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Page 1
3q26.33-3q27.2 microdeletion: a new microdeletion syndrome?
Eur J Med Genet. 2013 Apr;56(4):216-21. doi: 10.1016/j.ejmg.2013.01.005. Epub 2013 Jan 26.
Eur J Med Genet. 2013.
PMID: 23357683
Free article.
Mosaic structural variation in children with developmental disorders.
King DA, Jones WD, Crow YJ, Dominiczak AF, Foster NA, Gaunt TR, Harris J, Hellens SW, Homfray T, Innes J, Jones EA, Joss S, Kulkarni A, Mansour S, Morris AD, Parker MJ, Porteous DJ, Shihab HA, Smith BH, Tatton-Brown K, Tolmie JL, Trzaskowski M, Vasudevan PC, Wakeling E, Wright M, Plomin R, Timpson NJ, Hurles ME; Deciphering Developmental Disorders Study.
King DA, et al. Among authors: hellens sw.
Hum Mol Genet. 2015 May 15;24(10):2733-45. doi: 10.1093/hmg/ddv033. Epub 2015 Jan 29.
Hum Mol Genet. 2015.
PMID: 25634561
Free PMC article.
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Microdeletion 1p35.2: a recognizable facial phenotype with developmental delay.
Wilson BT, Omer M, Hellens SW, Zwolinski SA, Yates LM, Lynch SA.
Wilson BT, et al. Among authors: hellens sw.
Am J Med Genet A. 2015 Aug;167A(8):1916-20. doi: 10.1002/ajmg.a.37114. Epub 2015 Apr 21.
Am J Med Genet A. 2015.
PMID: 25900906
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Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease.
Soemedi R, Wilson IJ, Bentham J, Darlay R, Töpf A, Zelenika D, Cosgrove C, Setchfield K, Thornborough C, Granados-Riveron J, Blue GM, Breckpot J, Hellens S, Zwolinkski S, Glen E, Mamasoula C, Rahman TJ, Hall D, Rauch A, Devriendt K, Gewillig M, O' Sullivan J, Winlaw DS, Bu'Lock F, Brook JD, Bhattacharya S, Lathrop M, Santibanez-Koref M, Cordell HJ, Goodship JA, Keavney BD.
Soemedi R, et al. Among authors: hellens s.
Am J Hum Genet. 2012 Sep 7;91(3):489-501. doi: 10.1016/j.ajhg.2012.08.003. Epub 2012 Aug 30.
Am J Hum Genet. 2012.
PMID: 22939634
Free PMC article.
Item in Clipboard
Mitral valve replacement for the treatment of congenital mitral dysplasia in a bull terrier.
White RN, Stepien RL, Hammond RA, Holden DJ, Torrington AM, Milner HR, Cobb MA, Hellens SH.
White RN, et al. Among authors: hellens sh.
J Small Anim Pract. 1995 Sep;36(9):407-10. doi: 10.1111/j.1748-5827.1995.tb02968.x.
J Small Anim Pract. 1995.
PMID: 8583770
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A case of mosaic trisomy 19q12-q13.2 with high BMI, macrocephaly, and speech delay: does USF2 determine size in the 19q phenotypes?
Wilson BT, Newby R, Watts K, Hellens SW, Zwolinski SA, Splitt MP.
Wilson BT, et al. Among authors: hellens sw.
Clin Dysmorphol. 2012 Jan;21(1):33-36. doi: 10.1097/MCD.0b013e32834e7f9f.
Clin Dysmorphol. 2012.
PMID: 22107929
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Interstitial microduplication 12q13.2-q13.3 in a patient with dysmorphism, developmental delay, atypical seizures and hypospadias: not a phenocopy of Wolf-Hirschhorn syndrome.
Wilson BT, Hellens SW, Breese GJ, Zwolinski SA, Wright MJ.
Wilson BT, et al. Among authors: hellens sw.
Clin Dysmorphol. 2012 Oct;21(4):196-199. doi: 10.1097/MCD.0b013e328356d409.
Clin Dysmorphol. 2012.
PMID: 22772582
No abstract available.
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