Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay
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概要
- 論文の詳細を見る
- Springer Japanの論文
- 2007-01-01
著者
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Antonucci Ivana
Department Of Biomedical Sciences And Aging Research Center Ce.s.i. G. D'annunzio University Fo
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Fischetto Rita
Azienda Ospedaliera "di Venere" E "giovanni Xxiii" Sezione Di Genetica Medica
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Calabrese Giuseppe
Department Of Biomedical Sciences And Aging Research Center Ce.s.i. G. D'annunzio University Fo
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GATTA Valentina
Department of Biomedical Sciences and Aging Research Center, Ce.S.I., G. d'Annunzio University Found
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MORIZIO Elisena
Service of Human Genetics, Pescara Hospital
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PALKA Chiara
IRCCS-CSS San Giovanni Rotondo and CSS-Mendel Rome
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MOKINI Vahe
Service of Medical Genetics, University Hospital Center "Mother Theresa"
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TUMINI Stefano
Dipartimento di Pediatria e Ginecologia, Universita "G D'Annunzio"
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STUPPIA Liborio
Department of Biomedical Sciences and Aging Research Center, Ce.S.I., G. d'Annunzio University Found
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Mokini Vahe
Service Of Medical Genetics University Hospital Center "mother Theresa
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Tumini Stefano
Dipartimento Di Pediatria E Ginecologia Universita "g D'annunzio
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Stuppia Liborio
Department Of Biomedical Sciences And Aging Research Center Ce.s.i. G. D'annunzio University Fo
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Gatta Valentina
Department Of Biomedical Sciences And Aging Research Center Ce.s.i. G. D'annunzio University Fo
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Morizio Elisena
Service Of Human Genetics Pescara Hospital
関連論文
- Audiogenic Seizures Susceptibility in Transgenic Mice with Fragile X Syndrome
- Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay