Industrial Microbiology (MeSH) < Infant (MeSH) < Infant Formula (chemistry)

Facettes : Author.f AffPays.f AffRegion.f AffVille.f AffOrg.f Mesh.f MeshFr.f KwdFr.f

List of bibliographic references indexed by Infant (MeSH)

Number of relevant bibliographic references: 5.

Ident.	Authors (with country if any)	Title
000438 (2016)	Chiao-Fan Chiu [Taïwan] ; Ju-Li Lin [Taïwan] ; Jainn-Jim Lin [Taïwan] ; Min-Hua Tseng [Taïwan] ; Fu-Sung Lo [Taïwan] ; Ming-Chou Chiang [Taïwan]	Nonketotic Hyperglycinemia of Infants in Taiwan.
000586 (2014)	Peter R. Baker [États-Unis] ; Marisa W. Friederich ; Michael A. Swanson ; Tamim Shaikh ; Kaustuv Bhattacharya ; Gunter H. Scharer ; Joseph Aicher ; Geralyn Creadon-Swindell ; Elizabeth Geiger ; Kenneth N. Maclean ; Wang-Tso Lee ; Charu Deshpande ; Mary-Louise Freckmann ; Ling-Yu Shih ; Melissa Wasserstein ; Malene B. Rasmussen ; Allan M. Lund ; Peter Procopis ; Jessie M. Cameron ; Brian H. Robinson ; Garry K. Brown ; Ruth M. Brown ; Alison G. Compton ; Carol L. Dieckmann ; Renata Collard ; Curtis R. Coughlin ; Elaine Spector ; Michael F. Wempe ; Johan L K. Van Hove	Variant non ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5.
000710 (2013)	Xiaohui Dong [République populaire de Chine] ; Qingping Wu ; Jumei Zhang ; Shuping Mo ; Xiaoxia Kou ; Weipeng Guo	Sequencing of the grxB gene of Cronobacter spp. and the development of a PCR assay for its identification.
000777 (2013)	Rie Ohba [Japon] ; Kazumichi Furuyama ; Kenichi Yoshida ; Tohru Fujiwara ; Noriko Fukuhara ; Yasushi Onishi ; Atsushi Manabe ; Etsuro Ito ; Keiya Ozawa ; Seiji Kojima ; Seishi Ogawa ; Hideo Harigae	Clinical and genetic characteristics of congenital sideroblastic anemia: comparison with myelodysplastic syndrome with ring sideroblast (MDS-RS).
000988 (2010)	Anke K. Bergmann [États-Unis] ; Dean R. Campagna ; Erin M. Mcloughlin ; Suneet Agarwal ; Mark D. Fleming ; Sylvia S. Bottomley ; Ellis J. Neufeld	Systematic molecular genetic analysis of congenital sideroblastic anemia: evidence for genetic heterogeneity and identification of novel mutations.

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