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Current Opinion in Ophthalmology|July 28, 2015
The current status of molecular diagnosis of inherited retinal dystrophiesJohn Pei-wen Chiang, Karmen TrzupekAmerican Journal of Medical Genetics. Part A|November 26, 2009
Evidence suggesting digenic inheritance of Waardenburg syndrome type II with ocular albinismPei-Wen Chiang, Elaine Spector, Tracy L McGregorAmerican Journal of Medical Genetics. Part A|March 23, 2012
Café-au-lait macules and intertriginous freckling in piebaldism: clinical overlap with neurofibromatosis type 1 and Legius syndromeCathy A Stevens, Pei-Wen Chiang, Ludwine M MessiaenCurrent Opinion in Genetics & Development|June 6, 2003
Human and mouse disorders of pigmentationRichard A Spritz, Pei Wen Chiang, Naoki Oiso, et al.Genes|January 27, 2021
The Novel Halovirus Hardycor1, and the Presence of Active (Induced) Proviruses in Four HaloarchaeaMike Dyall-Smith, Friedhelm Pfeiffer, Pei-Wen Chiang, et al.Genome Announcements|February 14, 2018
Draft Genome Sequence of <i>Endozoicomonas acroporae</i> Strain Acr-14<sup>T</sup>, Isolated from <i>Acropora</i> CoralKshitij Tandon, Pei-Wen Chiang, Wen-Ming Chen, et al.Microbiology Resource Announcements|May 14, 2021
Genome Sequence of Hardyhisp2, a Gammapleolipovirus Infecting Haloarcula hispanicaMike Dyall-Smith, Friedhelm Pfeiffer, Pei-Wen Chiang, et al.JAMA Ophthalmology|March 20, 2015
Autosomal Dominant Retinal Dystrophy With Electronegative Waveform Associated With a Novel RAX2 MutationPaul Yang, Pei-Wen Chiang, Richard G Weleber, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|August 29, 2020
Molecular and phenotypic investigation of a New Zealand cohort of childhood-onset retinal dystrophySarah Hull, Gulunay Kiray, John Pei-Wen Chiang, et al.Pageof 7