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Mutations in CCBE1 cause generalized lymph vessel dysplasia in humans.
Alders M, Hogan BM, Gjini E, Salehi F, Al-Gazali L, Hennekam EA, Holmberg EE, Mannens MM, Mulder MF, Offerhaus GJ, Prescott TE, Schroor EJ, Verheij JB, Witte M, Zwijnenburg PJ, Vikkula M, Schulte-Merker S, Hennekam RC. Alders M, et al. Among authors: hennekam rc, hennekam ea. Nat Genet. 2009 Dec;41(12):1272-4. doi: 10.1038/ng.484. Nat Genet. 2009. PMID: 19935664
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.
Further delineation of the partial proximal trisomy 10q syndrome.
Aalfs CM, Hoovers JM, Nieste-Otter MA, Mannens MM, Hennekam RC, Leschot NJ. Aalfs CM, et al. Among authors: hennekam rc. J Med Genet. 1995 Dec;32(12):968-71. doi: 10.1136/jmg.32.12.968. J Med Genet. 1995. PMID: 8825926 Free PMC article.
593 results