Is SHORT syndrome another phenotypic variation of PITX2? [electronic resource]
Producer: 20050302Description: 406-9 p. digitalISSN:- 1552-4825
- Adult
- Chromosomes, Human, Pair 1 -- genetics
- Chromosomes, Human, Pair 4 -- genetics
- Eye Abnormalities -- genetics
- Female
- Homeodomain Proteins -- genetics
- Humans
- Infant
- Male
- Phenotype
- Polycystic Ovary Syndrome -- genetics
- Syndrome
- Transcription Factors -- genetics
- Translocation, Genetic -- genetics
- Homeobox Protein PITX2
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Publication Type: Case Reports; Journal Article
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