Abdelmalik N - Search Results

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Diagnostic outcomes of 27 children referred by pediatricians to a genetics clinic in the Netherlands with suspicion of fetal alcohol spectrum disorders.

Abdelmalik N, van Haelst M, Mancini G, Schrander-Stumpel C, Marcus-Soekarman D, Hennekam R, Cobben JM. Abdelmalik N, et al. Am J Med Genet A. 2013 Feb;161A(2):254-60. doi: 10.1002/ajmg.a.35672. Epub 2013 Jan 9. Am J Med Genet A. 2013. PMID: 23303648

A fetus with de novo 2q33.2q35 deletion including MAP2 with brain anomalies, esophageal atresia, and laryngeal stenosis.

van Binsbergen E, Ellis RJ, Abdelmalik N, Jarvis J, Randhawa K, Wyatt-Ashmead J, Canham N, Thorpe-Beeston JG, Mancini GM, Van Haelst MM. van Binsbergen E, et al. Among authors: abdelmalik n. Am J Med Genet A. 2014 Jan;164A(1):194-8. doi: 10.1002/ajmg.a.36202. Epub 2013 Nov 15. Am J Med Genet A. 2014. PMID: 24243657

Effect of the selective serotonin reuptake inhibitor paroxetine on platelet function is modified by a SLC6A4 serotonin transporter polymorphism.

Abdelmalik N, Ruhé HG, Barwari K, van den Dool EJ, Meijers JC, Middeldorp S, Büller HR, Schene AH, Kamphuisen PW. Abdelmalik N, et al. J Thromb Haemost. 2008 Dec;6(12):2168-74. doi: 10.1111/j.1538-7836.2008.03196.x. Epub 2008 Oct 18. J Thromb Haemost. 2008. PMID: 18983505 Free article. Clinical Trial.

[A girl with a lacunar skull].

Abdelmalik N, Op de Coul ME. Abdelmalik N, et al. Ned Tijdschr Geneeskd. 2010;154:A1595. Ned Tijdschr Geneeskd. 2010. PMID: 21176262 Dutch.

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