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Thrombosis and Haemostasis
|
December 18, 1987
Combined use of DNA probes in first-trimester prenatal diagnosis of hemophilia A
M Sampietro, G Camerino, M Romano, et al.
Acta Universitatis Carolinae. Medica
|
January 1, 1990
Prevention of cystic fibrosis in Italian families by DNA studies
M Ferrari, L Cremonesi, L Ruocco, et al.
Current Studies in Hematology and Blood Transfusion
|
January 1, 1991
Prenatal diagnosis and carrier detection of hemophilia A
M Sampietro, E Sacchi, A M Randi, et al.
British Journal of Obstetrics and Gynaecology
|
April 1, 1993
Low maternal serum levels of pregnancy associated plasma protein A (PAPP-A) in the first trimester in association with abnormal fetal karyotype
B Brambati, M C Macintosh, B Teisner, et al.
Prenatal Diagnosis
|
March 1, 1993
Risk evaluation of CVS
A M Kuliev, B Modell, L Jackson, et al.
Journal of Assisted Reproduction and Genetics
|
August 1, 1992
Chorionic villus sampling (CVS): World Health Organization European Regional Office (WHO/EURO) meeting statement on the use of CVS in prenatal diagnosis
A M Kuliev, B Modell, L Jackson, et al.
Lancet (London, England)
|
October 8, 1988
First-trimester biochemical screening for Down syndrome
H S Cuckle, N J Wald, G Barkai, et al.
Human Reproduction (Oxford, England)
|
June 1, 1995
The Euro-Team Early Pregnancy (ETEP) protocol for recurrent miscarriage
C W Berry, B Brambati, T K Eskes, et al.
Medicine, Health Care, and Philosophy
|
April 17, 2002
Ethical guidance on human embryonic and fetal tissue transplantation: a European overview
Wert G de, R L Berghmans, G J Boer, et al.
Neuromuscular Disorders : NMD
|
June 26, 1999
Molecular analysis of 4q35 rearrangements in fascioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the disease
G Galluzzi, G Deidda, S Cacurri, et al.
Page
of 12
Search research articles
Search
Showing results (101-110 of 114) with videos related to
Sort By:
Page
of 12
Thrombosis and Haemostasis
|
December 18, 1987
Combined use of DNA probes in first-trimester prenatal diagnosis of hemophilia A
M Sampietro, G Camerino, M Romano, et al.
Acta Universitatis Carolinae. Medica
|
January 1, 1990
Prevention of cystic fibrosis in Italian families by DNA studies
M Ferrari, L Cremonesi, L Ruocco, et al.
Current Studies in Hematology and Blood Transfusion
|
January 1, 1991
Prenatal diagnosis and carrier detection of hemophilia A
M Sampietro, E Sacchi, A M Randi, et al.
British Journal of Obstetrics and Gynaecology
|
April 1, 1993
Low maternal serum levels of pregnancy associated plasma protein A (PAPP-A) in the first trimester in association with abnormal fetal karyotype
B Brambati, M C Macintosh, B Teisner, et al.
Prenatal Diagnosis
|
March 1, 1993
Risk evaluation of CVS
A M Kuliev, B Modell, L Jackson, et al.
Journal of Assisted Reproduction and Genetics
|
August 1, 1992
Chorionic villus sampling (CVS): World Health Organization European Regional Office (WHO/EURO) meeting statement on the use of CVS in prenatal diagnosis
A M Kuliev, B Modell, L Jackson, et al.
Lancet (London, England)
|
October 8, 1988
First-trimester biochemical screening for Down syndrome
H S Cuckle, N J Wald, G Barkai, et al.
Human Reproduction (Oxford, England)
|
June 1, 1995
The Euro-Team Early Pregnancy (ETEP) protocol for recurrent miscarriage
C W Berry, B Brambati, T K Eskes, et al.
Medicine, Health Care, and Philosophy
|
April 17, 2002
Ethical guidance on human embryonic and fetal tissue transplantation: a European overview
Wert G de, R L Berghmans, G J Boer, et al.
Neuromuscular Disorders : NMD
|
June 26, 1999
Molecular analysis of 4q35 rearrangements in fascioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the disease
G Galluzzi, G Deidda, S Cacurri, et al.
Page
of 12