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Cultured epithelial autografts: three years of clinical experience with eighteen patients. [electronic resource] by
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Calcification inhibitors and Wnt signaling proteins are implicated in bovine artery smooth muscle cell calcification in the presence of phosphate and vitamin D sterols. [electronic resource] by
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Mutation of a new gene causes a unique form of Hermansky-Pudlak syndrome in a genetic isolate of central Puerto Rico. [electronic resource] by
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Aspirated bile: a major host trigger modulating respiratory pathogen colonisation in cystic fibrosis patients. [electronic resource] by
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Acute humoral rejection in renal allograft recipients: I. Incidence, serology and clinical characteristics. [electronic resource] by
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Transplantation vol. 71
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A Phase II Toxicity End Point Trial (ICORG 99-09) of Accelerated Dose-escalated Hypofractionated Radiation in Non-small Cell Lung Cancer. [electronic resource] by
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Assessment of American College of Rheumatology quality criteria for rheumatoid arthritis in a pre-quality criteria patient cohort. [electronic resource] by
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Partial NSD1 deletions cause 5% of Sotos syndrome and are readily identifiable by multiplex ligation dependent probe amplification. [electronic resource] by
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HPP1: a transmembrane protein-encoding gene commonly methylated in colorectal polyps and cancers. [electronic resource] by
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Application of explicit process of care measurement to rheumatoid arthritis: Moving from evidence to practice. [electronic resource] by
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FISH mapping of de novo apparently balanced chromosome rearrangements identifies characteristics associated with phenotypic abnormality. [electronic resource] by
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- Harewood, L
- Holloway, S
- Sharkey, F
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- van Heyningen, V
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Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting. [electronic resource] by
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- Mendoza-Londono, R
- den Hollander, N S
- Ruivenkamp, C
- Maher, E
- Tanke, H J
- Szuhai, K
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A critical role for Dnmt1 and DNA methylation in T cell development, function, and survival. [electronic resource] by
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- Schlissel, M S
- Nguyen, S
- Cherry, S R
- Tsai, J H
- Tucker, S M
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Clinical and mutation data in 12 patients with the clinical diagnosis of Nager syndrome. [electronic resource] by
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- Hoogeboom, A J
- Kayserili, H
- Simsek-Kiper, P O
- Klein-Hitpass, L
- Kuechler, A
- López-González, V
- Martin, M
- Rahmann, S
- Schweiger, B
- Splitt, M
- Wollnik, B
- Lüdecke, H-J
- Zeschnigk, M
- Wieczorek, D
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In:
Human genetics vol. 132
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