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N J BRANDT

Showing results (21-30 of 52) with videos related to

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Ugeskrift for Laeger|October 23, 1998
[Neonatal screening in Denmark. Status and future perspectives]H Simonsen, N J Brandt, B Nørgaard-Pedersen
Journal of Inherited Metabolic Disease|January 1, 1981
Formiminoglutamic aciduria in a slightly retarded boy with chronic obstructive lung diseaseB Beck, E Christensen, N J Brandt, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Psychological impact of carrier screening for cystic fibrosis among pregnant womenH Clausen, N J Brandt, M Schwartz, et al.
Prenatal Diagnosis|July 1, 1985
Exclusion of citrullinaemia in the first trimester of pregnancy by direct assay of argininosuccinate synthetase in chorionic villiE Christensen, N J Brandt, J Philip, et al.
Ugeskrift for Laeger|August 12, 1996
[A follow-up study of carriers of cystic fibrosis]N J Brandt, M Schwartz, F Skovby, et al.
Clinical Genetics|April 1, 1996
Psychological and social impact of carrier screening for cystic fibrosis among pregnant woman--a pilot studyH Clausen, N J Brandt, M Schwartz, et al.
Human Genetics|May 26, 1998
The human glutaryl-CoA dehydrogenase gene: report of intronic sequences and of 13 novel mutations causing glutaric aciduria type IM Schwartz, E Christensen, A Superti-Furga, et al.
Journal of Inherited Metabolic Disease|January 1, 1980
Citrullinaemia: the possibility of prenatal diagnosisE Christensen, N J Brandt, J Philip, et al.
Human Genetics|September 1, 1990
Frequency of the delta F508 mutation on cystic fibrosis chromosomes in DenmarkM Schwartz, H K Johansen, C Koch, et al.
Clinical Genetics|December 1, 1978
ABO and Rh phenotyping of foetal blood obtained by foetoscopyJ Philip, N J Brandt, A Fernandes, et al.
Pageof 6

Showing results (21-30 of 52) with videos related to

Sort By:
Pageof 6
Ugeskrift for Laeger|October 23, 1998
[Neonatal screening in Denmark. Status and future perspectives]H Simonsen, N J Brandt, B Nørgaard-Pedersen
Journal of Inherited Metabolic Disease|January 1, 1981
Formiminoglutamic aciduria in a slightly retarded boy with chronic obstructive lung diseaseB Beck, E Christensen, N J Brandt, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Psychological impact of carrier screening for cystic fibrosis among pregnant womenH Clausen, N J Brandt, M Schwartz, et al.
Prenatal Diagnosis|July 1, 1985
Exclusion of citrullinaemia in the first trimester of pregnancy by direct assay of argininosuccinate synthetase in chorionic villiE Christensen, N J Brandt, J Philip, et al.
Ugeskrift for Laeger|August 12, 1996
[A follow-up study of carriers of cystic fibrosis]N J Brandt, M Schwartz, F Skovby, et al.
Clinical Genetics|April 1, 1996
Psychological and social impact of carrier screening for cystic fibrosis among pregnant woman--a pilot studyH Clausen, N J Brandt, M Schwartz, et al.
Human Genetics|May 26, 1998
The human glutaryl-CoA dehydrogenase gene: report of intronic sequences and of 13 novel mutations causing glutaric aciduria type IM Schwartz, E Christensen, A Superti-Furga, et al.
Journal of Inherited Metabolic Disease|January 1, 1980
Citrullinaemia: the possibility of prenatal diagnosisE Christensen, N J Brandt, J Philip, et al.
Human Genetics|September 1, 1990
Frequency of the delta F508 mutation on cystic fibrosis chromosomes in DenmarkM Schwartz, H K Johansen, C Koch, et al.
Clinical Genetics|December 1, 1978
ABO and Rh phenotyping of foetal blood obtained by foetoscopyJ Philip, N J Brandt, A Fernandes, et al.
Pageof 6