A Feingold syndrome case with previously undescribed features and a new mutation. [electronic resource]
Producer: 20091116Description: 261-7 p. digitalISSN:- 1015-8146
- Abnormalities, Multiple -- diagnosis
- Chromosome Aberrations
- Craniofacial Abnormalities -- diagnosis
- Duodenum -- abnormalities
- Esophageal Atresia -- diagnosis
- Fingers -- abnormalities
- Genes, Dominant -- genetics
- Humans
- Infant
- Intestinal Atresia -- diagnosis
- Male
- Microcephaly -- diagnosis
- Mutation, Missense -- genetics
- N-Myc Proto-Oncogene Protein
- Nuclear Proteins -- genetics
- Oncogene Proteins -- genetics
- Phenotype
- Spasms, Infantile -- diagnosis
- Syndrome
- Turkey
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Publication Type: Case Reports; Journal Article
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