DiGeorge (del22q11.2) syndrome is estimated to occur in 1:4,000 births, is the most common contiguous-gene deletion syndrome in humans, and is caused by autosomal dominant deletions in the 22q11.2 DiGeorge syndrome critical region (DGCR). Multiple microarray methods have been developed recently for
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Detection of female carriers of hunter's syndrome: Comparison of serum and hair-root analysis
โ Scribed by I. M. Archer; D. W. Rees; A. Oladimeji; F. S. Wusteman; P. S. Harper
- Publisher
- Springer
- Year
- 1982
- Tongue
- English
- Weight
- 236 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0141-8955
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