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Clinical Dysmorphology|March 2, 2013
Clinical phenotype and the lack of mutations in the CHRNG, CHRND, and CHRNA1 genes in two Indian families with Escobar syndromeSrinivas G Kodaganur, Sagar J Tontanahal, Astha Sarda, et al.Clinical Dysmorphology|December 6, 2012
Novel FGD1 mutation underlying Aarskog-Scott syndrome with myopathy and distal arthropathyAbdulaziz Al-Semari, Salma M Wakil, Mohammad A Al-Muhaizea, et al.Clinical Dysmorphology|April 17, 2012
Abraham Lincoln's marfanoid mother: the earliest known case of multiple endocrine neoplasia type 2B?John G SotosClinical Dysmorphology|November 28, 2012
Two patients with intellectual disability, overlapping facial features, and overlapping deletions in 6p25.1p24.3Bart C W Kuipers, Anneke T Vulto-van Silfhout, Carlo Marcelis, et al.Clinical Dysmorphology|December 5, 2013
A novel frameshift mutation and infrequent clinical findings in two cases with Dyggve-Melchior-Clausen syndromeMehmet Seven, Erkan Koparir, Alper Gezdirici, et al.Clinical Dysmorphology|January 1, 1995
Mandibulo-acral dysplasia: heterogeneity versus variabilityH V TorielloClinical Dysmorphology|January 1, 1995
Osteodysplastic primordial dwarfism: a case with features of type IIM Masuno, K Imaizumi, G Nishimura, et al.Clinical Dysmorphology|January 1, 1995
Mulibrey nanismS Balg, S Stengel-Rutkowski, C Döhlemann, et al.Clinical Dysmorphology|January 1, 1995
A child with oligo-syndactyly and 'apple peel' bowel atresiaJ A Cook, C BennettClinical Dysmorphology|January 1, 1995
'Disorganization-like syndrome' with 47,XXY and unilateral narrowing of the common iliac arteryC G Woods, S Treleaven, F R Betheras, et al.Pageof 117