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PHGDH-related microcephalic dwarfism in two fetuses: Expanding the phenotypical spectrum of L-serine biosynthesis defect

Document Type

Article

Author

Cuinat, S.; Edery, P.; Chatron, N.; Lesca, G.; Putoux, A.; Quélin, C.; Pasquier, L.; Odent, S.; Loget, P.; Aussel, D.; Laquerrière, A.; Proisy, M.; Mazoyer, S.; Delous, M.

Source

In: European Journal of Medical Genetics. (European Journal of Medical Genetics, November 2023, 66(11))

Subject

Language

English

ISSN

18780849
17697212

Online Access

Full Text (ScienceDirect 종량제) Full Text (Clinical Key) Web of Science JCR 저널정보 Scopus Find it@PNU

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