Molecular cytogenetic characterization of a subtle interstitial del(3)(p25.3p26.2) in a patient with deletion 3p syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference20 articles.
1. CALL gene is haploinsufficient in a 3p? syndrome patient
2. Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome.
3. Detailed mapping of a congenital heart disease gene in chromosome 3p25
4. A second patient with partial deletion of the short arm of chromosome 3: karyotype 46,XY,del(3)(p25).
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2. Adapted whole‐body surveillance for von Hippel–Lindau‐associated tumors in 3p deletion syndrome with VHL deletion: A case report;Pediatric Blood & Cancer;2022-04-19
3. De novo 3p25-deletiós szindróma genotípus-fenotípus vizsgálata;Orvosi Hetilap;2022-03-20
4. Molecular Genetic Analysis of Newborns with Congenital Microcephaly;Neonatology;2022
5. Familiar del3p syndrome: The uncertainty of the prognosis. A case report;Clinical Case Reports;2021-03-09
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