Výsledky vyhledávání - "Wu, JerYuarn"

Periodical

Identification of a submicroscopic 3.2 Mb chromosomal 16q12.213 deletion in a child with short stature, mild developmental delay, and craniofacial anomalies, by highdensity oligonucleotide arraya recognizable syndromeHow to cite this article: Chang CF, Li LH, Wang CH, Tsai FJ, Chen TC, Wu JY, Chen YT, Tsai A.C.H. 2010. Identification of a submicroscopic 3.2 Mb chromosomal 16q12.213 deletion in a child with short stature, mild developmental delay, and craniofacial anomalies, by highdensity oligonucleotide arraya recognizable syndrome. Am J Med Genet Part A 152A:2365–2371.

Autor: Chang, ChingFen, Li, LingHui, Wang, ChungHsing, Tsai, FuuJen, Chen, TsaiChuan, Wu, JerYuarn, Chen, YuanTsong, Tsai, Anne ChunHui

Publikováno v: American Journal of Medical Genetics. Part A; September 2010, Vol. 152 Issue: 9 p2365-2371, 7p

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Periodical

A new familial insertion, ins18;9q12.2;q33.1q31.1 with a 9q31.1–9q33.1 deletion in a girl with a cleft lip and palateHow to Cite this Article: Chien SC, Li YC, Li LH, Wu JY, Hsu PC, Shi SL, Tsai FJ, Lin CC. 2010. A new familial insertion, ins18;9q12.2;q33.1q31.1 with a 9q31.1–9q33.1 deletion in a girl with a cleft lip and palate. Am J Med Genet Part A 152A:1862–1867.FuuJen Tsai and ChyiChyang Lin contributed equally to this work.

Autor: Chien, ShuChin, Li, YuehChun, Li, LingHui, Wu, JerYuarn, Hsu, PeiChing, Shi, SueLin, Tsai, FuuJen, Lin, ChyiChyang

Publikováno v: American Journal of Medical Genetics. Part A; July 2010, Vol. 152 Issue: 7 p1862-1867, 6p

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