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Clinical Genetics
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July 1, 1990
Ratio of fetal to maternal DNA is less than 1 in 5000 at different gestational ages in maternal blood
D Gänshirt-Ahlert, M Pohlschmidt, A Gal, et al.
Annals of the New York Academy of Sciences
|
September 7, 1994
Noninvasive prenatal diagnosis. Strategy for a clinical trial
W Holzgreve, H S Garritsen, S Tercanli, et al.
Klinische Padiatrie
|
May 1, 1997
[A rare combination of partial trisomy 9 with pulmonary atresia]
T Nekarda, D Kececioglu, H G Kehl, et al.
Prenatal Diagnosis
|
March 1, 1993
First-trimester alpha-fetoprotein screening for Down syndrome
W Fuhrmann, K Altland, V Jovanovic, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
April 26, 2001
Fanconi anemia associated with increased nuchal translucency detected by first-trimester ultrasound
S Tercanli, P Miny, M S Siebert, et al.
Clinical Genetics
|
August 1, 1995
Congenital heart disease in the 48,XXYY syndrome
D Meschede, T Nekarda, D Kececioglu, et al.
Geburtshilfe Und Frauenheilkunde
|
August 1, 1987
[Experiences with prenatal diagnosis of sickle cell anemia and thalassemias in the first trimester of pregnancy: various aspects for the obstetrician]
W Holzgreve, C Aulehla-Scholz, E U Griese, et al.
Geburtshilfe Und Frauenheilkunde
|
May 1, 1986
[Chromosome studies of chorionic villi: experiences following 118 diagnostic interventions]
P Miny, W Holzgreve, S Basaran, et al.
Geburtshilfe Und Frauenheilkunde
|
September 1, 1991
[Prenatal diagnosis with chorionic villi and placenta puncture biopsy in the 1st to 3d trimester of pregnancy: diagnostic value of chromosome studies]
P Miny, P Hammer, R Schloo, et al.
Prenatal Diagnosis
|
October 1, 1988
False negative cytogenetic result in direct preparations after CVS
P Miny, S Basaran, W Holzgreve, et al.
Page
of 9
Search research articles
Search
Showing results (51-60 of 83) with videos related to
Sort By:
Page
of 9
Clinical Genetics
|
July 1, 1990
Ratio of fetal to maternal DNA is less than 1 in 5000 at different gestational ages in maternal blood
D Gänshirt-Ahlert, M Pohlschmidt, A Gal, et al.
Annals of the New York Academy of Sciences
|
September 7, 1994
Noninvasive prenatal diagnosis. Strategy for a clinical trial
W Holzgreve, H S Garritsen, S Tercanli, et al.
Klinische Padiatrie
|
May 1, 1997
[A rare combination of partial trisomy 9 with pulmonary atresia]
T Nekarda, D Kececioglu, H G Kehl, et al.
Prenatal Diagnosis
|
March 1, 1993
First-trimester alpha-fetoprotein screening for Down syndrome
W Fuhrmann, K Altland, V Jovanovic, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
April 26, 2001
Fanconi anemia associated with increased nuchal translucency detected by first-trimester ultrasound
S Tercanli, P Miny, M S Siebert, et al.
Clinical Genetics
|
August 1, 1995
Congenital heart disease in the 48,XXYY syndrome
D Meschede, T Nekarda, D Kececioglu, et al.
Geburtshilfe Und Frauenheilkunde
|
August 1, 1987
[Experiences with prenatal diagnosis of sickle cell anemia and thalassemias in the first trimester of pregnancy: various aspects for the obstetrician]
W Holzgreve, C Aulehla-Scholz, E U Griese, et al.
Geburtshilfe Und Frauenheilkunde
|
May 1, 1986
[Chromosome studies of chorionic villi: experiences following 118 diagnostic interventions]
P Miny, W Holzgreve, S Basaran, et al.
Geburtshilfe Und Frauenheilkunde
|
September 1, 1991
[Prenatal diagnosis with chorionic villi and placenta puncture biopsy in the 1st to 3d trimester of pregnancy: diagnostic value of chromosome studies]
P Miny, P Hammer, R Schloo, et al.
Prenatal Diagnosis
|
October 1, 1988
False negative cytogenetic result in direct preparations after CVS
P Miny, S Basaran, W Holzgreve, et al.
Page
of 9