A de novo interstitial deletion of 7q31.2q31.31 identified in a girl with developmental delay and hearing loss. [electronic resource]
Producer: 20171003Description: 102-8 p. digitalISSN:- 1552-4876
- Carrier Proteins -- genetics
- Child, Preschool
- Chromosome Deletion
- Chromosomes, Human, Pair 7 -- genetics
- Cystic Fibrosis Transmembrane Conductance Regulator -- genetics
- Developmental Disabilities -- genetics
- Female
- Genome, Human
- Hearing Loss, Sensorineural -- genetics
- Humans
- Membrane Transport Proteins
- N-Terminal Acetyltransferase C -- genetics
- Nerve Tissue Proteins -- genetics
- Nuclear Proteins
- Polymorphism, Single Nucleotide
- Proteins -- genetics
- Ribonucleoprotein, U4-U6 Small Nuclear -- genetics
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Publication Type: Case Reports; Journal Article
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