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Items: 4

1.
Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1).
A Gehrig, U Felbor, R E Kelsell, D M Hunt, I H Maumenee, B H Weber
J Med Genet. 1998 Aug; 35(8): 641–645. doi: 10.1136/jmg.35.8.641
PMCID:
PMC1051388
SummaryPage BrowsePDF–1.0M
2.
Characterization of a Dominant Cone Degeneration in a Green Fluorescent Protein–Reporter Mouse with Disruption of Loci Associated with Human Dominant Retinal Dystrophy
Daniel M. Lipinski, Mohammed Yusuf, Alun R. Barnard, Christopher Damant, Peter Charbel Issa, Mandeep S. Singh, Edward Lee, Wayne L. Davies, Emanuela V. Volpi, Robert E. MacLaren
Invest Ophthalmol Vis Sci. 2011 Aug; 52(9): 6617–6623. Published online 2011 Aug 22. doi: 10.1167/iovs.11-7932
PMCID:
PMC3175985
AbstractArticlePDF–1.2M
3.
Exploring Implementation of Personal Breast Cancer Risk Assessments
Maria A. Sierra, Jack C. W. Wheeler, Lisa Devereux, Alison H. Trainer, Louise Keogh
J Pers Med. 2021 Oct; 11(10): 992. Published online 2021 Sep 30. doi: 10.3390/jpm11100992
PMCID:
PMC8541275
AbstractArticlePDF–260K
4.
Molecular analysis of the choroideremia gene related clinical findings in two families with choroideremia
Ying Lin, Xialin Liu, Lixia Luo, Bo Qu, Shuhong Jiang, Huiqin Yang, Xuanwei Liang, Shaobi Ye, Yizhi Liu
Mol Vis. 2011; 17: 2564–2569. Published online 2011 Sep 30.
PMCID:
PMC3198496
AbstractArticlePDF–737K

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