De novo inv(2)(p12q34) associated with Klippel-Feil anomaly and hypodontia. [electronic resource]
Producer: 20040220Description: 594-7 p. digitalISSN:- 0340-6199
- Abnormalities, Multiple -- diagnosis
- Adolescent
- Anodontia -- diagnosis
- Chromosome Inversion
- Chromosomes, Human, Pair 2 -- genetics
- Congenital Hypothyroidism
- Facial Asymmetry -- congenital
- Female
- Hearing Loss -- congenital
- Humans
- Hypothyroidism -- diagnosis
- Klippel-Feil Syndrome -- diagnosis
- Psychomotor Disorders -- congenital
- Radiography
- Scoliosis -- congenital
- Speech Disorders -- diagnosis
- Spine -- diagnostic imaging
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Publication Type: Case Reports; Journal Article
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