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A Wedell

Showing results (11-20 of 54) with videos related to

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Seminars in Fetal & Neonatal Medicine|February 10, 2011
Disorders of sex developmentM Barbaro, A Wedell, A Nordenström
Human Genetics|July 1, 1994
Characterization of mutations on the rare duplicated C4/CYP21 haplotype in steroid 21-hydroxylase deficiencyA Wedell, B Stengler, H Luthman
Hormone Research|July 15, 2000
How can molecular biology contribute to the management of congenital adrenal hyperplasia?E M Ritzén, S Lajic, A Wedell
Journal of Obstetric, Gynecologic, and Neonatal Nursing : JOGNN|July 1, 1985
Endometriosis and the infertile patientM A Wedell, P Billings, J A Fayez
Biochemical and Biophysical Research Communications|April 13, 1999
Effects of missense mutations and deletions on membrane anchoring and enzyme function of human steroid 21-hydroxylase (P450c21)S Lajic, A Nikoshkov, M Holst, et al.
Human Genetics|January 1, 1994
Two new mutations in the porphobilinogen deaminase gene and a screening method using PCR amplification of specific allelesG Lundin, A Wedell, S Thunell, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|April 9, 2008
The reproductive tissue specific cystatin subgroup of genes: expression during gonadal development in wildtype and testatin knockout animalsJ Frygelius, M Oscarson, K Nordqvist, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1997
Synergistic effect of partially inactivating mutations in steroid 21-hydroxylase deficiencyA Nikoshkov, S Lajic, M Holst, et al.
Pediatrics|October 3, 2001
Neonatal screening for congenital adrenal hyperplasia: 17-hydroxyprogesterone levels and CYP21 genotypes in preterm infantsA Nordenström, A Wedell, L Hagenfeldt, et al.
The Journal of Clinical Endocrinology and Metabolism|May 14, 1999
Genotyping is a valuable diagnostic complement to neonatal screening for congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiencyA Nordenström, A Thilén, L Hagenfeldt, et al.
Pageof 6

Showing results (11-20 of 54) with videos related to

Sort By:
Pageof 6
Seminars in Fetal & Neonatal Medicine|February 10, 2011
Disorders of sex developmentM Barbaro, A Wedell, A Nordenström
Human Genetics|July 1, 1994
Characterization of mutations on the rare duplicated C4/CYP21 haplotype in steroid 21-hydroxylase deficiencyA Wedell, B Stengler, H Luthman
Hormone Research|July 15, 2000
How can molecular biology contribute to the management of congenital adrenal hyperplasia?E M Ritzén, S Lajic, A Wedell
Journal of Obstetric, Gynecologic, and Neonatal Nursing : JOGNN|July 1, 1985
Endometriosis and the infertile patientM A Wedell, P Billings, J A Fayez
Biochemical and Biophysical Research Communications|April 13, 1999
Effects of missense mutations and deletions on membrane anchoring and enzyme function of human steroid 21-hydroxylase (P450c21)S Lajic, A Nikoshkov, M Holst, et al.
Human Genetics|January 1, 1994
Two new mutations in the porphobilinogen deaminase gene and a screening method using PCR amplification of specific allelesG Lundin, A Wedell, S Thunell, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|April 9, 2008
The reproductive tissue specific cystatin subgroup of genes: expression during gonadal development in wildtype and testatin knockout animalsJ Frygelius, M Oscarson, K Nordqvist, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1997
Synergistic effect of partially inactivating mutations in steroid 21-hydroxylase deficiencyA Nikoshkov, S Lajic, M Holst, et al.
Pediatrics|October 3, 2001
Neonatal screening for congenital adrenal hyperplasia: 17-hydroxyprogesterone levels and CYP21 genotypes in preterm infantsA Nordenström, A Wedell, L Hagenfeldt, et al.
The Journal of Clinical Endocrinology and Metabolism|May 14, 1999
Genotyping is a valuable diagnostic complement to neonatal screening for congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiencyA Nordenström, A Thilén, L Hagenfeldt, et al.
Pageof 6