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SHR Neuro Krebs Kardio Lipid Stoffw Microb

Schwarzbraun, T; Ofner, L; Gillessen-Kaesbach, G; Schaperdoth, B; Preisegger, KH; Windpassinger, C; Wagner, K; Petek, E; Kroisel, PM.
A new 3p interstitial deletion including the entire MITF gene causes a variation of Tietz/Waardenburg type IIA syndromes.
Am J Med Genet A. 2007; 143(6): 619-624. Doi: 10.1002/ajmg.a.31627 (- Case Report)
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Führende Autor*innen der Med Uni Graz
Kroisel Peter
Schwarzbraun Thomas
Co-Autor*innen der Med Uni Graz
Ofner-Ziegenfuss Lisa
Petek Erwin
Wagner Klaus
Windpassinger Christian
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Find related publications in this database (using NLM MeSH Indexing)
Abnormalities, Multiple - genetics
Chromosome Banding - genetics
Chromosome Deletion - genetics
Chromosome Mapping - genetics
Chromosomes, Human, Pair 3 - genetics
Gene Deletion - genetics
Genetic Predisposition to Disease - genetics
Humans - genetics
Infant - genetics
Karyotyping - genetics
Male - genetics
Microphthalmia-Associated Transcription Factor - genetics
Microsatellite Repeats - genetics
Pedigree - genetics
Pigmentation Disorders - classification
Waardenburg's Syndrome - classification

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