Advanced bone age in a girl with Wiedemann-Steiner syndrome and an exonic deletion in KMT2A (MLL). [electronic resource]
- American journal of medical genetics. Part A Aug 2014
- 2079-83 p. digital
Publication Type: Case Reports; Journal Article
1552-4833
10.1002/ajmg.a.36590 doi
Abnormalities, Multiple--diagnosis Bone Diseases, Developmental--genetics Child, Preschool Comparative Genomic Hybridization DNA Copy Number Variations Exons Facies Female Hand--diagnostic imaging Heterozygote Humans Myeloid-Lymphoid Leukemia Protein--genetics Phenotype Radiography Sequence Deletion Syndrome