Neonatal Levels of T-cell Receptor Excision Circles (TREC) in Patients with 22q11.2 Deletion Syndrome and Later Disease Features

[1] Botto LD(2003)A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population Pediatrics 112 101-7

[2] May K(1998)The annual incidence of DiGeorge/velocardiofacial syndrome J Med Genet 35 789-90

[3] Fernhoff PM(1993)Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis J Med Genet 30 813-7

[4] Correa A(2004)Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden Arch Dis Child 89 148-51

[5] Coleman K(1997)Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study J Med Genet 34 798-804

[6] Rasmussen SA(2004)Detection of 22q11.2 deletion among 139 patients with Di George/Velocardiofacial syndrome features In Vivo 18 603-8

[7] Devriendt K(2004)DiGeorge syndrome: an update Curr Opin Cardiol 19 201-4

[8] Fryns JP(1999)The DNA sequence of human chromosome 22 Nature 402 489-95

[9] Mortier G(1999)Chromosome 22q11 deletions in patients with selected outflow tract malformations Genet Couns 10 35-41

[10] van Thienen MN(2006)Tbx1 is regulated by forkhead proteins in the secondary heart field Dev Dyn 235 701-10

[1] Botto LD(2003)A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population Pediatrics 112 101-7

[2] May K(1998)The annual incidence of DiGeorge/velocardiofacial syndrome J Med Genet 35 789-90

[3] Fernhoff PM(1993)Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis J Med Genet 30 813-7

[4] Correa A(2004)Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden Arch Dis Child 89 148-51

[5] Coleman K(1997)Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study J Med Genet 34 798-804

[6] Rasmussen SA(2004)Detection of 22q11.2 deletion among 139 patients with Di George/Velocardiofacial syndrome features In Vivo 18 603-8

[7] Devriendt K(2004)DiGeorge syndrome: an update Curr Opin Cardiol 19 201-4

[8] Fryns JP(1999)The DNA sequence of human chromosome 22 Nature 402 489-95

[9] Mortier G(1999)Chromosome 22q11 deletions in patients with selected outflow tract malformations Genet Couns 10 35-41

[10] van Thienen MN(2006)Tbx1 is regulated by forkhead proteins in the secondary heart field Dev Dyn 235 701-10