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Pedigree of the DMC family in which homozygous insertion variant
Frontiers A Novel Homozygous Frameshift Variant in DYM Causing Dyggve-Melchior-Clausen Syndrome in Pakistani Patients
Children who harbor more than one P/LP variant. (A) Girl who inherited
Skeletal Dysplasias
Figure 3 from Spondylo-epi-metaphyseal dysplasia.
Dyggve-Melchior-Clausen Syndrome - DoveMed
Morquio Syndrome (Mucopolysaccharidosis Type IV) Differential Diagnoses
Flowchart of the approach used in this study to investigate a group of
Characteristics of Down syndrome – Littlest Warrior
PDF) Dyggve-Melchior-Clausen Syndrome
PDF) Dyggve–Melchior–Clausen syndrome without mental retardation (Smith–McCort dysplasia)
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