A new 3p interstitial deletion including the entire MITE gene causes a variation of tietz/waardenburg type IIA syndromes
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| Veröffentlicht in: | American journal of medical genetics. Part A 2007, Vol.143 (6), p.619-624 |
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| container_end_page | 624 |
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| container_issue | 6 |
| container_start_page | 619 |
| container_title | American journal of medical genetics. Part A |
| container_volume | 143 |
| creator | SCHWARZBRAUN, Thomas OFNER, Lisa GILLESSEN-KAESBACH, Gabriele SCHAPERDOTH, Barbara PREISEGGER, Karl-Heinz WINDPASSINGER, Christian WAGNER, Klaus PETEK, Erwin KROISEL, Peter M |
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| fulltext | fulltext |
| identifier | ISSN: 1552-4825 |
| ispartof | American journal of medical genetics. Part A, 2007, Vol.143 (6), p.619-624 |
| issn | 1552-4825 1552-4833 |
| language | eng |
| recordid | cdi_pascalfrancis_primary_18611195 |
| source | Wiley Online Library Journals Frontfile Complete |
| subjects | Biological and medical sciences Classical genetics, quantitative genetics, hybrids Dermatology Fundamental and applied biological sciences. Psychology Genetics of eukaryotes. Biological and molecular evolution Human Medical genetics Medical sciences Pigmentary diseases of the skin |
| title | A new 3p interstitial deletion including the entire MITE gene causes a variation of tietz/waardenburg type IIA syndromes |
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