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Biomedical Optics Express|August 28, 2019
Identification and investigation of the vibrational properties of crystalline and co-amorphous drugs with Raman and terahertz spectroscopyWei Liu, Yu Liu, Jiaoqi Huang, et al.
Orphanet Journal of Rare Diseases|November 15, 2011
Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicitiesCameron M Beech, Sandya Liyanarachchi, Nidhi P Shah, et al.
The American Journal of Physiology|January 14, 1999
Downregulated in adenoma gene encodes a chloride transporter defective in congenital chloride diarrheaR H Moseley, P Höglund, G D Wu, et al.
Investigative Ophthalmology & Visual Science|May 26, 2007
A novel CACNA1F gene mutation causes Aland Island eye diseaseReetta Jalkanen, N Torben Bech-Hansen, Rose Tobias, et al.
Bioconjugate Chemistry|September 15, 2018
Lactose-Modified Chitosan Gold(III)-PEGylated Complex-Bioconjugates: From Synthesis to Interaction with Targeted Galectin-1 ProteinQiqian Liu, Pasquale Sacco, Eleonora Marsich, et al.
The Journal of Clinical Endocrinology and Metabolism|July 27, 2016
Genome-Wide Expression Screening Discloses Long Noncoding RNAs Involved in Thyroid CarcinogenesisSandya Liyanarachchi, Wei Li, Pearlly Yan, et al.
Clinical Genetics|April 16, 2003
Identification of a deletion in the mismatch repair gene, MSH2, using mouse-human cell hybrids monosomal for chromosome 2R E Pyatt, H Nakagawa, H Hampel, et al.
American Journal of Human Genetics|October 1, 1988
Linkage relationships and gene order around the locus for X-linked retinoschisisT Alitalo, H Forsius, J Kärnä, et al.
Nature Genetics|December 1, 1994
Loss of the wild type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancerA Hemminki, P Peltomäki, J P Mecklin, et al.
Journal of Medical Genetics|August 19, 2008
A novel mutation in the sulfate transporter gene SLC26A2 (DTDST) specific to the Finnish population causes de la Chapelle dysplasiaL Bonafé, J Hästbacka, A de la Chapelle, et al.
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