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American Journal of Medical Genetics. Part A|October 18, 2023
A case of mosaic deletion of paternally-inherited PLAGL1 and two cases of upd(6)mat add to evidence for PLAGL1 under-expression as a cause of growth restrictionAhmed S N Alhendi, Gabriella Gazdagh, Derek Lim, et al.
Clinical Epigenetics|July 2, 2014
Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjectsAbdulla Ibrahim, Gail Kirby, Carol Hardy, et al.
Journal of Medical Genetics|June 17, 2021
Whole-genome analysis as a diagnostic tool for patients referred for diagnosis of Silver-Russell syndrome: a real-world studyAhmed S N Alhendi, Derek Lim, Shane McKee, et al.
Plos Genetics|March 21, 2009
Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome)Esther Meyer, Derek Lim, Shanaz Pasha, et al.
Photodermatology, Photoimmunology & Photomedicine|September 26, 2023
Photopatch testing in Singapore: A 10-year retrospective studyShi Yu Derek Lim, Anthony Teik-Jin Goon, Yung Hian Leow, et al.
JID Innovations : Skin Science From Molecules to Population Health|July 21, 2022
Expression of <i>Staphylococcus aureus</i> Virulence Factors in Atopic DermatitisSi En Poh, Winston L C Koh, Shi Yu Derek Lim, et al.
Human Reproduction (Oxford, England)|December 17, 2008
Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologiesDerek Lim, Sarah C Bowdin, Louise Tee, et al.
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