Hoogeboom AJ - Search Results

1

Long-term functional outcome in 167 patients with syndromic craniosynostosis; defining a syndrome-specific risk profile.

de Jong T, Bannink N, Bredero-Boelhouwer HH, van Veelen ML, Bartels MC, Hoeve LJ, Hoogeboom AJ, Wolvius EB, Lequin MH, van der Meulen JJ, van Adrichem LN, Vaandrager JM, Ongkosuwito EM, Joosten KF, Mathijssen IM. de Jong T, et al. Among authors: hoogeboom aj. J Plast Reconstr Aesthet Surg. 2010 Oct;63(10):1635-41. doi: 10.1016/j.bjps.2009.10.029. Epub 2009 Nov 12. J Plast Reconstr Aesthet Surg. 2010. PMID: 19913472

2

[Genetics of craniofacial development].

van Adrichem LN, Hoogeboom AJ, Wolvius EB. van Adrichem LN, et al. Among authors: hoogeboom aj. Ned Tijdschr Tandheelkd. 2008 Feb;115(2):61-8. Ned Tijdschr Tandheelkd. 2008. PMID: 18326400 Review. Dutch.

3

Deletion of the TWIST gene in a large five-generation family.

De Heer IM, Hoogeboom AJ, Eussen HJ, Vaandrager JM, De Klein A. De Heer IM, et al. Among authors: hoogeboom aj. Clin Genet. 2004 May;65(5):396-9. doi: 10.1111/j.0009-9163.2004.00244.x. Clin Genet. 2004. PMID: 15099347

4

Phenotypes of craniofrontonasal syndrome in patients with a pathogenic mutation in EFNB1.

van den Elzen ME, Twigg SR, Goos JA, Hoogeboom AJ, van den Ouweland AM, Wilkie AO, Mathijssen IM. van den Elzen ME, et al. Among authors: hoogeboom aj. Eur J Hum Genet. 2014 Aug;22(8):995-1001. doi: 10.1038/ejhg.2013.273. Epub 2013 Nov 27. Eur J Hum Genet. 2014. PMID: 24281372 Free PMC article.

5

[From gene to disease; craniosynostosis syndromes due to FGFR2-mutation].

van Ravenswaaij-Arts CM, van den Ouweland AM, Hoogeboom AJ, Herbergs J, Pals G. van Ravenswaaij-Arts CM, et al. Among authors: hoogeboom aj. Ned Tijdschr Geneeskd. 2002 Jan 12;146(2):63-6. Ned Tijdschr Geneeskd. 2002. PMID: 11820058 Review. Dutch.

6

Deletion of 1 amino acid in Indian hedgehog leads to brachydactylyA1.

Lodder EM, Hoogeboom AJ, Coert JH, de Graaff E. Lodder EM, et al. Among authors: hoogeboom aj. Am J Med Genet A. 2008 Aug 15;146A(16):2152-4. doi: 10.1002/ajmg.a.32441. Am J Med Genet A. 2008. PMID: 18629882

7

Early diagnosis of Wolf-Hirschhorn syndrome triggered by a life-threatening event: congenital diaphragmatic hernia.

van Dooren MF, Brooks AS, Hoogeboom AJ, van den Hoonaard TL, de Klein JE, Wouters CH, Tibboel D. van Dooren MF, et al. Among authors: hoogeboom aj. Am J Med Genet A. 2004 Jun 1;127A(2):194-6. doi: 10.1002/ajmg.a.20613. Am J Med Genet A. 2004. PMID: 15108210

8

Clinical and mutation data in 12 patients with the clinical diagnosis of Nager syndrome.

Czeschik JC, Voigt C, Alanay Y, Albrecht B, Avci S, Fitzpatrick D, Goudie DR, Hehr U, Hoogeboom AJ, Kayserili H, Simsek-Kiper PO, Klein-Hitpass L, Kuechler A, López-González V, Martin M, Rahmann S, Schweiger B, Splitt M, Wollnik B, Lüdecke HJ, Zeschnigk M, Wieczorek D. Czeschik JC, et al. Among authors: hoogeboom aj. Hum Genet. 2013 Aug;132(8):885-98. doi: 10.1007/s00439-013-1295-2. Epub 2013 Apr 9. Hum Genet. 2013. PMID: 23568615

9

Undetected anomalies in foetuses with a prenatal diagnosis of isolated cleft.

Haj M, Koudstaal MJ, Ramcharan MS, Hoogeboom AJM, Koster MPH, Srebniak MI, Cohen-Overbeek TE. Haj M, et al. Among authors: hoogeboom ajm. Int J Oral Maxillofac Surg. 2020 Dec;49(12):1576-1583. doi: 10.1016/j.ijom.2020.05.005. Epub 2020 Jun 14. Int J Oral Maxillofac Surg. 2020. PMID: 32546322

10

First-trimester diagnosis of thrombocytopenia-absent radius syndrome using virtual reality.

Baken L, Groenenberg IAL, Hoogeboom AJM, Koning AHJ, Exalto N. Baken L, et al. Clin Dysmorphol. 2014 Apr;23(2):71-73. doi: 10.1097/MCD.0000000000000029. Clin Dysmorphol. 2014. PMID: 24556603 No abstract available.

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