Clinical and molecular characterization of the first familial report of 1p32 microdeletion. [electronic resource]
Producer: 20180903Description: 36-41 p. digitalISSN:- 1473-5717
- Abnormalities, Multiple -- genetics
- Adult
- Chromosome Deletion
- Chromosomes, Human, Pair 1 -- genetics
- Comparative Genomic Hybridization
- DNA-Binding Proteins -- genetics
- Developmental Disabilities -- genetics
- Female
- Humans
- LDL-Receptor Related Proteins -- genetics
- Male
- Microcephaly -- genetics
- Pedigree
- Phenotype
- Transcription Factors -- genetics
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Publication Type: Journal Article
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