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Automatic recognition of the XLHED phenotype from facial images.
Hadj-Rabia S, Schneider H, Navarro E, Klein O, Kirby N, Huttner K, Wolf L, Orin M, Wohlfart S, Bodemer C, Grange DK. Hadj-Rabia S, et al. Am J Med Genet A. 2017 Sep;173(9):2408-2414. doi: 10.1002/ajmg.a.38343. Epub 2017 Jul 10. Am J Med Genet A. 2017. PMID: 28691769
Craniofacial morphometric analysis of individuals with X-linked hypohidrotic ectodermal dysplasia.
Goodwin AF, Larson JR, Jones KB, Liberton DK, Landan M, Wang Z, Boekelheide A, Langham M, Mushegyan V, Oberoi S, Brao R, Wen T, Johnson R, Huttner K, Grange DK, Spritz RA, Hallgrímsson B, Jheon AH, Klein OD. Goodwin AF, et al. Among authors: klein od. Mol Genet Genomic Med. 2014 Sep;2(5):422-9. doi: 10.1002/mgg3.84. Epub 2014 May 20. Mol Genet Genomic Med. 2014. PMID: 25333067 Free PMC article.
Characterization of X-linked hypohidrotic ectodermal dysplasia (XL-HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging.
Jones KB, Goodwin AF, Landan M, Seidel K, Tran DK, Hogue J, Chavez M, Fete M, Yu W, Hussein T, Johnson R, Huttner K, Jheon AH, Klein OD. Jones KB, et al. Among authors: klein od. Am J Med Genet A. 2013 Jul;161A(7):1585-93. doi: 10.1002/ajmg.a.35959. Epub 2013 May 17. Am J Med Genet A. 2013. PMID: 23687000 Free PMC article.
Body size and allometric variation in facial shape in children.
Larson JR, Manyama MF, Cole JB, Gonzalez PN, Percival CJ, Liberton DK, Ferrara TM, Riccardi SL, Kimwaga EA, Mathayo J, Spitzmacher JA, Rolian C, Jamniczky HA, Weinberg SM, Roseman CC, Klein O, Lukowiak K, Spritz RA, Hallgrimsson B. Larson JR, et al. Am J Phys Anthropol. 2018 Feb;165(2):327-342. doi: 10.1002/ajpa.23356. Epub 2017 Nov 27. Am J Phys Anthropol. 2018. PMID: 29178597 Free PMC article.
Genomewide Association Study of African Children Identifies Association of SCHIP1 and PDE8A with Facial Size and Shape.
Cole JB, Manyama M, Kimwaga E, Mathayo J, Larson JR, Liberton DK, Lukowiak K, Ferrara TM, Riccardi SL, Li M, Mio W, Prochazkova M, Williams T, Li H, Jones KL, Klein OD, Santorico SA, Hallgrimsson B, Spritz RA. Cole JB, et al. Among authors: klein od. PLoS Genet. 2016 Aug 25;12(8):e1006174. doi: 10.1371/journal.pgen.1006174. eCollection 2016 Aug. PLoS Genet. 2016. PMID: 27560698 Free PMC article.
Dental findings in 14q terminal deletion syndrome.
Mendelsohn BA, Jeng LLB, Oberoi S, Klein OD. Mendelsohn BA, et al. Among authors: klein od. Clin Dysmorphol. 2014 Apr;23(2):60-62. doi: 10.1097/MCD.0000000000000026. Clin Dysmorphol. 2014. PMID: 24535103 No abstract available.
245 results