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Clinical Dysmorphology|August 7, 2026
Monochorionic dizygotic twins with discordant genetic findings and congenital malformationsCaiqun Luo, Xiaoxia Wu, Yang Liu, et al.
Clinical Dysmorphology|October 5, 2010
Cantu syndrome and lymphoedemaDiana García-Cruz, Alejandra Mampel, Maria I Echeverria, et al.
Clinical Dysmorphology|June 26, 2010
A family with hereditary congenital facial paresis and a brief review of the literatureIsmail S Alrashdi, Philip Rich, Michael A Patton
Clinical Dysmorphology|August 31, 2010
Nicolaides-Baraitser syndrome: two new cases with autism spectrum disorderSimone Gana, Michela Panizzon, Daniela Fongaro, et al.
Clinical Dysmorphology|April 22, 2016
Mandibuloacral dysplasia and LMNA A529V mutation in Turkish patients with severe skeletal changes and absent breast developmentLeyla Ozer, Evrim Unsal, Suleyman Aktuna, et al.
Clinical Dysmorphology|February 17, 2016
A recurrent TP63 mutation causing EEC3 and Rapp-Hodgkin syndromesFelix B Brueggemann, Oliver Bartsch
Clinical Dysmorphology|February 18, 2016
Germline mosaicism in osteopathia striata with cranial sclerosis--recurrence in siblingsJames J O'Byrne, Ethna Phelan, Ellen Steenackers, et al.
Clinical Dysmorphology|August 20, 2019
SATB2-associated syndrome: first report of a gonadal and somatic mosaicism for an intragenic copy number variationMaude Grelet, Jérémie Mortreux, Emilie Alazard, et al.
Clinical Dysmorphology|October 3, 2019
Klippel-Feil syndrome: a review of the literatureRim Frikha
Clinical Dysmorphology|January 25, 2021
Distal arthrogryposis type 5D in a South Indian family caused by novel deletion in ECEL1 geneMamatha Gowda, Shruthi Mohan, Devika Ramesh, et al.
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