Related content

Homozygous deletion of the UGT2B17 gene is not associated with osteoporosis risk in elderly Caucasian women

By Chew S.   Mullin B.   Lewis J.   Spector T.   Prince R.   Wilson S.  

Osteoporosis International, Vol. 22, Iss. 6, 2011-06 ,pp. : 1981-1986

Springer Publishing Company

Access to resources Recommend Favorite

Polymorphisms in the 5′ flank of COL1A1 gene and osteoporosis: meta-analysis of published studies

By Jin H.   Evangelou E.   Ioannidis J.   Ralston S.  

Osteoporosis International, Vol. 22, Iss. 3, 2011-03 ,pp. : 911-921

Springer Publishing Company

Access to resources Recommend Favorite

Identification of a novel STAT3 mutation in a patient with hyper-IgE syndrome

By Mogensen Trine H.   Jakobsen Marianne A.   Larsen Carsten S.  

Scandinavian Journal of Infectious Diseases, Vol. 45, Iss. 3, 2013-03 ,pp. : 235-238

Informa Healthcare

Access to resources Recommend Favorite

Erratum to: A novel long-QT 5 gene mutation in the C-terminus (V109I) is associated with a mild phenotype

By Schulze-Bahr Eric   Schwarz Martin   Hauenschild Susan   Wedekind Horst   Funke Harald   Haverkamp Wilhelm   Breithardt Günter   Pongs Olaf   Isbrandt Dirk  

Journal of Molecular Medicine, Vol. 79, Iss. 9, 2001-09 ,pp. : 547-547

Springer Publishing Company

Access to resources Recommend Favorite

A novel long-QT 5 gene mutation in the C-terminus (V109I) is associated with a mild phenotype

By Schulze-Bahr Eric   Schwarz Martin   Hoffmann Susanne   Wedekind Horst   Funke Harald   Haverkamp Wilhelm   Breithardt Günter   Pongs Olaf   Isbrandt Dirk  

Journal of Molecular Medicine, Vol. 79, Iss. 9, 2001-09 ,pp. : 504-509

Springer Publishing Company

Access to resources Recommend Favorite