Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization. [electronic resource]
Producer: 20120209Description: 2754-61 p. digitalISSN:- 1552-4833
- Abnormal Karyotype
- Adolescent
- Child, Preschool
- Chromosome Deletion
- Chromosome Mapping
- Chromosomes, Human, Pair 20 -- genetics
- Chromosomes, Human, Pair 9 -- genetics
- Comparative Genomic Hybridization -- methods
- DNA Copy Number Variations
- Developmental Disabilities -- genetics
- Forkhead Transcription Factors -- genetics
- Genome, Human
- Guanine Nucleotide Exchange Factors -- genetics
- Humans
- In Situ Hybridization, Fluorescence
- Inheritance Patterns
- Intellectual Disability -- genetics
- Male
- Metaphase
- Physical Examination
- Trisomy -- diagnosis
No physical items for this record
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.