Author:
Lafabregue E.,Chaby G.,Vabres P.,Carmi E.
Reference17 articles.
1. Case Report: Interstitial Deletion 21q22.13-Q22.3 in a Male Patient with Developmental Delay, Holoprosencephaly, Dysmorphic Features, and Multiple Congenital Anomalies;Hussein;J Mol Biomark Diagn,2015
2. Genotype–phenotype correlations in Down syndrome identified array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21;Lyle;Eur J Hum Genet,2009
3. Distinctive phenotypic abnormalities associated with submicroscopic 21q22 deletion including DYRK1A;Oegema;Mol Syndromol,2010
4. Genomic analysis of partial 21q monosomies with variable phenotypes;Roberson;Eur J Hum Genet,2011
5. Frontonasal dysplasia, callosal agenesis, basal encephalocele, and eye anomalies syndrome with a partial 21q22.3 deletion;Guion-Almeida;Am J Med Genet,2012
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