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Autosomal recessive truncating MAB21L1 mutation associated with a syndromic scrotal agenesis

Document Type

Article

Author

Bruel, A.-L.; Masurel-Paulet, A.; Rivière, J.-B.; Duffourd, Y.; Lehalle, D.; Kuentz, P.; Thauvin-Robinet, C.; Faivre, L.; Thevenon, J.; Bensignor, C.; Huet, F.; Borgnon, J.; Roucher, F.; Deleuze, J.-F.

Source

In: Clinical Genetics. (Clinical Genetics, 1 February 2017, 91(2):333-338)

Subject

Language

English

ISSN

13990004
00099163

Online Access

Full Text (Wiley Journals) Full Text (Wiley-DB) Web of Science JCR 저널정보 Scopus Find it@PNU

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