Skip to search formSkip to main contentSkip to account menu

22q11

A chromosome band present on 22q
National Institutes of Health

Related topics

Related topics

3 relations
22qADRBK2 wt AlleleChromosomes

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
1999
1999
The deletions of 22q11--the Portuguese experience.
The patients with a chromosome 22q11 deletion have a variable phenotype which includes DiGeorge (DG) and Velocardiofacial (VCF… 
1998
1998
Relation of genotype 22 q 11 deletion to phenotype of pulmonary vessels in tetralogy of Fallot and pulmonary atresia – ventricular septal defect
Objective—To compare the morphology of the pulmonary vessels in tetralogy of Fallot or pulmonary atresia–ventricular septal… 
1996
1996
Heterotaxia syndromes and 22q11 deletion.
1 Binedell J, Soldan JR, Harper PS. Selection for presymptomatic testing for Huntington's disease: who decides? J Med Genet 1996… 
1996
1996
Progressive deficiencies in blood T cells associated with a 10p12-13 interstitial deletion.
We report on a 8-year-old patient affected by a selective T-cell defect associated with mental retardation and dysmorphic signs… 
1996
1996
Upper limb malformations in chromosome 22q11 deletions.
We read with interest the report of Cormier-Daire et al. in a recent issue of the journal, describing upper limb malformations in… 
1995
1995
Idiopathic hypoparathyroidism in two patients with 22q11 microdeletion.
The two patients were ascertained through their idiopathic hypoparathyroidism. The table shows their main clinical features and… 
1994
1994
Comparison of facial features of DiGeorge syndrome (DGS) due to deletion 10p13-10pter with DGS due to 22q11 deletion
DiGeorge syndrome (DGS) is a congenital anomaly consisting of cardiac defects, aplasia or hypoplasia of the thymus and parathroid… 
1987
1987
Cat-eye syndrome with different marker chromosomes in a mother and daughter.
Except for atypical eye findings in the daughter, a mother and daughter with bisatellited marker chromosomes had abnormalities… 
1984
1984
In situ hybridization and translocation breakpoint mapping. I. Nonidentical 22q11 breakpoints for the t(9;22) of CML and the t(8;22) of Burkitt lymphoma.
In situ chromosomal hybridization of a probe for part of the lambda light chain constant region (C lambda) has demonstrated that… 
Highly Cited
1983
Highly Cited
1983
Lambda Ig constant region genes are translocated to chromosome 8 in Burkitt's lymphoma with t(8;22).
By in situ hybridization of normal human chromosomes with a cloned genomic probe specific for the constant region of the lambda…