MEHMO, a novel syndrome: assignment of disease locus to Xp21.1–p22.13
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| Veröffentlicht in: | European journal of human genetics : EJHG 1999-09, Vol.7 (6), p.621-622 |
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| Sprache: | eng |
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| container_end_page | 622 |
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| container_issue | 6 |
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| container_title | European journal of human genetics : EJHG |
| container_volume | 7 |
| creator | DeLozier-Blanchet, Célia D Haenggeli, Charles-Antoine Bottani, Armand |
| description | |
| doi_str_mv | 10.1038/sj.ejhg.5200364 |
| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 1018-4813 |
| ispartof | European journal of human genetics : EJHG, 1999-09, Vol.7 (6), p.621-622 |
| issn | 1018-4813 1476-5438 |
| language | eng |
| recordid | cdi_crossref_primary_10_1038_sj_ejhg_5200364 |
| source | SpringerLink (Online service); EZB Electronic Journals Library |
| title | MEHMO, a novel syndrome: assignment of disease locus to Xp21.1–p22.13 |
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