All individuals with variants in gene NUP37

2 entries on 1 page. Showing entries 1 - 2.
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00296692 NCG_00096 PubMed: Haskell 2017 - M - United States African American - - - - ? suspected short QT syndrome; arrhythmia, cardiomyopathy, atrial fibrillation, family history sudden cardiac death 1 1 Johan den Dunnen
00464291 patient PubMed: Tidwell 2020, Journal: Tidwell 2020 2-generation family, 1 affected, unaffected non carrier parents M no United States white;Peru;native American - - - - ? see paper; ..., microcephaly, severe global developmental delay; ventricular septal defect, patent foramen ovale, rhizomelic shortening extremities, pectus carinatum, underdeveloped genitalia (severe penoscrotal hypospadias, cryptorchidism); distinctive facial features, bulbous nasal tip, microretrognathia, downturned corners mouth 1 1 Johan den Dunnen
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