A patient with Baller-Gerold syndrome and midline NK/T lymphoma. [electronic resource]
Producer: 20090617Description: 755-9 p. digitalISSN:- 1552-4833
- Alleles
- Base Sequence
- Child
- Codon, Nonsense
- Craniosynostoses -- genetics
- DNA Mutational Analysis
- DNA, Complementary -- genetics
- Female
- Frameshift Mutation
- Genes, Recessive
- Humans
- Limb Deformities, Congenital -- genetics
- Lymphoma, T-Cell -- genetics
- Molecular Sequence Data
- Nuclear Proteins -- genetics
- Phenotype
- RecQ Helicases -- genetics
- Rothmund-Thomson Syndrome -- genetics
- Sequence Deletion
- Syndrome
- Twist-Related Protein 1 -- genetics
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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