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Clinical Dysmorphology|November 4, 2008
Macrocephaly-cutis marmorata telangiectatica congenita: a report on the natural history of a mild caseNatalie L E Canham, Susan E HolderClinical Dysmorphology|April 3, 2009
A review of prenatally detected femoral abnormalitiesRuth Armstrong, Emma McCann, Alan Fryer, et al.Clinical Dysmorphology|March 14, 2007
Two cases of macrocephaly and immune deficiencyOzgur Cogulu, Ayca Aykut, Necil Kutukculer, et al.Clinical Dysmorphology|March 14, 2007
Interstitial deletion of the short arm of chromosome 1 (1p13.1p21.1) in a girl with mental retardation, short stature and colobomataAnne-Marie Bisgaard, Leif Normann Rasmussen, Hans Ulrik Møller, et al.Clinical Dysmorphology|March 14, 2007
Cerebro-facio-thoracic dysplasia: expanding the phenotypeDeirdre Cilliers, Yasemin Alanay, Koray Boduroglu, et al.Clinical Dysmorphology|August 27, 2009
Clinical spectrum of Bardet-Biedl syndrome among four Saudi Arabian familiesMathew Punnachalil Cherian, Nouriya A Al-Sanna'aClinical Dysmorphology|April 9, 2010
Familial microhydranencephaly, a family that does not map to 16p13.13-p12.2: relationship with hereditary fetal brain degeneration and fetal brain disruption sequenceJana Behunova, Eva Zavadilikova, Tarik M Bozoglu, et al.Clinical Dysmorphology|March 4, 2011
A novel heterozygous missense mutation G316D of SIX3 gene in a Brazilian patient with holoprosencephaly-like phenotype and Langerhans cell histiocytosisLucilene Arilho Ribeiro, Claudia Danielli Pereira Bertolacini, Rodrigo Gonçalves Quiezi, et al.Clinical Dysmorphology|November 9, 2011
Bilateral hand malformations with absence of carpal bones with fusion of proximal metacarpalsRavindra Muralidhar Gurav, Annasaheb B PatilClinical Dysmorphology|September 30, 2011
Floating-Harbor Syndrome: report on a case in a mother and daughter, further evidence of autosomal dominant inheritanceStéphanie Arpin, Alexandra Afenjar, Béatrice Dubern, et al.Pageof 117