Novel clinical features in a child with partial deletion of chromosome 11 [del(11)(q24.2)]: Further evidence for phenotypic heterogeneity
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference5 articles.
1. Genomewide Linkage Analysis of Body Mass Index across 28 Years of the Framingham Heart Study
2. The 11q terminal deletion disorder: A prospective study of 110 cases
3. An (11;21) Translocation in Four Generations with Chromosome 11 Abnormalities in the Offspring
4. DFNB20: a novel locus for autosomal recessive, non-syndromal sensorineural hearing loss maps to chromosome 11q25–qter
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1. First Report of Jacobsen Syndrome with Dextrocardia Diagnosed with del(11)(q24q25);Molecular Syndromology;2022
2. Genomic microarray technologies for the cytogenetics laboratory;The AGT Cytogenetics Laboratory Manual;2017-03-04
3. Mice Haploinsufficient for Ets1 and Fli1 Display Middle Ear Abnormalities and Model Aspects of Jacobsen Syndrome;The American Journal of Pathology;2015-07
4. Subtelomeric monosomy 11q and trisomy 16q in siblings and an unrelated child: Molecular characterization of two der(11)t(11;16);American Journal of Medical Genetics Part A;2011-08-10
5. Paris-Trousseau-type macrothrombocytopenia without 11q deletion;Pediatrics International;2010-04
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