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Three new families with arterial tortuosity syndrome.
Am J Med Genet A. 2004 Dec 1;131(2):134-43. doi: 10.1002/ajmg.a.30272.
Am J Med Genet A. 2004.
PMID: 15529317
Autosomal dominant inheritance of left ventricular outflow tract obstruction.
Wessels MW, Berger RM, Frohn-Mulder IM, Roos-Hesselink JW, Hoogeboom JJ, Mancini GS, Bartelings MM, Krijger Rd, Wladimiroff JW, Niermeijer MF, Grossfeld P, Willems PJ.
Wessels MW, et al. Among authors: hoogeboom jj.
Am J Med Genet A. 2005 Apr 15;134A(2):171-9. doi: 10.1002/ajmg.a.30601.
Am J Med Genet A. 2005.
PMID: 15712195
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Limb anomalies in patients with CHARGE syndrome: an expansion of the phenotype.
Van de Laar I, Dooijes D, Hoefsloot L, Simon M, Hoogeboom J, Devriendt K.
Van de Laar I, et al.
Am J Med Genet A. 2007 Nov 15;143A(22):2712-5. doi: 10.1002/ajmg.a.32008.
Am J Med Genet A. 2007.
PMID: 17937444
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Diploid/triploid mosaicism in dysmorphic patients.
van de Laar I, Rabelink G, Hochstenbach R, Tuerlings J, Hoogeboom J, Giltay J.
van de Laar I, et al.
Clin Genet. 2002 Nov;62(5):376-82. doi: 10.1034/j.1399-0004.2002.620504.x.
Clin Genet. 2002.
PMID: 12431252
Review.
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Familial gigantism caused by an NSD1 mutation.
van Haelst MM, Hoogeboom JJ, Baujat G, Brüggenwirth HT, Van de Laar I, Coleman K, Rahman N, Niermeijer MF, Drop SL, Scambler PJ.
van Haelst MM, et al. Among authors: hoogeboom jj.
Am J Med Genet A. 2005 Nov 15;139(1):40-4. doi: 10.1002/ajmg.a.30973.
Am J Med Genet A. 2005.
PMID: 16222665
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X-linked recessive inheritance of radial ray deficiencies in a family with four affected males.
Galjaard RJ, Kostakoglu N, Hoogeboom JJ, Breedveld GJ, van der Linde HC, Hovius SE, Oostra BA, Sandkuijl LA, Akarsu AN, Heutink P.
Galjaard RJ, et al. Among authors: hoogeboom jj.
Eur J Hum Genet. 2001 Sep;9(9):653-8. doi: 10.1038/sj.ejhg.5200692.
Eur J Hum Genet. 2001.
PMID: 11571552
Review.
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Benign hereditary chorea of early onset maps to chromosome 14q.
de Vries BB, Arts WF, Breedveld GJ, Hoogeboom JJ, Niermeijer MF, Heutink P.
de Vries BB, et al. Among authors: hoogeboom jj.
Am J Hum Genet. 2000 Jan;66(1):136-42. doi: 10.1086/302725.
Am J Hum Genet. 2000.
PMID: 10631144
Free PMC article.
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