Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37). [electronic resource]
Producer: 19890630Description: 350-2 p. digitalISSN:- 0148-7299
- Abnormalities, Multiple -- genetics
- Chromosome Aberrations -- pathology
- Chromosome Banding
- Chromosome Deletion
- Chromosome Disorders
- Chromosomes, Human, Pair 2
- Facial Muscles -- physiopathology
- Growth Disorders -- genetics
- Humans
- Infant
- Intellectual Disability -- genetics
- Karyotyping
- Male
- Muscle Hypotonia -- genetics
- Phenotype
No physical items for this record
Publication Type: Case Reports; Journal Article; Research Support, U.S. Gov't, P.H.S.
There are no comments on this title.
Log in to your account to post a comment.