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1 Ergebnisse
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A novel heterozygous MAP2K1 mutation in a patient with Noon..:
Nishi, Eriko
;
Mizuno, Seiji
;
Nanjo, Yuka
...
American Journal of Medical Genetics Part A. 167 (2014) 2 - p. 407-411 , 2014
Link:
https://doi.org/10.1002/ajmg.a.36842
RT Journal T1
A novel heterozygous MAP2K1 mutation in a patient with Noonan syndrome with multiple lentigines
UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_ajmg.a.36842&Exemplar=1&LAN=DE A1 Nishi, Eriko A1 Mizuno, Seiji A1 Nanjo, Yuka A1 Niihori, Tetsuya A1 Fukushima, Yoshimitsu A1 Matsubara, Yoichi A1 Aoki, Yoko A1 Kosho, Tomoki PB Wiley YR 2014 SN 1552-4825 SN 1552-4833 JF American Journal of Medical Genetics Part A VO 167 IS 2 SP 407 OP 411 LK http://dx.doi.org/https://doi.org/10.1002/ajmg.a.36842 DO https://doi.org/10.1002/ajmg.a.36842 SF ELIB - SuUB Bremen
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