Molecular analysis of a 4p deletion associated with Wolf-Hirschhorn syndrome and congenital glaucoma.

被引:0
|
作者
Finzi, S
Franchi-Pinto, C
Cohen, R
Hida, RY
Wiggs, JL
机构
[1] NEMC, Ophthalmol, Boston, MA USA
[2] NEMC, Div Genet, Boston, MA USA
[3] Fac Ciencias Med Santa Casa, Sao Paulo, Brazil
[4] Irmandade Santa Casa Misericordia, Sao Paulo, Brazil
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D O I
暂无
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
4367B314
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页码:S823 / S823
页数:1
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