Clinical variability in patients with Apert's syndrome. [electronic resource]
Producer: 19990401Description: 443-7 p. digitalISSN:- 0022-3085
- Acrocephalosyndactylia -- diagnosis
- Base Sequence -- genetics
- Brain -- pathology
- Female
- Fetus -- anatomy & histology
- Humans
- Infant, Newborn
- Magnetic Resonance Imaging
- Male
- Mutation -- genetics
- Phenotype
- Radiography
- Receptor Protein-Tyrosine Kinases -- genetics
- Receptor, Fibroblast Growth Factor, Type 2
- Receptors, Fibroblast Growth Factor -- genetics
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Publication Type: Journal Article
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