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Family Planning Perspectives
|
May 2, 2001
Teenage childbearing and long-term socioeconomic consequences: a case study in Sweden
P 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 study
A 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 gene
E 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 development
H 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-eclampsia
K Zetterström, S Lindeberg, B Haglund, et al.
The American Journal of Psychiatry
|
January 1, 1977
Hydroxyzine in the treatment of alcohol withdrawal
S 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 Project
M 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 deficiency
B 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 mutations
A 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 deficiency
O Olerup, H Luthman, E M Ritzén, et al.
Page
of 8
Search research articles
Search
Showing results (51-60 of 79) with videos related to
Sort By:
Page
of 8
Family Planning Perspectives
|
May 2, 2001
Teenage childbearing and long-term socioeconomic consequences: a case study in Sweden
P 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 study
A 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 gene
E 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 development
H 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-eclampsia
K Zetterström, S Lindeberg, B Haglund, et al.
The American Journal of Psychiatry
|
January 1, 1977
Hydroxyzine in the treatment of alcohol withdrawal
S 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 Project
M 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 deficiency
B 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 mutations
A 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 deficiency
O Olerup, H Luthman, E M Ritzén, et al.
Page
of 8