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Holoprosencephaly: the Maastricht experience.
Moog U, De Die-Smulders CE, Schrander-Stumpel CT, Engelen JJ, Hamers AJ, Frints S, Fryns JP. Moog U, et al. Genet Couns. 2001;12(3):287-98. Genet Couns. 2001. PMID: 11693794
Acampomelic campomelic syndrome.
Moog U, Jansen NJ, Scherer G, Schrander-Stumpel CT. Moog U, et al. Am J Med Genet. 2001 Dec 1;104(3):239-45. Am J Med Genet. 2001. PMID: 11754051
Chromosome bands and ends revisited.
Moog U, Engelen JJ, Schrander-Stumpel CT, Fryns JP. Moog U, et al. Am J Med Genet A. 2003 Aug 15;121A(1):88-9. doi: 10.1002/ajmg.a.20153. Am J Med Genet A. 2003. PMID: 12900910 No abstract available.
Rett syndrome in females with CTS hot spot deletions: a disorder profile.
Smeets E, Terhal P, Casaer P, Peters A, Midro A, Schollen E, van Roozendaal K, Moog U, Matthijs G, Herbergs J, Smeets H, Curfs L, Schrander-Stumpel C, Fryns JP. Smeets E, et al. Among authors: moog u. Am J Med Genet A. 2005 Jan 15;132A(2):117-20. doi: 10.1002/ajmg.a.30410. Am J Med Genet A. 2005. PMID: 15578576
140 results