Concepedia

Frequency of 22q11.2 microdeletion in sporadic non-syndromic tetralogy of Fallot cases

Luciana Gioli‐Pereira, Anabela Pereira, D. Bergara, Sonia M Mesquita, Antônio Augusto Lopes, José Eduardo Krieger

International Journal of Cardiology · 2007 · 25 citations · 26 references

DOI

Concepts

References

26

A simple salting out procedure for extracting DNA from human nucleated cells

S.A. Miller, Dale D. Dykes, Herbert F. Polesky · Nucleic Acids Research · 1988 · 20.6K citations · Full text

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Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

A K Ryan, Judith A. Goodship, David I. Wilson et al. · Journal of Medical Genetics · 1997 · 1.2K citations · Full text

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DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

Loydie A. Jerome, Virginia E. Papaioannou · Nature Genetics · 2001 · 1.1K citations

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Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice

Elizabeth A. Lindsay, Francesca Vitelli, Hong Hua Su et al. · Nature · 2001 · 1K citations

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TBX1 Is Responsible for Cardiovascular Defects in Velo-Cardio-Facial/DiGeorge Syndrome

Sandra Merscher, Birgit Funke, Jonathan A. Epstein et al. · Cell · 2001 · 988 citations

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