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p63 mutations account for a range of congenital anomaly syndromes with a clear genotype phenotype correlation

Document Type

Journal

Author

Brunner, H; McGrath, JA; Celli, J; Duijf, P; Gurrieri, F; McKeon, F; Propping, P; Bamshad, M; van Bokhoven, H; Hamel, B; Neri, G; Doetsch, V; de Waal, R; Yang, A; Vanmolkot, K

Source

JOURNAL OF MEDICAL GENETICS; SEP 2000, 37 pS27-pS27, 1p. Supplement: 1

Subject

Language

English

ISSN

00222593

Online Access

Full Text (BMJ Journals) Full Text (ProQuest Central) Web of Science JCR 저널정보 Find it@PNU

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