Weill-Marchesani syndrome--possible linkage of the autosomal dominant form to 15q21.1. [electronic resource]
Producer: 19970207Description: 68-75 p. digitalISSN:- 0148-7299
- Abnormalities, Multiple -- genetics
- Adolescent
- Adult
- Child
- Child, Preschool
- Chromosomes, Human, Pair 15
- Dwarfism -- genetics
- Eye Abnormalities -- genetics
- Female
- Fibrillin-1
- Fibrillins
- Genes, Dominant
- Genetic Linkage
- Humans
- Immunologic Techniques
- Infant
- Male
- Microfilament Proteins -- genetics
- Microsatellite Repeats
- Middle Aged
- Pedigree
- Syndrome
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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