Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Gewählte Publikation:
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
FullText
FullText_MUG
- Co-Autor*innen der Med Uni Graz
- Speicher Michael
- Uhrig Sabine
- Altmetrics:
- Dimensions Citations:
- Plum Analytics:
- Scite (citation analytics):
- Find related publications in this database (using NLM MeSH Indexing)
- Abnormalities, Multiple - genetics
- Adult - genetics
- Child - genetics
- Child, Preschool - genetics
- Chromosome Banding - genetics
- Chromosome Breakage - genetics
- Chromosome Deletion - genetics
- Chromosomes, Artificial, Yeast - genetics
- Chromosomes, Human, Pair 12 - genetics
- Chromosomes, Human, Pair 7 - genetics
- Female - genetics
- Fibroblasts - genetics
- Gene Duplication - genetics
- Genetic Heterogeneity - genetics
- Genotype - genetics
- Humans - genetics
- Hypopigmentation - genetics
- In Situ Hybridization, Fluorescence - genetics
- Infant - genetics
- Infant, Newborn - genetics
- Karyotyping - genetics
- Lymphocytes - genetics
- Male - genetics
- Mental Retardation - genetics
- Mosaicism - genetics
- Phenotype - genetics
- Trisomy - genetics