A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed as Opitz-C: Similarities Between Schaaf-Yang and Opitz-C Syndromes | Scientific Reports
Opitz Trigonocephaly Syndrome | SpringerLink
Stickler Syndrome: Causes, Effects, and Treatment Options
Apert Syndrome: Practice Essentials, Pathophysiology, Epidemiology
Infant Recovers from COVID-19, Fights Related Syndrome MIS-C
Craniofrontonasal syndrome. Hypertelorism, divergent squint, central... | Download Scientific Diagram
Cri du chat syndrome - Wikipedia
Genes | Free Full-Text | From Genotype to Phenotype—A Review of Kabuki Syndrome
Cureus | A Case of Early Diagnosis of Turner Syndrome in a Neonate | Article
Genes | Free Full-Text | Clinical Manifestations in a Girl with NAA10-Related Syndrome and Genotype–Phenotype Correlation in Females
Frontiers | Case Report: MIS-C Temporarily Associated With COVID-19 Complicated by Reye's Syndrome
Indian Pediatrics - Editorial
Multisystem Inflammatory Syndrome in Children (MIS-C)
Cockayne syndrome - Wikipedia
Skin Symptoms in Most Children with Multi-System Inflammatory Syndrome Related to COVID-19 – Consult QD
Coffin–Lowry syndrome | European Journal of Human Genetics
MIS-C and COVID-19: Uncommon but Serious Inflammatory Syndrome in Kids and Teens | Johns Hopkins Medicine
C syndrome with skeletal anomalies, mental retardation, eyelid chalazion, Bitot's spots and agenesis of the corpus callosum in an Egyptian child - ScienceDirect
Genes | Free Full-Text | Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review
Rubinstein–Taybi syndrome - Wikipedia
Clinical and Mutation Spectra of Cockayne Syndrome in India Narayanan DL, Tuteja M, McIntyre AD, Hegele RA, Calmels N, Obringer C, Laugel V, Mandal K, Phadke SR Neurol India
Screening of CD96 and ASXL1 in 11 patients with Opitz C or Bohring–Opitz syndromes - Urreizti - 2016 - American Journal of Medical Genetics Part A - Wiley Online Library
Multisystem inflammatory syndrome in children (MIS-C)
MN1 C-terminal truncation syndrome: MedlinePlus Genetics
C syndrome with skeletal anomalies, mental retardation, eyelid chalazion, Bitot's spots and agenesis of the corpus callosum in an Egyptian child - ScienceDirect
Metopic and sagittal synostosis in Greig cephalopolysyndactyly syndrome: five cases with intragenic mutations or complete deletions of GLI3 | European Journal of Human Genetics
