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Clinical Dysmorphology|October 18, 2003
Interstitial deletion of chromosome 2p16.2p21S R Sanders, A J Dawson, A Vust, et al.
Clinical Dysmorphology|October 18, 2003
Craniosynostosis associated with intracranial calcification: a novel recessive syndromeCheryl Longman, Margo Whiteford, David Koppel, et al.
Clinical Dysmorphology|October 18, 2003
Frontonasal dysplasia, Poland anomaly and unilateral hypoplasia of lower limb: report on a male patientMaria Leine Guion-Almeida, Vera Lúcia Gil da Silva Lopes
Clinical Dysmorphology|October 18, 2003
Catel-Manzke syndrome without cleft palate: a case reportRatna Dua Puri, Shubha R Phadke
Clinical Dysmorphology|October 18, 2003
Unusual combination of limb malformations in the same patient: brachydactyly with syndactyly and postaxial polydactyly of the hands and postaxial oligodactyly of the feetE Ferda Percin, Sarper Yilmaz
Clinical Dysmorphology|June 1, 2017
Pierpont syndrome: report of a new patientAnne-Karin Kahlert, Sabine Weidensee, Luisa Mackenroth, et al.
Clinical Dysmorphology|May 16, 2017
Novel OFD1 frameshift mutation in a Chinese boy with Joubert syndrome: a case report and literature reviewKaihui Zhang, Chen Meng, Jing Ma, et al.
Clinical Dysmorphology|July 10, 2018
Facial profile and additional features in fetuses with trisomy 21Periyasamy Radhakrishnan, Shalini S Nayak, Anju Shukla, et al.
Clinical Dysmorphology|May 29, 2009
Caudal duplication syndrome with unilateral hypoplasia of the pelvis and lower limb and ventriculoseptal heart defect in a mother and features of VATER association in her childKristin Becker, Karol Howard, Derek Klazinga, et al.
Clinical Dysmorphology|December 17, 2008
Two children with subtelomeric 11q deletions: a description and interpretation of their clinical presentations and molecular genetic findingsHelen Cox, Anneke Lucassen, Marlene Rio, et al.
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