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A 2-Mb critical region implicated in the microcephaly associated with terminal 1q deletion syndrome

✍ Scribed by Anthony D. Hill; Bernard S. Chang; R. Sean Hill; Levi A. Garraway; Adria Bodell; William R. Sellers; Christopher A. Walsh


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
223 KB
Volume
143A
Category
Article
ISSN
1552-4825

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Patient with a 22q11.2 deletion with no
✍ McQuade, Leon; Christodoulou, John; Budarf, Marcia; Sachdev, Rani; Wilson, Mered πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 39 KB πŸ‘ 3 views

The apparent lack of genotype/phenotype correlation in patients with the DiGeorge anomaly and velocardiofacial syndrome (DGA/VCFS; the "22q11 deletion syndrome") indicates a complex genetic condition. Most cases, whatever the phenotype, have a 1.5-3 ## Mb chromosomal deletion that includes the mini