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Genomic and clinical characteristics of six patients with partially overlapping interstitial deletions at 10p12p11.
Wentzel C, Rajcan-Separovic E, Ruivenkamp CA, Chantot-Bastaraud S, Metay C, Andrieux J, Annerén G, Gijsbers AC, Druart L, Hyon C, Portnoi MF, Stattin EL, Vincent-Delorme C, Kant SG, Steinraths M, Marlin S, Giurgea I, Thuresson AC. Wentzel C, et al. Eur J Hum Genet. 2011 Sep;19(9):959-64. doi: 10.1038/ejhg.2011.71. Epub 2011 Apr 27. Eur J Hum Genet. 2011. PMID: 21522184 Free PMC article.
Clinical variability of the 22q11.2 duplication syndrome.
Wentzel C, Fernström M, Ohrner Y, Annerén G, Thuresson AC. Wentzel C, et al. Eur J Med Genet. 2008 Nov-Dec;51(6):501-10. doi: 10.1016/j.ejmg.2008.07.005. Epub 2008 Jul 29. Eur J Med Genet. 2008. PMID: 18707033
Mutations in HECW2 are associated with intellectual disability and epilepsy.
Halvardson J, Zhao JJ, Zaghlool A, Wentzel C, Georgii-Hemming P, Månsson E, Ederth Sävmarker H, Brandberg G, Soussi Zander C, Thuresson AC, Feuk L. Halvardson J, et al. Among authors: wentzel c. J Med Genet. 2016 Oct;53(10):697-704. doi: 10.1136/jmedgenet-2016-103814. Epub 2016 Jun 22. J Med Genet. 2016. PMID: 27334371 Free PMC article.
Pathogenesis of diabetes-induced congenital malformations.
Eriksson UJ, Borg LA, Cederberg J, Nordstrand H, Simán CM, Wentzel C, Wentzel P. Eriksson UJ, et al. Among authors: wentzel p, wentzel c. Ups J Med Sci. 2000;105(2):53-84. doi: 10.1517/03009734000000055. Ups J Med Sci. 2000. PMID: 11095105 Review.
Autism screening: an unsupervised machine learning approach.
Thabtah F, Spencer R, Abdelhamid N, Kamalov F, Wentzel C, Ye Y, Dayara T. Thabtah F, et al. Among authors: wentzel c. Health Inf Sci Syst. 2022 Sep 8;10(1):26. doi: 10.1007/s13755-022-00191-x. eCollection 2022 Dec. Health Inf Sci Syst. 2022. PMID: 36092454 Free PMC article.
40 results