Apparently unrelated cytogenetic abnormalities among 462 probands referred for the detection of del(22q) by FISH
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference29 articles.
1. Is the genetic basis of DiGeorge syndrome in HAND?
2. Disease associated balanced chromosome rearrangements: a resource for large scale genotype-phenotype delineation in man
3. A deletion in chromosome 22 can cause digeorge syndrome
4. The fragile X syndrome.
5. Submicroscopic deletion in chromosome 22q11 in trizygous triplet siblings and their father Clinical variability of 22q11 deletion
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1. 22q11.2 Deletion Syndrome: Laboratory Diagnosis and TBX1 and FGF8 Mutation Screening;Journal of Pediatric Genetics;2015-07-17
2. Genetics of Chromosome 22q11.2 Deletion Syndrome;eLS;2013-01-15
3. BAC array CGH in patients with Velocardiofacial syndrome-like features reveals genomic aberrations on chromosome region 1q21.1;BMC Medical Genetics;2009-12
4. Síndrome de deleção 22q11.2: importância da avaliação clínica e técnica de FISH;Revista da Associação Médica Brasileira;2009
5. Unrelated chromosomal anomalies found in patients with suspected 22q11.2 deletion;American Journal of Medical Genetics Part A;2008
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