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583 results
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Page 1
Oculoauriculovertebral spectrum and cerebral anomalies.
Schrander-Stumpel CT, de Die-Smulders CE, Hennekam RC, Fryns JP, Bouckaert PX, Brouwer OF, da Costa JJ, Lommen EJ, Maaswinkel-Mooy PD. Schrander-Stumpel CT, et al. Among authors: hennekam rc. J Med Genet. 1992 May;29(5):326-31. doi: 10.1136/jmg.29.5.326. J Med Genet. 1992. PMID: 1583660 Free PMC article. Review.
Hereditary multiple exostoses.
Hennekam RC. Hennekam RC. J Med Genet. 1991 Apr;28(4):262-6. doi: 10.1136/jmg.28.4.262. J Med Genet. 1991. PMID: 1856833 Free PMC article. No abstract available.
Short rib syndrome--Beemer type in sibs.
Hennekam RC. Hennekam RC. Am J Med Genet. 1991 Aug 1;40(2):230-3. doi: 10.1002/ajmg.1320400221. Am J Med Genet. 1991. PMID: 1897578 Review.
A family with severe X-linked arthrogryposis.
Hennekam RC, Barth PG, Van Lookeren Campagne W, De Visser M, Dingemans KP. Hennekam RC, et al. Eur J Pediatr. 1991 Jul;150(9):656-60. doi: 10.1007/BF02072628. Eur J Pediatr. 1991. PMID: 1915520 Review.
A cephalometric study in Rubinstein-Taybi syndrome.
Hennekam RC, Van den Boogaard MJ, Van Doorne JM. Hennekam RC, et al. J Craniofac Genet Dev Biol. 1991 Jan-Mar;11(1):33-40. J Craniofac Genet Dev Biol. 1991. PMID: 2061404
Rubinstein-Taybi syndrome in The Netherlands.
Hennekam RC, Van Den Boogaard MJ, Sibbles BJ, Van Spijker HG. Hennekam RC, et al. Am J Med Genet Suppl. 1990;6:17-29. doi: 10.1002/ajmg.1320370604. Am J Med Genet Suppl. 1990. PMID: 2118773
583 results