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Scoliosis in association with the 22q11.2 deletion syndrome: an observational study.
Homans JF, Baldew VGM, Brink RC, Kruyt MC, Schlösser TPC, Houben ML, Deeney VFX, Crowley TB, Castelein RM, McDonald-McGinn DM. Homans JF, et al. Among authors: deeney vfx. Arch Dis Child. 2019 Jan;104(1):19-24. doi: 10.1136/archdischild-2018-314779. Epub 2018 Apr 7. Arch Dis Child. 2019. PMID: 29627765
What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia.
Campbell IM, Sheppard SE, Crowley TB, McGinn DE, Bailey A, McGinn MJ, Unolt M, Homans JF, Chen EY, Salmons HI, Gaynor JW, Goldmuntz E, Jackson OA, Katz LE, Mascarenhas MR, Deeney VFX, Castelein RM, Zur KB, Elden L, Kallish S, Kolon TF, Hopkins SE, Chadehumbe MA, Lambert MP, Forbes BJ, Moldenhauer JS, Schindewolf EM, Solot CB, Moss EM, Gur RE, Sullivan KE, Emanuel BS, Zackai EH, McDonald-McGinn DM. Campbell IM, et al. Among authors: deeney vfx. Am J Med Genet A. 2018 Oct;176(10):2058-2069. doi: 10.1002/ajmg.a.40637. Am J Med Genet A. 2018. PMID: 30380191 Free PMC article.
The 22q11.2 deletion syndrome as a model for idiopathic scoliosis - A hypothesis.
Homans JF, de Reuver S, Breetvelt EJ, Vorstman JAS, Deeney VFX, Flynn JM, McDonald-McGinn DM, Kruyt MC, Castelein RM. Homans JF, et al. Among authors: deeney vfx. Med Hypotheses. 2019 Jun;127:57-62. doi: 10.1016/j.mehy.2019.03.024. Epub 2019 Mar 27. Med Hypotheses. 2019. PMID: 31088649 Free article.
22q11.2 Deletion Syndrome as a Human Model for Idiopathic Scoliosis.
de Reuver S, Homans JF, Schlösser TPC, Houben ML, Deeney VFX, Crowley TB, Stücker R, Pasha S, Kruyt MC, McDonald-McGinn DM, Castelein RM. de Reuver S, et al. Among authors: deeney vfx. J Clin Med. 2021 Oct 20;10(21):4823. doi: 10.3390/jcm10214823. J Clin Med. 2021. PMID: 34768342 Free PMC article.
30 results