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Titolo:
Congenital disorders of glycosylation IIa cause growth retardation, mentalretardation, and facial dysmorphism
Autore:
Cormier-Daire, V; Amiel, J; Vuillaumier-Barrot, S; Tan, J; Durand, G; Munnich, A; Le Merrer, M; Seta, N;
Indirizzi:
Hop Necker Enfants Malad, Dept Genet, F-75743 Paris 15, France Hop Necker Enfants Malad Paris France 15 Genet, F-75743 Paris 15, France Hop Necker Enfants Malad, INSERM, U393, F-75743 Paris, France Hop Necker Enfants Malad Paris France F-75743 393, F-75743 Paris, France Hosp Sick Children, Dept Biochem, Toronto, ON M5G 1X8, Canada Hosp Sick Children Toronto ON Canada M5G 1X8 Toronto, ON M5G 1X8, Canada Hop Bichat Claude Bernard, Dept Biochem, F-75877 Paris 18, France Hop Bichat Claude Bernard Paris France 18 chem, F-75877 Paris 18, France Fac Pharm, Lab Hyg & Sante Publ, Paris, France Fac Pharm Paris FranceFac Pharm, Lab Hyg & Sante Publ, Paris, France
Titolo Testata:
JOURNAL OF MEDICAL GENETICS
fascicolo: 11, volume: 37, anno: 2000,
pagine: 875 - 877
SICI:
0022-2593(200011)37:11<875:CDOGIC>2.0.ZU;2-W
Fonte:
ISI
Lingua:
ENG
Soggetto:
DEFICIENT GLYCOPROTEIN-SYNDROME; SYNDROME TYPE-I;
Tipo documento:
Letter
Natura:
Periodico
Settore Disciplinare:
Clinical Medicine
Life Sciences
Citazioni:
13
Recensione:
Indirizzi per estratti:
Indirizzo: Cormier-Daire, V Hop Necker Enfants Malad, Dept Genet, 149 Rue Sevres, F-75743 Paris 15, France Hop Necker Enfants Malad 149 Rue Sevres Paris France15
Citazione:
V. Cormier-Daire et al., "Congenital disorders of glycosylation IIa cause growth retardation, mentalretardation, and facial dysmorphism", J MED GENET, 37(11), 2000, pp. 875-877


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 30/11/20 alle ore 19:44:04