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Rubinstein-Taybi syndrome in The Netherlands.
Hennekam RC, Van Den Boogaard MJ, Sibbles BJ, Van Spijker HG. Hennekam RC, et al. Among authors: van spijker hg, van den boogaard mj. Am J Med Genet Suppl. 1990;6:17-29. doi: 10.1002/ajmg.1320370604. Am J Med Genet Suppl. 1990. PMID: 2118773
A cephalometric study in Rubinstein-Taybi syndrome.
Hennekam RC, Van den Boogaard MJ, Van Doorne JM. Hennekam RC, et al. Among authors: van den boogaard mj, van doorne jm. J Craniofac Genet Dev Biol. 1991 Jan-Mar;11(1):33-40. J Craniofac Genet Dev Biol. 1991. PMID: 2061404
Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3.
Breuning MH, Dauwerse HG, Fugazza G, Saris JJ, Spruit L, Wijnen H, Tommerup N, van der Hagen CB, Imaizumi K, Kuroki Y, van den Boogaard MJ, de Pater JM, Mariman EC, Hamel BC, Himmelbauer H, Frischauf AM, Stallings R, Beverstock GC, van Ommen GJ, Hennekam RC. Breuning MH, et al. Among authors: van den boogaard mj, van ommen gj, van der hagen cb. Am J Hum Genet. 1993 Feb;52(2):249-54. Am J Hum Genet. 1993. PMID: 8430691 Free PMC article.
The Peters'-Plus syndrome: description of 16 patients and review of the literature.
Hennekam RC, Van Schooneveld MJ, Ardinger HH, Van Den Boogaard MJ, Friedburg D, Rudnik-Schoneborn S, Seguin JH, Weatherstone KB, Wittebol-Post D, Meinecke P. Hennekam RC, et al. Among authors: van schooneveld mj, van den boogaard mj. Clin Dysmorphol. 1993 Oct;2(4):283-300. Clin Dysmorphol. 1993. PMID: 7508316 Review.
Etiology and pathogenesis of robin sequence in a large Dutch cohort.
Basart H, Paes EC, Maas SM, van den Boogaard MJ, van Hagen JM, Breugem CC, Cobben JM, Don Griot JP, Lachmeijer AM, Lichtenbelt KD, van Nunen DP, van der Horst CM, Hennekam RC. Basart H, et al. Among authors: van der horst cm, van den boogaard mj, van hagen jm, van nunen dp. Am J Med Genet A. 2015 Sep;167A(9):1983-92. doi: 10.1002/ajmg.a.37154. Epub 2015 May 31. Am J Med Genet A. 2015. PMID: 26033782
76 results