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Localization of the ICF syndrome to chromosome 20 by homozygosity mapping.
Wijmenga C, van den Heuvel LP, Strengman E, Luyten JA, van der Burgt IJ, de Groot R, Smeets DF, Draaisma JM, van Dongen JJ, De Abreu RA, Pearson PL, Sandkuijl LA, Weemaes CM. Wijmenga C, et al. Among authors: de abreu ra, de groot r. Am J Hum Genet. 1998 Sep;63(3):803-9. doi: 10.1086/302021. Am J Hum Genet. 1998. PMID: 9718351 Free PMC article.
Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome).
Hagleitner MM, Lankester A, Maraschio P, Hultén M, Fryns JP, Schuetz C, Gimelli G, Davies EG, Gennery A, Belohradsky BH, de Groot R, Gerritsen EJ, Mattina T, Howard PJ, Fasth A, Reisli I, Furthner D, Slatter MA, Cant AJ, Cazzola G, van Dijken PJ, van Deuren M, de Greef JC, van der Maarel SM, Weemaes CM. Hagleitner MM, et al. Among authors: de greef jc, de groot r. J Med Genet. 2008 Feb;45(2):93-9. doi: 10.1136/jmg.2007.053397. Epub 2007 Sep 24. J Med Genet. 2008. PMID: 17893117
Reviewing Omenn syndrome.
Aleman K, Noordzij JG, de Groot R, van Dongen JJ, Hartwig NG. Aleman K, et al. Among authors: de groot r. Eur J Pediatr. 2001 Dec;160(12):718-25. doi: 10.1007/s004310100816. Eur J Pediatr. 2001. PMID: 11795679 Review.
Analysing the developing lymphocyte system of neonates and infants.
de Vries E, de Groot R, de Bruin-Versteeg S, Comans-Bitter WM, van Dongen JJ. de Vries E, et al. Among authors: de bruin versteeg s, de groot r. Eur J Pediatr. 1999 Aug;158(8):611-7. doi: 10.1007/s004310051162. Eur J Pediatr. 1999. PMID: 10445337 Review.
835 results