A report of 2 cases of Cornelia de Lange syndrome (CdLS) and an analysis of clinical and genetic characteristics in a Chinese CdLS cohort - Li - 2020 - Molecular Genetics &
Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement | Nature Reviews Genetics
Two novel RAD21 mutations in patients with mild Cornelia de Lange syndrome-like presentation and report of the first familial case - ScienceDirect
Cornelia de Lange syndrome: Clinical review, diagnostic and scoring systems, and anticipatory guidance - Kline - 2007 - American Journal of Medical Genetics Part A - Wiley Online Library
Diagnostico prenatal en Sindrome de Cornelia de Lange a propósito de 2 casos
Atteinte du syndrome de Cornelia de Lange: Waiza, bébé miracle
Cornelia de Lange Sendromu: İki Olgu - Yeni Tıp Dergisi
Frontiers | Case report: A novel case of parental mosaicism in SMC1A gene causes inherited Cornelia de Lange syndrome
Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement. - Abstract - Europe PMC
Diagnosis and management of Cornelia de Lange Syndrome: first international consensus statement (Adapted for easy access and wid
Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype–phenotype correlations and common mechanisms - Kaur - 2023 - American Journal of Medical Genetics Part A - Wiley Online Library
Cornelia de Lange syndrome: MedlinePlus Genetics
Diagnostico prenatal en Sindrome de Cornelia de Lange a propósito de 2 casos
Residência Pediátrica - Síndrome de Cornélia de Lange: relato de caso
Cornelia de Lange individuals with new and recurrent SMC1A mutations enhance delineation of mutation repertoire and phenotypic spectrum - Gervasini - 2013 - American Journal of Medical Genetics Part A - Wiley Online Library
Isolated NIBPL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction | European Journal of Human Genetics
Frontiers | Case Report: Novel NIPBL Variants Cause Cornelia de Lange Syndrome in Chinese Patients
Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement | Nature Reviews Genetics
Diagnostics | Free Full-Text | A Broader Perspective on the Prenatal Diagnosis of Cornelia de Lange Syndrome: Review of the Literature and Case Presentation
Syndrome de Cornelia de Lange — Wikipédia
View of Survey of anesthetic and airway management in children and adults with Cornelia de Lange syndrome: parents' perceptions and perspectives | Anaesthesia, Pain & Intensive Care
Síndrome de Cornelia de Lange | uDocz
A novel nonsense SMC1A mutation in a patient with intractable epilepsy and cardiac malformation | Human Genome Variation
Behavioural phenotype of Cornelia de Lange syndrome: case–control study | The British Journal of Psychiatry | Cambridge Core
Genes | Free Full-Text | Cornelia de Lange Syndrome: From a Disease to a Broader Spectrum
