Léri-Weill syndrome as part of a contiguous gene syndrome at Xp22.3. [electronic resource]
Producer: 19990707Description: 367-71 p. digitalISSN:- 0148-7299
- Abnormalities, Multiple -- genetics
- Adult
- Bone and Bones -- abnormalities
- Child, Preschool
- Chromosome Deletion
- Deafness -- genetics
- Female
- Forearm -- diagnostic imaging
- Homeodomain Proteins -- genetics
- Humans
- In Situ Hybridization, Fluorescence
- Male
- Mental Disorders -- genetics
- Radiography
- Seizures -- genetics
- Sex Chromosome Aberrations -- diagnosis
- Short Stature Homeobox Protein
- Syndrome
- X Chromosome
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Publication Type: Case Reports; Journal Article
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