Holoprosencephaly with cerebellar vermis hypoplasia in 13q deletion syndrome: Critical region for cerebellar dysgenesis within 13q32.2q34. [electronic resource]
Producer: 20160310Description: 714-8 p. digitalISSN:- 1872-7131
- Brain -- pathology
- Chromosome Deletion
- Chromosome Disorders -- complications
- Chromosomes, Human, Pair 13 -- genetics
- DNA-Binding Proteins
- Dandy-Walker Syndrome -- complications
- Female
- Gene Deletion
- Holoprosencephaly -- complications
- Humans
- Infant
- Magnetic Resonance Imaging
- Male
- Nuclear Proteins -- genetics
- Transcription Factors -- genetics
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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