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F Skovby

Showing results (1-10 of 116) with videos related to

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Ugeskrift for Laeger|August 27, 1973
[Chromosome identification and chromosome disease]F Skovby
Ugeskrift for Laeger|October 23, 1998
[Neonatal screening for hereditary diseases]F Skovby
Ugeskrift for Laeger|January 1, 1977
[Vitamin D-resistant hypophosphatemic rickets]F Skovby
Ugeskrift for Laeger|January 16, 1999
[Treatment of hereditary and malignant diseases by regulating genetic transcription?]F Skovby
Ugeskrift for Laeger|March 17, 1986
[Genetic diagnosis and counseling in perinatal death]F Skovby
Haemostasis|January 1, 1989
Inborn errors of metabolism causing homocysteinemia and related vascular involvementF Skovby
Ugeskrift for Laeger|October 23, 2001
[Dysmorphic children]F Skovby
Clinical Genetics|January 1, 1975
Nomenclature: additional chromosome bandsF Skovby
Ugeskrift for Laeger|October 31, 1988
[Hyperammonemia in children]F Skovby
Acta Paediatrica Scandinavica. Supplement|January 1, 1985
Homocystinuria. Clinical, biochemical and genetic aspects of cystathionine beta-synthase and its deficiency in manF Skovby
Pageof 12

Showing results (1-10 of 116) with videos related to

Sort By:
Pageof 12
Ugeskrift for Laeger|August 27, 1973
[Chromosome identification and chromosome disease]F Skovby
Ugeskrift for Laeger|October 23, 1998
[Neonatal screening for hereditary diseases]F Skovby
Ugeskrift for Laeger|January 1, 1977
[Vitamin D-resistant hypophosphatemic rickets]F Skovby
Ugeskrift for Laeger|January 16, 1999
[Treatment of hereditary and malignant diseases by regulating genetic transcription?]F Skovby
Ugeskrift for Laeger|March 17, 1986
[Genetic diagnosis and counseling in perinatal death]F Skovby
Haemostasis|January 1, 1989
Inborn errors of metabolism causing homocysteinemia and related vascular involvementF Skovby
Ugeskrift for Laeger|October 23, 2001
[Dysmorphic children]F Skovby
Clinical Genetics|January 1, 1975
Nomenclature: additional chromosome bandsF Skovby
Ugeskrift for Laeger|October 31, 1988
[Hyperammonemia in children]F Skovby
Acta Paediatrica Scandinavica. Supplement|January 1, 1985
Homocystinuria. Clinical, biochemical and genetic aspects of cystathionine beta-synthase and its deficiency in manF Skovby
Pageof 12