Costello syndrome with severe cutis laxa and mosaic HRAS G12S mutation. [electronic resource]
Producer: 20110204Description: 2861-4 p. digitalISSN:- 1552-4833
- Amino Acid Sequence
- Amino Acid Substitution -- genetics
- Base Sequence
- Costello Syndrome -- complications
- Cutis Laxa -- complications
- DNA Mutational Analysis
- Female
- Humans
- Infant
- Infant, Newborn
- Male
- Molecular Sequence Data
- Mosaicism
- Mutation -- genetics
- Pregnancy
- Proto-Oncogene Proteins p21(ras) -- chemistry
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Publication Type: Case Reports; Journal Article
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