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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1980 1
1983 3
1984 1
1985 2
1987 1
1991 1
1992 1
1998 1
2001 3
2002 2
2004 2
2006 1
2008 2
2009 4
2010 4
2011 3
2012 3
2013 6
2014 5
2015 7
2016 2
2017 7
2018 5
2020 1
2023 1
2024 1

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61 results

Results by year

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Page 1
Preaxial polydactyly of the foot.
Burger EB, Baas M, Hovius SER, Hoogeboom AJM, van Nieuwenhoven CA. Burger EB, et al. Among authors: hoogeboom ajm. Acta Orthop. 2018 Feb;89(1):113-118. doi: 10.1080/17453674.2017.1383097. Epub 2017 Sep 26. Acta Orthop. 2018. PMID: 28946786 Free PMC article. Review.
Disruption of TUFT1, a Desmosome-Associated Protein, Causes Skin Fragility, Woolly Hair, and Palmoplantar Keratoderma.
Verkerk AJMH, Andrei D, Vermeer MCSC, Kramer D, Schouten M, Arp P, Verlouw JAM, Pas HH, Meijer HJ, van der Molen M, Oberdorf-Maass S, Nijenhuis M, Romero-Herrera PH, Hoes MF, Bremer J, Slotman JA, van den Akker PC, Diercks GFH, Giepmans BNG, Stoop H, Saris JJ, van den Ouweland AMW, Willemsen R, Hublin JJ, Dean MC, Hoogeboom AJM, Silljé HHW, Uitterlinden AG, van der Meer P, Bolling MC. Verkerk AJMH, et al. Among authors: hoogeboom ajm. J Invest Dermatol. 2024 Feb;144(2):284-295.e16. doi: 10.1016/j.jid.2023.02.044. Epub 2023 Sep 15. J Invest Dermatol. 2024. PMID: 37716648 Free article.
A novel mutation in FGFR2.
Goos JA, van den Ouweland AM, Swagemakers SM, Verkerk AJ, Hoogeboom AJ, van Veelen ML, Mathijssen IM, van der Spek PJ. Goos JA, et al. Among authors: hoogeboom aj. Am J Med Genet A. 2015 Jan;167A(1):123-7. doi: 10.1002/ajmg.a.36827. Epub 2014 Nov 25. Am J Med Genet A. 2015. PMID: 25425289
[Prenatally detected orofacial cleft].
Exalto N, Cohen-Overbeek TE, van Adrichem LN, Oudesluijs GG, Hoogeboom AJ, Wildschut HI. Exalto N, et al. Among authors: hoogeboom aj. Ned Tijdschr Geneeskd. 2009;153:B316. Ned Tijdschr Geneeskd. 2009. PMID: 19785790 Review. Dutch.
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
Genetic basis of alpha-aminoadipic and alpha-ketoadipic aciduria.
Hagen J, te Brinke H, Wanders RJ, Knegt AC, Oussoren E, Hoogeboom AJ, Ruijter GJ, Becker D, Schwab KO, Franke I, Duran M, Waterham HR, Sass JO, Houten SM. Hagen J, et al. Among authors: hoogeboom aj. J Inherit Metab Dis. 2015 Sep;38(5):873-9. doi: 10.1007/s10545-015-9841-9. Epub 2015 Apr 10. J Inherit Metab Dis. 2015. PMID: 25860818
PREPL deficiency: delineation of the phenotype and development of a functional blood assay.
Régal L, Mårtensson E, Maystadt I, Voermans N, Lederer D, Burlina A, Juan Fita MJ, Hoogeboom AJM, Olsson Engman M, Hollemans T, Schouten M, Meulemans S, Jonson T, François I, Gil Ortega D, Kamsteeg EJ, Creemers JWM. Régal L, et al. Among authors: hoogeboom ajm. Genet Med. 2018 Jan;20(1):109-118. doi: 10.1038/gim.2017.74. Epub 2017 Jul 20. Genet Med. 2018. PMID: 28726805 Free article.
Pfeiffer syndrome: the importance of prenatal diagnosis.
Nieuwenhuyzen-De Boer GM, Hoogeboom AJ, Smit LS, Heydanus R, Eggink AJ. Nieuwenhuyzen-De Boer GM, et al. Among authors: hoogeboom aj. Eur J Obstet Gynecol Reprod Biol. 2014 Oct;181:339-40. doi: 10.1016/j.ejogrb.2014.08.006. Epub 2014 Aug 13. Eur J Obstet Gynecol Reprod Biol. 2014. PMID: 25183684 No abstract available.
Phenotype and genotype in 103 patients with tricho-rhino-phalangeal syndrome.
Maas SM, Shaw AC, Bikker H, Lüdecke HJ, van der Tuin K, Badura-Stronka M, Belligni E, Biamino E, Bonati MT, Carvalho DR, Cobben J, de Man SA, Den Hollander NS, Di Donato N, Garavelli L, Grønborg S, Herkert JC, Hoogeboom AJ, Jamsheer A, Latos-Bielenska A, Maat-Kievit A, Magnani C, Marcelis C, Mathijssen IB, Nielsen M, Otten E, Ousager LB, Pilch J, Plomp A, Poke G, Poluha A, Posmyk R, Rieubland C, Silengo M, Simon M, Steichen E, Stumpel C, Szakszon K, Polonkai E, van den Ende J, van der Steen A, van Essen T, van Haeringen A, van Hagen JM, Verheij JB, Mannens MM, Hennekam RC. Maas SM, et al. Among authors: hoogeboom aj. Eur J Med Genet. 2015 May;58(5):279-92. doi: 10.1016/j.ejmg.2015.03.002. Epub 2015 Mar 16. Eur J Med Genet. 2015. PMID: 25792522
61 results