Disease: Oculodigitoesophagoduodenal syndrome
- A case of Feingold type 2 syndrome associated with keratoconus refines keratoconus type 7 locus on chromosome 13q
- A de novo 13q31.3 microduplication encompassing the miR-17 ~ 92 cluster results in features mirroring those associated with Feingold syndrome 2
- A de novo 4.4-Mb microdeletion in 2p24.3 → p24.2 in a girl with bilateral hearing impairment, microcephaly, digit abnormalities and Feingold syndrome
- A fourth case of Feingold syndrome type 2: psychiatric presentation and management
- A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1
- A Novel MYCN Variant Associated with Intellectual Disability Regulates Neuronal Development
- An allelic series of miR-17 ∼ 92-mutant mice uncovers functional specialization and cooperation among members of a microRNA polycistron
- Association esophageal atresia type 3 - microcephaly: an incomplete Feingold syndrome?
- c-myc and N-myc promote active stem cell metabolism and cycling as architects of the developing brain
- Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype
- De novo 13q31.1-q32.1 interstitial deletion encompassing the miR-17-92 cluster in a patient with Feingold syndrome-2
- Dissection of the MYCN locus in Feingold syndrome and isolated oesophageal atresia
- Distinct molecular pathways mediate Mycn and Myc-regulated miR-17-92 microRNA action in Feingold syndrome mouse models
- Features of Feingold syndrome 1 dominate in subjects with 2p deletions including MYCN
- Feingold Syndrome 1
- Feingold syndrome type 1: a rare cause of fetal microcephaly (prenatal diagnosis)
- Feingold syndrome type 2 in a patient from China
- Feingold syndrome: report of a new family and review
- Gain-of-function MYCN causes a megalencephaly-polydactyly syndrome manifesting mirror phenotypes of Feingold syndrome
- GENETIC COUNSELLING IN FEINGOLD SYNDROME AND A NOVEL MUTATION
- Genetic factors in isolated and syndromic esophageal atresia
- Genome sequencing identifies three molecular diagnoses including a mosaic variant in the <em>COL2A1</em> gene in an individual with Pol III-related leukodystrophy and Feingold syndrome
- Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans
- Growth deficiency in oculodigitoesophagoduodenal (Feingold) syndrome--case report and review of the literature
- Growth hormone deficiency, aortic dilation, and neurocognitive issues in Feingold syndrome 2
- How many entities exist for the spectrum of disorders associated with brachydactyly, syndactyly, short stature, microcephaly, and intellectual disability?
- Metacarpophalangeal pattern profile analysis for a 3-month-old infant with Feingold syndrome 2
- Mycn regulates intestinal development through ribosomal biogenesis in a zebrafish model of Feingold syndrome 1
- Neurobehavioral Alterations in a Genetic Murine Model of Feingold Syndrome 2
- Public preparation of out-moded medicaments: theriaca
- Vertebral anomalies in a new family with ODED syndrome