• A Case of Growth Hormone Use in Dyggve-Melchior-Clausen Syndrome
• A homozygous nonsense variant in DYM underlies Dyggve-Melchior-Clausen syndrome associated with ectodermal features
• A Novel Homozygous Frameshift Variant in <em>DYM</em> Causing Dyggve-Melchior-Clausen Syndrome in Pakistani Patients
• A Novel Homozygous Frameshift Variant in DYM Causing Dyggve-Melchior-Clausen Syndrome in Pakistani Patients
• A Novel Homozygous Nonsense Variant in the <em>DYM</em> Underlies Dyggve-Melchior-Clausen Syndrome in Large Consanguineous Family
• A Novel Homozygous Nonsense Variant in the DYM Underlies Dyggve-Melchior-Clausen Syndrome in Large Consanguineous Family
• An extremely rare association of dyggve-melchior-clausen syndrome with mania: coincidence or comorbidity
• Atlantoaxial Instability Treated with Posterior Atlantoaxial Fixation in Two Siblings with Dyggve-Melchior-Clausen Syndrome
• Bilateral Severe Genu Varum in Dyggve-Melchior-Clausen Syndrome - A Case Report
• Case Report: Precision genetic diagnosis in a case of Dyggve-Melchior-Clausen syndrome reveals paternal isodisomy and heterodisomy of chromosome 18 with imprinting clinical implications
• Clinical and genetic analysis of a Chinese pedigree affected with Dyggve-Melchior-Clausen syndrome due to a novel frameshift variant of DYM gene
• Clinical, radiological and molecular studies in 24 individuals with Dyggve-Melchior-Clausen dysplasia and Smith-McCort dysplasia from India
• Dyggve-Melchior-Clausen Syndrome Caused by a Novel Frameshift Variant in a Japanese Patient
• Dyggve-Melchiore-Clausen dysplasia (DMC): syndrome associated with a micropenis
• Dymeclin deficiency causes postnatal microcephaly, hypomyelination and reticulum-to-Golgi trafficking defects in mice and humans
• Perinatal Diagnostic Approach to Fetal Skeletal Dysplasias: Six Years Experience of a Tertiary Center
• Re: Propofol in Triple Trouble Kearns-Sayre Syndrome, Dyggve-Melchior-Clausen Syndrome, and Chromosome-9 Inversion
• The family reported to have X-linked Dyggve-Melchior-Clausen syndrome instead has X-linked SEDT caused by a novel TRAPPC2 frameshift variant
• Total Hip Arthroplasty in Dyggve-Melchior-Clausen Syndrome: Literature Review and Case Report