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1 Ergebnisse
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SH2D1A mutation analysis for diagnosis of XLP in typical an..:
Yin, L.
;
Ferrand, V.
;
Lavoué, M.-F.
...
Human Genetics. 105 (1999) 5 - p. 501-505 , 1999
Link:
https://doi.org/10.1007/s004399900168
RT Journal T1
SH2D1A mutation analysis for diagnosis of XLP in typical and atypical patients
UL https://suche.suub.uni-bremen.de/peid=cr-10.1007_s004399900168&Exemplar=1&LAN=DE A1 Yin, L. A1 Ferrand, V. A1 Lavoué, M.-F. A1 Hayoz, D. A1 Philippe, N. A1 Souillet, G. A1 Seri, M. A1 Giacchino, R. A1 Castagnola, E. A1 Hodgson, S. A1 Sylla, B.S. A1 Romeo, G. PB Springer Science and Business Media LLC YR 1999 SN 0340-6717 SN 1432-1203 JF Human Genetics VO 105 IS 5 SP 501 OP 505 LK http://dx.doi.org/https://doi.org/10.1007/s004399900168 DO https://doi.org/10.1007/s004399900168 SF ELIB - SuUB Bremen
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