A case of true hermaphroditism reveals an unusual mechanism of twinning-Reference-Cited by-同舟云学术

A case of true hermaphroditism reveals an unusual mechanism of twinning

Published:2006-12-13 Issue:2 Volume:121 Page:179-185
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Souter Vivienne L.,Parisi Melissa A.,Nyholt Dale R.,Kapur Raj P.,Henders Anjali K.,Opheim Kent E.,Gunther Daniel F.,Mitchell Michael E.,Glass Ian A.,Montgomery Grant W.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-006-0279-x.pdf

Reference16 articles.

1. Benirschke K (1970) Spontaneous chimerism in mammals A critical review. Curr Top Pathol 51:1–61

2. Boklage CE (1987) The organization of the oocyte and embryogenesis in twinning and fusion malformations. Acta Genet Med Gemellol 36:421–431

3. Dewald G, Haymond MW, Spurbeck JL, Moore SB (1980) Origins of chi46,XX/46,XY chimerism in a human true hermaphrodite. Science 207:321–323

4. Giltay JC, Brunt T, Beemer FA, Wit JM, Ploos van Amstel HK, Pearson PL, Wijmenga C (1998) Polymorphc detection of a parthenogenetic maternal and double paternal contribution to a 46,XX/46,XY hermaphrodite. Am J Hum Genet 62:937–940

5. Golubovsky MD (2003) Postzygotic diploidization of triploids as a source of unusual cases of mosaicism, chimerism and twinning. Hum Reprod 18:236–242

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