5q35 duplication and Hunter-McAlpine syndrome: missing the link.

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Ariana Kariminejad, Roxana Kariminejad, Andreas Tzschach, Reinhard Ullmann, Alisho Ahmed, Alaleh Asghari-Roodsari, Shadab Salehpour, Fariba Afroozan, Hans-Hilger Ropers, Mohammad Hasan Kariminejad, Craniosynostosis in a patient with 2q37.3 deletion 5q34 duplication: association of extra copy of MSX2 with craniosynostosis. American Journal of Medical Genetics Part A. ,vol. 149, pp. 1544- 1549 ,(2009) , 10.1002/AJMG.A.32949

Chih-Ping Chen, Shuan-Pei Lin, Chyi-Chyang Lin, Yann-Jang Chen, Schu-Rern Chern, Yueh-Chun Li, Lie-Jiau Hsieh, Chen-Chi Lee, Chen-Wen Pan, Wayseen Wang, Molecular cytogenetic analysis of de novo dup(5)(q35.2q35.3) and review of the literature of pure partial trisomy 5q. American Journal of Medical Genetics Part A. ,vol. 140, pp. 1594- 1600 ,(2006) , 10.1002/AJMG.A.31329

M ALANIS, B HURST, P MARSHBURN, M MATTHEWS, Conservative management of placenta increta with selective arterial embolization preserves future fertility and results in a favorable outcome in subsequent pregnancies Fertility and Sterility. ,vol. 86, pp. 1514- ,(2006) , 10.1016/J.FERTNSTERT.2006.02.128

David A. Koolen, Jos Herbergs, Joris A. Veltman, Rolph Pfundt, Hans van Bokhoven, Hans Stroink, Erik A. Sistermans, Han G. Brunner, Ad Geurts van Kessel, Bert B. A. de Vries, Holoprosencephaly and preaxial polydactyly associated with a 1.24 Mb duplication encompassing FBXW11 at 5q35.1 Journal of Human Genetics. ,vol. 51, pp. 721- 726 ,(2006) , 10.1007/S10038-006-0010-8

David Adam, Jonathan Knight, Journals under pressure: Publish, and be damned... Nature. ,vol. 419, pp. 772- 776 ,(2002) , 10.1038/419772A

Eda G. Utine, Yasemin Alanay, Dilek Aktas, Mehmet Alikasifoglu, Koray Boduroglu, Joris Vermeesch, Ergul Tuncbilek, Jean-Pierre Fryns, Cryptic trisomy 5q35.2qter and deletion 1p36.3 characterised using FISH and array-based CGH European Journal of Medical Genetics. ,vol. 51, pp. 343- 350 ,(2008) , 10.1016/J.EJMG.2008.03.002

C CHEN, C LIN, Y LI, L HSIEH, C LEE, W WANG, Primary ovarian failure in a mentally retarded woman with a de novo unbalanced X;autosome translocation Fertility and Sterility. ,vol. 86, ,(2006) , 10.1016/J.FERTNSTERT.2006.02.127