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Genome-wide sequencing and the clinical diagnosis of genetic disease: The CAUSES study.
Elliott AM, Adam S, du Souich C, Lehman A, Nelson TN, van Karnebeek C, Alderman E, Armstrong L, Aubertin G, Blood K, Boelman C, Boerkoel C, Bretherick K, Brown L, Chijiwa C, Clarke L, Couse M, Creighton S, Watts-Dickens A, Gibson WT, Gill H, Tarailo-Graovac M, Hamilton S, Heran H, Horvath G, Huang L, Hulait GK, Koehn D, Lee HK, Lewis S, Lopez E, Louie K, Niederhoffer K, Matthews A, Meagher K, Peng JJ, Patel MS, Race S, Richmond P, Rupps R, Salvarinova R, Seath K, Selby K, Steinraths M, Stockler S, Tang K, Tyson C, van Allen M, Wasserman W, Mwenifumbo J, Friedman JM. Elliott AM, et al. Among authors: steinraths m. HGG Adv. 2022 Apr 18;3(3):100108. doi: 10.1016/j.xhgg.2022.100108. eCollection 2022 Jul 14. HGG Adv. 2022. PMID: 35599849 Free PMC article.
CCMG guidelines: prenatal and postnatal diagnostic testing for uniparental disomy.
Dawson AJ, Chernos J, McGowan-Jordan J, Lavoie J, Shetty S, Steinraths M, Wang JC, Xu J; Canadian College of Medical Geneticists committees. Dawson AJ, et al. Among authors: steinraths m. Clin Genet. 2011 Feb;79(2):118-24. doi: 10.1111/j.1399-0004.2010.01547.x. Epub 2010 Oct 12. Clin Genet. 2011. PMID: 21039433
Recurrent sterile abscesses in a case of X-linked neutropenia.
Biggs CM, Modi B, Steinraths M, Del Bel K, Pourshahnazari P, Griffiths C, Forrest DM, Prendiville J, Dutz JP, Turvey SE, Cameron SB. Biggs CM, et al. Among authors: steinraths m. Pediatr Dermatol. 2020 Jul;37(4):742-744. doi: 10.1111/pde.14146. Epub 2020 Mar 23. Pediatr Dermatol. 2020. PMID: 32202653
Bone health and SATB2-associated syndrome.
Zarate YA, Steinraths M, Matthews A, Smith WE, Sun A, Wilson LC, Brain C, Allgove J, Jacobs B, Fish JL, Powell CM, Wasserman WW, van Karnebeek CD, Wakeling EL, Ma NS. Zarate YA, et al. Among authors: steinraths m. Clin Genet. 2018 Mar;93(3):588-594. doi: 10.1111/cge.13121. Epub 2017 Dec 27. Clin Genet. 2018. PMID: 28787087 Review.
21 results