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Clinical Dysmorphology|September 8, 2006
Patient with novel interstitial deletion of chromosome 3q13.1q13.3 and agenesis of the corpus callosumAmy Lawson-Yuen, Sue Ann Berend, Janet S Soul, et al.Clinical Dysmorphology|September 8, 2006
Interstitial deletion of the short arm of chromosome 2 in a mother and child, with facial dysmorphism and mild learning difficultiesRuth Armstrong, Ian Ellis, Catherine Kightley, et al.Clinical Dysmorphology|September 8, 2006
Neuhauser syndrome and Peters' anomalyCoskun Yarar, Ayten Yakut, Nilgun Yildirim, et al.Clinical Dysmorphology|August 4, 2009
Dysmorphology of Barth syndromeRob Hastings, Colin Steward, Beverly Tsai-Goodman, et al.Clinical Dysmorphology|March 14, 2009
Trisomy 9p and Prader-Willi syndromes in an infant resulting from a de-novo unbalanced t(9;15) translocationMelissa T Carter, Francois D Jacob, Elizabeth Sinclair-Bourque, et al.Clinical Dysmorphology|December 6, 2008
Two brothers with a microduplication including the MECP2 gene: rapid head growth in infancy and resolution of susceptibility to infectionTrine E Prescott, Olaug K Rødningen, Alf Bjørnstad, et al.Clinical Dysmorphology|March 24, 2009
Oculoauriculovertebral spectrum: report of nine familial cases with evidence of autosomal dominant inheritance and review of the literatureSiulan Vendramini-Pittoli, Nancy Mizue Kokitsu-NakataClinical Dysmorphology|July 21, 2009
Congenital anterolateral bowing of the tibia with ipsilateral polydactyly of the great toe associated with cerebral cyst: a new entity?Jeroen Breckpot, Bernard Thienpont, Christine Vanhole, et al.Clinical Dysmorphology|December 4, 2008
Sudden death in spondylo-meta-epiphyseal dysplasia, short limb-abnormal calcification typeCristina Dias, Robyn Cairns, Millan S PatelClinical Dysmorphology|December 4, 2008
Spondylo-meta-epiphyseal dysplasia, short limb-abnormal calcification typeSarah F Smithson, David Grier, Christine M HallPageof 117