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B Haglund

Showing results (51-60 of 79) with videos related to

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Family Planning Perspectives|May 2, 2001
Teenage childbearing and long-term socioeconomic consequences: a case study in SwedenP O Olausson, B Haglund, G R Weitoft, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|June 22, 2013
Increased risk of severe maternal morbidity (near-miss) among immigrant women in Sweden: a population register-based studyA Wahlberg, M Rööst, B Haglund, et al.
Acta Paediatrica Japonica : Overseas Edition|January 1, 1988
Clinical forms of congenital adrenal hyperplasia: restriction length polypmorphism patterns in the CYP21 geneE M Ritzén, B Haglund-Stengler, W Dorobek, et al.
Obstetrics and Gynecology|May 8, 1998
Routine ultrasound screening in pregnancy and the children's subsequent neurologic developmentH Kieler, G Ahlsten, B Haglund, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|January 31, 2007
Being born small for gestational age increases the risk of severe pre-eclampsiaK Zetterström, S Lindeberg, B Haglund, et al.
The American Journal of Psychiatry|January 1, 1977
Hydroxyzine in the treatment of alcohol withdrawalS L Dilts, D L Keleher, G Hoge, et al.
International Journal of Obesity (2005)|January 23, 2008
Higher education and more physical activity limit the development of obesity in a Swedish rural population. The Skaraborg ProjectM Nyholm, B Gullberg, B Haglund, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1991
Haplotypes of the steroid 21-hydroxylase gene region encoding mild steroid 21-hydroxylase deficiencyB Haglund-Stengler, E Martin Ritzén, J Gustafsson, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1992
Steroid 21-hydroxylase deficiency: three additional mutated alleles and establishment of phenotype-genotype relationships of common mutationsA Wedell, E M Ritzén, B Haglund-Stengler, et al.
Human Genetics|October 1, 1990
TaqI HLA-B and -DRB RFLP analysis can predict disease in siblings of affected children with 21-hydroxylase deficiencyO Olerup, H Luthman, E M Ritzén, et al.
Pageof 8

Showing results (51-60 of 79) with videos related to

Sort By:
Pageof 8
Family Planning Perspectives|May 2, 2001
Teenage childbearing and long-term socioeconomic consequences: a case study in SwedenP O Olausson, B Haglund, G R Weitoft, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|June 22, 2013
Increased risk of severe maternal morbidity (near-miss) among immigrant women in Sweden: a population register-based studyA Wahlberg, M Rööst, B Haglund, et al.
Acta Paediatrica Japonica : Overseas Edition|January 1, 1988
Clinical forms of congenital adrenal hyperplasia: restriction length polypmorphism patterns in the CYP21 geneE M Ritzén, B Haglund-Stengler, W Dorobek, et al.
Obstetrics and Gynecology|May 8, 1998
Routine ultrasound screening in pregnancy and the children's subsequent neurologic developmentH Kieler, G Ahlsten, B Haglund, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|January 31, 2007
Being born small for gestational age increases the risk of severe pre-eclampsiaK Zetterström, S Lindeberg, B Haglund, et al.
The American Journal of Psychiatry|January 1, 1977
Hydroxyzine in the treatment of alcohol withdrawalS L Dilts, D L Keleher, G Hoge, et al.
International Journal of Obesity (2005)|January 23, 2008
Higher education and more physical activity limit the development of obesity in a Swedish rural population. The Skaraborg ProjectM Nyholm, B Gullberg, B Haglund, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1991
Haplotypes of the steroid 21-hydroxylase gene region encoding mild steroid 21-hydroxylase deficiencyB Haglund-Stengler, E Martin Ritzén, J Gustafsson, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1992
Steroid 21-hydroxylase deficiency: three additional mutated alleles and establishment of phenotype-genotype relationships of common mutationsA Wedell, E M Ritzén, B Haglund-Stengler, et al.
Human Genetics|October 1, 1990
TaqI HLA-B and -DRB RFLP analysis can predict disease in siblings of affected children with 21-hydroxylase deficiencyO Olerup, H Luthman, E M Ritzén, et al.
Pageof 8