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A Wedell

Showing results (1-10 of 54) with videos related to

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Acta Paediatrica (Oslo, Norway : 1992)|March 25, 1998
Molecular genetics of congenital adrenal hyperplasia (21-hydroxylase deficiency): implications for diagnosis, prognosis and treatmentA Wedell
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 26, 1998
An update on the molecular genetics of congenital adrenal hyperplasia: diagnostic and therapeutic aspectsA Wedell
Clinics in Laboratory Medicine|March 1, 1996
Molecular approaches for the diagnosis of 21-hydroxylase deficiency and congenital adrenal hyperplasiaA Wedell
Human Molecular Genetics|May 1, 1993
Steroid 21-hydroxylase deficiency: two additional mutations in salt-wasting disease and rapid screening of disease-causing mutationsA Wedell, H Luthman
Human Genetics|April 1, 1993
Steroid 21-hydroxylase (P450c21): a new allele and spread of mutations through the pseudogeneA Wedell, H Luthman
Human Genetics|August 1, 1996
An intron 1 splice mutation and a nonsense mutation (W23X) in CYP21 causing severe congenital adrenal hyperplasiaS Lajic, A Wedell
Journal of Internal Medicine|August 8, 2015
Exome and genome sequencing: a revolution for the discovery and diagnosis of monogenic disordersH Stranneheim, A Wedell
Journal of Internal Medicine|May 15, 2020
Mitochondria in human diseaseN-G Larsson, A Wedell
Human Genetics|February 1, 1994
A steroid 21-hydroxylase allele concomitantly carrying four disease-causing mutations is not uncommon in the swedish populationA Wedell, X Chun, H Luthman
Lakartidningen|March 9, 2000
[Boy or girl? Molecular mechanisms in sex differentiation]A Wedell, M Ritzén, A Nordenskjöld
Pageof 6

Showing results (1-10 of 54) with videos related to

Sort By:
Pageof 6
Acta Paediatrica (Oslo, Norway : 1992)|March 25, 1998
Molecular genetics of congenital adrenal hyperplasia (21-hydroxylase deficiency): implications for diagnosis, prognosis and treatmentA Wedell
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 26, 1998
An update on the molecular genetics of congenital adrenal hyperplasia: diagnostic and therapeutic aspectsA Wedell
Clinics in Laboratory Medicine|March 1, 1996
Molecular approaches for the diagnosis of 21-hydroxylase deficiency and congenital adrenal hyperplasiaA Wedell
Human Molecular Genetics|May 1, 1993
Steroid 21-hydroxylase deficiency: two additional mutations in salt-wasting disease and rapid screening of disease-causing mutationsA Wedell, H Luthman
Human Genetics|April 1, 1993
Steroid 21-hydroxylase (P450c21): a new allele and spread of mutations through the pseudogeneA Wedell, H Luthman
Human Genetics|August 1, 1996
An intron 1 splice mutation and a nonsense mutation (W23X) in CYP21 causing severe congenital adrenal hyperplasiaS Lajic, A Wedell
Journal of Internal Medicine|August 8, 2015
Exome and genome sequencing: a revolution for the discovery and diagnosis of monogenic disordersH Stranneheim, A Wedell
Journal of Internal Medicine|May 15, 2020
Mitochondria in human diseaseN-G Larsson, A Wedell
Human Genetics|February 1, 1994
A steroid 21-hydroxylase allele concomitantly carrying four disease-causing mutations is not uncommon in the swedish populationA Wedell, X Chun, H Luthman
Lakartidningen|March 9, 2000
[Boy or girl? Molecular mechanisms in sex differentiation]A Wedell, M Ritzén, A Nordenskjöld
Pageof 6