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Deletions within chromosome 22q11 in familial congenital heart disease

โœ Scribed by Wilson, D.I; Goodship, J.A; Burn, J; Cross, I.E; Scambler, P.J


Book ID
123125535
Publisher
The Lancet
Year
1992
Tongue
English
Weight
407 KB
Volume
340
Category
Article
ISSN
0140-6736

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Familial deletions of chromosome 22q11
โœ Digilio, Maria Cristina; Marino, Bruno; Giannotti, Aldo; Dallapiccola, Bruno ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 7 KB ๐Ÿ‘ 2 views

We read with interest the paper by Leana-Cox et al. [1996] which reported on 5 families with recurrent Di-George/velocardiofacial syndrome and deletions of chromosome 22q11 (del22q11), and which reviewed the pertinent literature. The authors observed that up to 25% of del22q11 are inherited. Particu