. 1963 Aug 28;38:389–394. [PubMed] [Google Scholar]
Bender M. A., Kastenbaum M. A. Statistical analysis of the normal human karyotype. Am J Hum Genet. 1969 Jul;21(4):322–351. [PMC free article] [PubMed] [Google Scholar]
FERGUSON-SMITH M. A. KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS. J Med Genet. 1965 Jun;2(2):142–155. doi: 10.1136/jmg.2.2.142. [DOI] [PMC free article] [PubMed] [Google Scholar]
JACOBS P. A., HARNDEN D. G., BUCKTON K. E., BROWN W. M., KING M. J., McBRIDE J. A., MACGREGOR T. N., MACLEAN N. Cytogenetic studies in primary amenorrhoea. Lancet. 1961 Jun 3;1(7188):1183–1189. doi: 10.1016/s0140-6736(61)91939-0. [DOI] [PubMed] [Google Scholar]
Jacobs P. A. Structural abnormalities of the sex chromosomes. Br Med Bull. 1969 Jan;25(1):94–98. doi: 10.1093/oxfordjournals.bmb.a070676. [DOI] [PubMed] [Google Scholar]
Lejeune J., Doumic J. M., Berger R., Rethoré M. O. Sur un cas de dysgénésie ovarienne XXdc. Ann Genet. 1966 Sep;9(3):132–133. [PubMed] [Google Scholar]
PENROSE L. S. A NOTE ON THE MEAN MEASUREMENTS OF HUMAN CHROMOSOMES. Ann Hum Genet. 1964 Nov;28:195–196. doi: 10.1111/j.1469-1809.1964.tb00477.x. [DOI] [PubMed] [Google Scholar]
Steinberger E., Steinberger A., Smith K. D., Perloff W. H. Apparent deletion of X chromosome in a prepuberal girl. J Med Genet. 1966 Sep;3(3):226–229. doi: 10.1136/jmg.3.3.226. [DOI] [PMC free article] [PubMed] [Google Scholar]

ACTIONS

RESOURCES