Found: 11
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A Novel IVS2-1G>A Mutation Causes Aberrant Splicing of the HRPT2 Gene in a Family with Hyperparathyroidism-Jaw Tumor Syndrome.
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- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 2, p. 878, doi. 10.1210/jc.2004-0991
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- Article
Identification of a novel U2 HR mutation in a Korean woman with Marie Unna hereditary hypotrichosis.
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- International Journal of Dermatology, 2014, v. 53, n. 11, p. 1358, doi. 10.1111/ijd.12545
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- Article
Triangulated Irregular Network based Seamline Determination for Fast Image Stitching of Multiple UAV Images.
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- International Archives of the Photogrammetry, Remote Sensing & Spatial Information Sciences, 2024, v. 48, n. 2, p. 449, doi. 10.5194/isprs-archives-XLVIII-2-2024-449-2024
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- Article
Seamline Optimization Based on Triangulated Irregular Network of Tiepoints for Fast UAV Image Mosaicking.
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- Remote Sensing, 2024, v. 16, n. 10, p. 1738, doi. 10.3390/rs16101738
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- Article
Fast UAV Image Mosaicking by a Triangulated Irregular Network of Bucketed Tiepoints.
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- Remote Sensing, 2023, v. 15, n. 24, p. 5782, doi. 10.3390/rs15245782
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- Article
A high-resolution map of human chromosome 12.
- Published in:
- Nature, 2001, v. 409, n. 6822, p. 945, doi. 10.1038/35057174
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- Article
What Can We Obtain from Mental Health Care? The Dynamics of Physical and Mental Health.
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- International Journal of Environmental Research & Public Health, 2019, v. 16, n. 17, p. 3098, doi. 10.3390/ijerph16173098
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- Article
Translocation breakpoints upstream of the HMGIC gene in uterine leiomyomata suggest dysregulation of this gene by a mechanism different from that in lipomas.
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- Genes, Chromosomes & Cancer, 1996, v. 17, n. 1, p. 1, doi. 10.1002/(SICI)1098-2264(199609)17:1<1::AID-GCC1>3.0.CO;2-0
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- Article
Ischemic Colitis after Iliac Stenting.
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- Korean Journal of Vascular & Endovascular Surgery, 2013, v. 29, n. 1, p. 23, doi. 10.5758/kjves.2013.29.1.23
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- Article
Preoperative Endovascular Abdominal Aortic Aneurysm Repair Planning with Centerline Measurement.
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- Korean Journal of Vascular & Endovascular Surgery, 2013, v. 29, n. 1, p. 6, doi. 10.5758/kjves.2013.29.1.6
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- Article
Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene.
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- Human Molecular Genetics, 2001, v. 10, n. 3, p. 283, doi. 10.1093/hmg/10.3.283
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- Article