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Plastic and Reconstructive Surgery|December 3, 2009
The natural history of patients treated for TWIST1-confirmed Saethre-Chotzen syndromeRoy Foo, Yifan Guo, Donna M McDonald-McGinn, et al.Clinical Genetics|April 1, 1986
Congenital heart disease in supernumerary der(22),t(11;22) syndromeA E Lin, J Bernar, A J Chin, et al.American Journal of Medical Genetics|February 15, 2001
Boy with bilateral retinoblastoma due to an unusual ring chromosome 13 with activation of a latent centromereJ D Morrissette, L Celle, N L Owens, et al.European Journal of Human Genetics : EJHG|April 18, 2003
Rearrangement in the PITX2 and MIPOL1 genes in a patient with a t(4;14) chromosomeDeepak Kamnasaran, Patricia C O'Brien, Elaine H Zackai, et al.American Journal of Medical Genetics|April 1, 1989
Clinical, cytogenetic, and pedigree findings in 18 cases of Aicardi syndromeA E Donnenfeld, R J Packer, E H Zackai, et al.American Journal of Medical Genetics|March 9, 1999
Aphallia as part of urorectal septum malformation sequence in an infant of a diabetic motherK W Gripp, M Barr, G Anadiotis, et al.American Journal of Medical Genetics|February 11, 1997
Diaphragmatic hernia-exomphalos-hypertelorism syndrome: a new case and further evidence of autosomal recessive inheritanceK W Gripp, D Donnai, C L Clericuzio, et al.American Journal of Medical Genetics. Part A|November 4, 2004
Symptomatic Chiari I malformation in Kabuki syndromeKaren L Ciprero, Jill Clayton-Smith, Dian Donnai, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 18, 2008
Parathyroid hormone reserve in 22q11.2 deletion syndromeChirag R Kapadia, Yuran E Kim, Donna M McDonald-McGinn, et al.Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|December 5, 2006
Ocular findings in the chromosome 22q11.2 deletion syndromeBrian J Forbes, Gil Binenbaum, Jane C Edmond, et al.Pageof 63