Localisation of the gene responsible for fechtner syndrome in a region <600 Kb on 22q11-q13. [electronic resource]
Producer: 20001207Description: 895-9 p. digitalISSN:- 1018-4813
- Abnormalities, Multiple -- genetics
- Adult
- Child
- Chromosome Mapping
- Chromosomes, Human, Pair 22 -- genetics
- DNA -- genetics
- Eye Abnormalities
- Family Health
- Female
- Genotype
- Haplotypes
- Hearing Loss, Sensorineural
- Humans
- Italy
- Male
- Microsatellite Repeats
- Middle Aged
- Nephritis
- Pedigree
- Syndrome
- Thrombocytopenia
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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