Expanding the clinical spectrum ofMYCN-related Feingold syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference9 articles.
1. Feingold syndrome: Clinical review and genetic mapping
2. Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay
3. Digital anomalies, microcephaly, and normal intelligence: New syndrome or Feingold syndrome?
4. Vertebral defects in a patient with Feingold syndrome
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1. Mycn regulates intestinal development through ribosomal biogenesis in a zebrafish model of Feingold syndrome 1;PLOS Biology;2022-11-01
2. Investigation of Submicroscopic Chromosomal Anomalies on Patients with Unexplained Intellectual Disabilities with Molecular Karyotyping;Gazi Medical Journal;2022-10-01
3. A new variant of MYCN gene as a cause of Feingold syndrome;Clinical Case Reports;2022-05
4. Prenatal detection of chromosomal abnormalities and copy number variants in fetuses with congenital gastrointestinal obstruction;BMC Pregnancy and Childbirth;2022-01-19
5. Genetic diagnoses in pediatric patients with epilepsy and comorbid intellectual disability;Epilepsy Research;2021-02
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