De novo variants in Myelin regulatory factor (MYRF) as candidates of a new syndrome of cardiac and urogenital anomalies. [electronic resource]
Producer: 20190228Description: 969-972 p. digitalISSN:- 1552-4833
- Alleles
- Child, Preschool
- Gene Frequency
- Genetic Association Studies
- Genetic Predisposition to Disease
- Genetic Variation
- Genotype
- Heart Defects, Congenital -- diagnosis
- Humans
- Male
- Membrane Proteins -- genetics
- Mutation
- Phenotype
- Syndrome
- Transcription Factors -- genetics
- Urogenital Abnormalities -- diagnosis
No physical items for this record
Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural
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