Individual haploinsufficient loci and the complex phenotype of DiGeorge syndrome
Author:
Publisher
Elsevier BV
Subject
Genetics,Molecular Medicine
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1. Molecular genetics of velo-cardio-facial syndrome;Velo-Cardio-Facial Syndrome;2005-06-30
2. Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome;Human Genetics;2005-03-19
3. Biased T-cell receptor repertoires in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome);Clinical and Experimental Immunology;2003-04-16
4. Molecular characterization of 22q11 deletion in a three-generation family with maternal transmission;American Journal of Medical Genetics;2002-03-07
5. A common cis-acting sequence in the DiGeorge critical region regulates bi-directional transcription of UFD1L and CDC45L;Mechanisms of Development;2001-10
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