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Selected Publication:

Schmidt, H; Uhrig, S; Lederer, G; Murken, J; Speicher, MR; Schuffenhauer, S.
Mosaicism for a dup(12)(q22q13) in a patient with hypomelanosis of Ito and asymmetry.
J Med Genet. 2000; 37(10):804-807 Doi: 10.1136/jmg.37.10.804 (- Case Report) [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Co-authors Med Uni Graz
Speicher Michael
Uhrig Sabine
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Find related publications in this database (using NLM MeSH Indexing)
Abnormalities, Multiple - genetics
Adult - genetics
Child - genetics
Child, Preschool - genetics
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Chromosome Breakage - genetics
Chromosome Deletion - genetics
Chromosomes, Artificial, Yeast - genetics
Chromosomes, Human, Pair 12 - genetics
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Fibroblasts - genetics
Gene Duplication - genetics
Genetic Heterogeneity - genetics
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Phenotype - genetics
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