A new case with 10q23 interstitial deletion encompassing both PTEN and BMPR1A narrows the genetic region deleted in juvenile polyposis syndrome. [electronic resource]
Producer: 20131114Description: 43-7 p. digitalISSN:- 2190-3883
- Bone Morphogenetic Protein Receptors, Type I -- genetics
- Child, Preschool
- Chromosomes, Human, Pair 10 -- genetics
- Developmental Disabilities -- genetics
- Genotype
- Hamartoma Syndrome, Multiple -- genetics
- Humans
- Intestinal Polyposis -- congenital
- Male
- Neoplastic Syndromes, Hereditary -- genetics
- PTEN Phosphohydrolase -- genetics
- Sequence Deletion
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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