Submicroscopic deletion in chromosome 22q11 in trizygous triplet siblings and their father Clinical variability of 22q11 deletion

Author:

Devriendt K.,Hoestenberghe R. Van,Hole C. Van,Devlieger H.,Gewillig M.,Moerman Ph.,Berghe H.,Fryns J. P.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference20 articles.

1. Detection of amplified VNTR alleles by direct chemiluminescence: application to the genetic identification of biological samples in forensic cases;Decorte;Experientia,1991

2. Third and fourth pouch/arch syndrome (DiGeorge anomaly) in one dizygote twin;Martino;Eur J Pediatr,1995

3. Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial cases;Desmaze;Am J Hum Genet,1993

4. A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11;Driscoll;Am J Hum Genet,1992

5. Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis;Driscoll;J Med Genet,1993

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