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Clinical Dysmorphology|February 1, 2022
Clinical and genetic studies of thiamine metabolism dysfunction syndrome-4: case series and review of the literatureBahadir M Samur, Gülsüm Gümüş, Mehmet Canpolat, et al.Clinical Dysmorphology|March 8, 2022
Uniparental disomy as a mechanism for X-linked chondrodysplasia punctataEmily Woods, Michael Yates, Farah Kanani, et al.Clinical Dysmorphology|March 8, 2022
"Laurin-Sandrow Syndrome - a review of the literature and classification system"Cezar Buzea, Nathalie BoulangerClinical Dysmorphology|October 26, 1999
Expanding the phenotype of Filippi syndrome: a report of three casesI R Walpole, T Parry, J GoldblattClinical Dysmorphology|October 26, 1999
Recurrence of the severe form of microgastria-limb reduction defect in a consanguineous familyL I al-Gazali, M Bakir, A Dawodu, et al.Clinical Dysmorphology|October 26, 1999
Aortic dissection, patent ductus arteriosus, iris hypoplasia and brachytelephalangy in a male adolescentL C Adès, R Davies, E A Haan, et al.Clinical Dysmorphology|October 26, 1999
Disorganisation: a case with popliteal pterygia and placental-skin appendagesL Korniszewski, A Skorka, D DonnaiClinical Dysmorphology|October 26, 1999
A girl with ectodermal dysplasia, choanal atresia and polysyndactylyA Slavotinek, J Clayton-SmithClinical Dysmorphology|October 26, 1999
Bilateral hydronephrosis due to megacalicosis as a prenatal sonographic finding in a female with Schinzel-Giedion syndromeO Rittinger, P Weiss-Wichert, G HasenöhrlClinical Dysmorphology|October 26, 1999
Syndrome of psychomotor retardation, bulbous nose, and epilepsy (Hernandez syndrome): a Brazilian caseD G Melo, A X Acosta, J M de Pina-NetoPageof 117