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C H Rodeck

Showing results (301-310 of 324) with videos related to

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British Journal of Obstetrics and Gynaecology|September 1, 1983
Erythropoietin and cord blood haemoglobin in the regulation of human fetal erythropoiesisR M Thomas, C E Canning, P M Cotes, et al.
Lancet (London, England)|November 8, 1980
Dual diagnosis of prenatal haemophilia A by measurement of fetal factor VIIIC and VIIIC antigen (VIIICAg)R S Mibashan, I R Peake, C H Rodeck, et al.
Lancet (London, England)|June 21, 1986
First-trimester prenatal diagnosis of cystic fibrosis with linked DNA probesM Farrall, H Y Law, C H Rodeck, et al.
Immunology Letters|April 1, 1989
On the feasibility of inducing tolerance in man: a study in the cynomolgus monkeyL Brent, D C Linch, C H Rodeck, et al.
Journal of Medical Genetics|September 1, 1995
Use of type VII collagen gene (COL7A1) markers in prenatal diagnosis of recessive dystrophic epidermolysis bullosaM G Dunnill, C H Rodeck, A J Richards, et al.
Prenatal Diagnosis|July 1, 1995
Genetic basis of lethal junctional epidermolysis bullosa in an affected fetus: implications for prenatal diagnosis in one familyJ A McGrath, J R McMillan, M G Dunnill, et al.
British Journal of Obstetrics and Gynaecology|December 16, 1998
Intra-amniotic inflammation in human gastroschisis: possible aetiology of postnatal bowel dysfunctionJ J Morrison, N Klein, L S Chitty, et al.
Ultrasound in Medicine & Biology|April 11, 2001
Online motion-gated dynamic three-dimensional echocardiography in the fetus--preliminary resultsJ Deng, R Yates, A G Birkett, et al.
Genomics|September 1, 1995
A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5 (LAMA3) in Herlitz junctional epidermolysis bullosa: prenatal exclusion in a fetus at riskJ A McGrath, S Kivirikko, S Ciatti, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Experience with prenatal diagnosis of propionic acidaemia and methylmalonic aciduriaA H Fensom, P F Benson, R A Chalmers, et al.
Pageof 33

Showing results (301-310 of 324) with videos related to

Sort By:
Pageof 33
British Journal of Obstetrics and Gynaecology|September 1, 1983
Erythropoietin and cord blood haemoglobin in the regulation of human fetal erythropoiesisR M Thomas, C E Canning, P M Cotes, et al.
Lancet (London, England)|November 8, 1980
Dual diagnosis of prenatal haemophilia A by measurement of fetal factor VIIIC and VIIIC antigen (VIIICAg)R S Mibashan, I R Peake, C H Rodeck, et al.
Lancet (London, England)|June 21, 1986
First-trimester prenatal diagnosis of cystic fibrosis with linked DNA probesM Farrall, H Y Law, C H Rodeck, et al.
Immunology Letters|April 1, 1989
On the feasibility of inducing tolerance in man: a study in the cynomolgus monkeyL Brent, D C Linch, C H Rodeck, et al.
Journal of Medical Genetics|September 1, 1995
Use of type VII collagen gene (COL7A1) markers in prenatal diagnosis of recessive dystrophic epidermolysis bullosaM G Dunnill, C H Rodeck, A J Richards, et al.
Prenatal Diagnosis|July 1, 1995
Genetic basis of lethal junctional epidermolysis bullosa in an affected fetus: implications for prenatal diagnosis in one familyJ A McGrath, J R McMillan, M G Dunnill, et al.
British Journal of Obstetrics and Gynaecology|December 16, 1998
Intra-amniotic inflammation in human gastroschisis: possible aetiology of postnatal bowel dysfunctionJ J Morrison, N Klein, L S Chitty, et al.
Ultrasound in Medicine & Biology|April 11, 2001
Online motion-gated dynamic three-dimensional echocardiography in the fetus--preliminary resultsJ Deng, R Yates, A G Birkett, et al.
Genomics|September 1, 1995
A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5 (LAMA3) in Herlitz junctional epidermolysis bullosa: prenatal exclusion in a fetus at riskJ A McGrath, S Kivirikko, S Ciatti, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Experience with prenatal diagnosis of propionic acidaemia and methylmalonic aciduriaA H Fensom, P F Benson, R A Chalmers, et al.
Pageof 33