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38篇 您的检索式：作者名="Heon E"

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	题名	作者	年代	出处	被引量
1	Further genetic heterogeneity for autosomal dominant human sutural cataracts显示文摘	Klopp N Heon E Billingsley G	2003	Ophthalmic Res2003，35，：	1
2	Analysis of myocilin mutations in 1703 glaucoma patients from five different popula- tions显示文摘	Fingert JH Heon E Liebmann JM	1999	Hum Mol Genet1999，8，：	1
3	N:w locus for autosomal dominanthigh myopia maps to the long arm of chromosome 17显示文摘	Paluru P Ronan SM Heon E	2003	Invest Ophthalmol Vis Sci2003，44，5：	1
4	TRIPS, pharmaceutical patens, and access to essential medicines: a long way from Seattle to Doha 显示文摘	Heon E	2002	Chicago Journal of International Law2002，，3：	1
5	Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25显示文摘	Mirzayans F Gould DB Heon E	2000	Eur J Hum Genet2000，8，：	1
6	New locus for auto- soma显示文摘	PALURU P RONAN SM HEON E eta	2003	Invest Ophthalmol Vis Sci2003，44，5：	1
7	The gamma-crystallins and human cataracts:a puzzle made clearer显示文摘	Heon E Priston M Schorederet D	1999	Am J Hum Genet1999，65，：	1
8	Jpn JAppl Phys Part l显示文摘	Kim J S Kang J Y Heon P E	2004	43(3): 9892004，43，3：	1
9	The gamma-crystallins and human cataracts:a puzzle made clearer显示文摘	Heon E Priston M Schorderet DF	1999	Am J Hum Genet1999，65，：	1
10	Analysis of myocilin mutations in 1703 glaucoma patients from five different populations显示文摘	Fingert JH Heon E Liebmann JM	1999	Hum Mol genet1999，8，：	1
11	Domain disruption and mutation of the bZIP transcription factor,MAF,associated with cataract,ocular anterior segment dysgenesis and coloboma显示文摘	Jamieson RV Perveen R Kerr B Carette M Yardley J Heon E	2002	Hum Mol Genet2002，11，：	1
12	High-resolution retinal imaging in young children using a handheld scanner and Fourier- domain optical coherence tomography 显示文摘	Gerth C Zawadzki RJ Heon E	2009	J AAPOS2009，13，1：	1
13	The ganuna-crystallins and human cataracts: a puzzle made clearer显示文摘	Heon E Priston M Schorderet DF Billingsley GD Girard PO Lubsen N	1999	Am J Hum Genet1999，65，5：	1
14	Ocular phenotypes of three genetic variants of Bardet-Biedl syndrome显示文摘	Heon E Westall C Carmi R	2005	Am J Med Genet A2005，132，3：	1
15	Analysis of myocilin mutations in I 703 glaucoma patients from five different populations 显示文摘	Fingert JH Heon E Liebmann JM	1999	Hum Mol Genet1999，8，5：	1
16	The gamma-crystallins and human cataracts : a puzzle made clearer 显示文摘	Heon E Priston M Hnm E	1999	Am J Genet1999，65，：	1
17	New locus for autosomal dominant high myopia maps to the long arm of chromosome 17显示文摘	Paluru P Ronan SM Heon E	2003	Invest Ophthalmol Vis Sci2003，44，5：	1
18	New locus for autosomal dominant high myopia maps to the long arm of chromosome 17显示文摘	Paluru P Ronan SM Heon E Devoto M Wildenberg SC Scavello G	2003	Invest Ophthalmol Vis Sci2003，44，5：	1
19	Vsx1:a Gene for Posterior Polymorphous Dystrophy and Keratoconus显示文摘	HEON E GREENBERG A KOPP K K	2002	Hum Mol Genet2002，11，：	1
20	New locus for autosomal dominant high myopia maps to the long arm of chromosome 17 显示文摘	Paluru P Ronan SM Heon E	2003	Invest Ophthalmol Vis Sci2003，44，5：	1

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