Carbohydrate-deficient glycoprotein syndrome: hidden treasures. 1997

W A Gahl

UI MeSH Term Description Entries
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D018981 Congenital Disorders of Glycosylation A genetically heterogeneous group of heritable disorders resulting from defects in protein N-glycosylation. Carbohydrate-Deficient Glycoprotein Syndrome,Glycoprotein Syndrome, Carbohydrate-Deficient,Carbohydrate Deficient Glycoprotein Syndrome,Carbohydrate-Deficient Glycoprotein Syndromes,Syndrome, Carbohydrate-Deficient Glycoprotein,Syndromes, Carbohydrate-Deficient Glycoprotein

Related Publications

W A Gahl
December 1995, Nihon rinsho. Japanese journal of clinical medicine,
W A Gahl
January 1996, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie,
W A Gahl
November 1994, Ugeskrift for laeger,
W A Gahl
February 2000, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie,
W A Gahl
April 1991, Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke,
W A Gahl
January 1998, Ryoikibetsu shokogun shirizu,
W A Gahl
April 1999, Journal of inherited metabolic disease,
W A Gahl
September 2004, Journal of the Formosan Medical Association = Taiwan yi zhi,
W A Gahl
January 1993, Journal of inherited metabolic disease,
W A Gahl
August 2001, Indian pediatrics,
Copied contents to your clipboard!