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Clinical Dysmorphology|April 18, 2009
Confirmation of microcephaly-facio-cardio-skeletal Hadziselimovic type syndromeBruno Dallapiccola, Maria Cristina Digilio, Adriana Zatterale, et al.Clinical Dysmorphology|February 25, 2010
Congenital heart defects in two siblings in an Axenfeld-Rieger syndrome familyMehmet Necdet Akkus, Atilla ArginClinical Dysmorphology|August 31, 2016
Metaphyseal dysplasia, Spahr type; missense MMP13 mutations in two Iraqi siblingsShereen Tadros, Richard H Scott, Alistair D Calder, et al.Clinical Dysmorphology|December 30, 2009
Amniotic bands in paternal half-siblingsMoira Blyth, Katherine LachlanClinical Dysmorphology|December 1, 2005
Supernumerary marker chromosome 7 and maternal uniparental disomy 7 in a boy with growth retardation and triangular faceThomas Eggermann, Ines Krause-Plonka, Hartmut A Wollmann, et al.Clinical Dysmorphology|December 1, 2005
Description of a new syndrome: auricular abnormalities and cleft lip in two sibs, in association with cleft palate and unusual opthalmological findingsHelen R Murphy, Janet Birch, Claire Brooks, et al.Clinical Dysmorphology|June 19, 2018
Familial impairment of vocal cord mobility in childhood with clubfootRebecca Shaw, Cristina Dias, Jeffrey Ludemann, et al.Clinical Dysmorphology|January 1, 1992
Multisystem disorder of Punjabi children exhibiting spontaneous dermal and submucosal granulation tissue formation: LOGIC syndromeJ R Ainsworth, G Shabbir, A F Spencer, et al.Clinical Dysmorphology|January 1, 1992
Encephalocele, radial defects, cardiac, gastrointestinal, anal, and renal anomalies: a new multiple congenital anomaly (MCA) syndrome?U Froster-Iskenius, P MeineckeClinical Dysmorphology|July 1, 1992
Chondrodysplasia punctata: further evidence of heterogeneityA M Norman, S Jivani, H M KingstonPageof 117