Prenatal manifestation in a family affected by nevoid basal cell carcinoma syndrome. [electronic resource]
Producer: 20081113Description: 472-8 p. digitalISSN:- 1769-7212
- Basal Cell Nevus Syndrome -- diagnosis
- Corpus Callosum -- pathology
- Craniofacial Abnormalities -- diagnosis
- Exons
- Family Health
- Female
- Gene Deletion
- Humans
- Mutation
- Patched Receptors
- Patched-1 Receptor
- Pedigree
- Pregnancy
- Prenatal Diagnosis
- Receptor, Melanocortin, Type 1 -- genetics
- Receptors, Cell Surface -- genetics
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Publication Type: Case Reports; Journal Article
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