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Phenotype and genotype in 17 patients with Goltz-Gorlin syndrome.
Maas SM, Lombardi MP, van Essen AJ, Wakeling EL, Castle B, Temple IK, Kumar VK, Writzl K, Hennekam RC. Maas SM, et al. Among authors: hennekam rc. J Med Genet. 2009 Oct;46(10):716-20. doi: 10.1136/jmg.2009.068403. Epub 2009 Jul 7. J Med Genet. 2009. PMID: 19586929
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.
Further delineation of the Yunis-Varon syndrome.
Hennekam RC, Vermeulen-Meiners C. Hennekam RC, et al. J Med Genet. 1989 Jan;26(1):55-8. doi: 10.1136/jmg.26.1.55. J Med Genet. 1989. PMID: 2918527 Free PMC article.
Dermal eccrine cylindromatosis.
van Balkom ID, Hennekam RC. van Balkom ID, et al. Among authors: hennekam rc. J Med Genet. 1994 Apr;31(4):321-4. doi: 10.1136/jmg.31.4.321. J Med Genet. 1994. PMID: 8071959 Free PMC article. Review. No abstract available.
594 results