Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization. [electronic resource]
- American journal of medical genetics. Part A Nov 2011
- 2754-61 p. digital
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
1552-4833
10.1002/ajmg.a.34168 doi
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