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Clinical Dysmorphology|May 3, 2019
Chromosome 1q31.2q32.1 deletion in an adult male with intellectual disability, dysmorphic features and obesityZerin Hyder, Adele Fairclough, Sofia DouzgouClinical Dysmorphology|August 23, 2016
A probable new syndrome with the storage disease phenotype caused by the VPS33A gene mutationAli Dursun, Dilek Yalnizoglu, Omer F Gerdan, et al.Clinical Dysmorphology|March 8, 2022
Clinical implications of mosaicism: a 10-year retrospective review of 83 families in a university-affiliated genetics clinicMianne Lee, Adrian C Y Lui, Christopher C Y Mak, et al.Clinical Dysmorphology|October 26, 1999
A second family with Micro syndromeG Rodríguez Criado, M Rufo, I Gómez de TerrerosClinical Dysmorphology|October 26, 1999
Familial association of camptodactyly, mental retardation, whistling face and Pierre Robin sequenceC Stoll, F Benoit, M O Peter, et al.Clinical Dysmorphology|October 26, 1999
Jeune syndrome (asphyxiating thoracic dystrophy) associated with Hirschsprung diseaseP Aurora, C E WallisClinical Dysmorphology|October 26, 1999
Non-ossifying fibromas and giant cell reparative granulomas in a child with ocular-ectodermal syndromeH V Toriello, R Bultman, R W Panek, et al.Clinical Dysmorphology|October 26, 1999
A child with hemimegalencephaly, hemihypertrophy, macrocephaly, cutaneous vascular malformation, psychomotor retardation and intestinal lymphangiectasia--a diagnostic dilemmaM K Thong, E Thompson, R Keenan, et al.Clinical Dysmorphology|August 24, 1999
Oral-facial-digital syndrome with acromelic short stature: a new variant--overlap with Ellis Van Creveld syndromeS R Phadke, J Pahi, A Pandey, et al.Clinical Dysmorphology|August 24, 1999
Dominant inheritance of cleft palate with minor abnormalities of hands and feet: a new syndrome?E P Kirk, M WilsonPageof 117