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Clinical Dysmorphology|January 31, 2014
Combined TSC1 and LMX1B mutations in a single patientOla Khalifa, Nadia Al-Sakati, Khalid Al-Mane, et al.Clinical Dysmorphology|June 22, 2011
Homozygous mutation of CRLF-1 gene in a Turkish newborn with Crisponi syndromeHese Cosar, Zelal Kahramaner, Aydin Erdemir, et al.Clinical Dysmorphology|October 1, 2011
Isolated macrodystrophia lipomatosa of the foot in a neonate: a case reportNilufer Guzoglu, Tulin Gokmen, Suna Serife Oguz, et al.Clinical Dysmorphology|October 1, 2011
Well-defined clinical presentation of Ehlers-Danlos syndrome in patients with tenascin-X deficiency: a report of four casesAnke G M Hendriks, Nicol C Voermans, Joost Schalkwijk, et al.Clinical Dysmorphology|July 16, 2011
A photographic essay of prolidase deficiencyRebecca Dunn, George Varigos, Ingrid WinshipClinical Dysmorphology|September 22, 2011
Blepharophimosis-ptosis-epicanthus inversus syndrome plus: deletion 3q22.3q23 in a patient with characteristic facial features and with genital anomalies, spastic diplegia, and speech delayStacy Zahanova, Brandon Meaney, Beata Łabieniec, et al.Clinical Dysmorphology|December 7, 2011
Terminal 14q deletion with unbalanced t(Y;14)(q12;q32) translocationGülseren Bağcı, Gökhan Ozan Çetin, Nur Semerci, et al.Clinical Dysmorphology|October 5, 2011
Pycnodysostosis with craniosynostosis: case report of the craniofacial and oral featuresHugo P Caracas, Paulo S Figueiredo, Heliana Dantas Mestrinho, et al.Clinical Dysmorphology|May 29, 2009
The phenotypic spectrum of trisomy 2: report of two new casesErcan Mihci, Gopalrao V N Velagaleti, Regina Ensenauer, et al.Clinical Dysmorphology|May 19, 2009
Fryns-Aftimos syndrome with milder clinical manifestationsIan M Hayes, David Perry, Salim AftimosPageof 117