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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.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)
|
October 11, 2007
[Prenatal diagnosis of diastematomyelia and tethered cord - a case report and review of the literature]
H Struben, E Visca, W Holzgreve, 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.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
November 9, 2002
Bedside estimation of Down syndrome risk during first-trimester ultrasound screening
A Herman, E Dreazen, A M Herman, et al.
Molecular Human Reproduction
|
December 10, 1999
Approximately half of the erythroblasts in maternal blood are of fetal origin
C Troeger, X Y Zhong, R Burgemeister, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)
|
April 5, 2022
The Fetal Medicine Foundation (FMF) Germany after 20 Years - Quality Assurance of Ultrasound Examinations during First Trimester Screening
E Merz, Ch Thode, B J Hackelöer, et al.
American Journal of Medical Genetics
|
May 22, 1995
Parental origin of the extra haploid chromosome set in triploidies diagnosed prenatally
P Miny, B Koppers, B Dworniczak, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)
|
April 20, 2016
Quality Requirements for the early Fetal Ultrasound Assessment at 11-13+6 Weeks of Gestation (DEGUM Levels II and III)
C von Kaisenberg, R Chaoui, M Häusler, et al.
Clinical Genetics
|
October 17, 2013
Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype
I Filges, E Nosova, E Bruder, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)
|
October 16, 2015
Cell-Free DNA Testing for Fetal Chromosomal Anomalies in clinical practice: Austrian-German-Swiss Recommendations for non-invasive prenatal tests (NIPT)
M Schmid, P Klaritsch, W Arzt, et al.
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of 8
Search research articles
Search
Showing results (61-70 of 74) with videos related to
Sort By:
Page
of 8
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.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)
|
October 11, 2007
[Prenatal diagnosis of diastematomyelia and tethered cord - a case report and review of the literature]
H Struben, E Visca, W Holzgreve, 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.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
November 9, 2002
Bedside estimation of Down syndrome risk during first-trimester ultrasound screening
A Herman, E Dreazen, A M Herman, et al.
Molecular Human Reproduction
|
December 10, 1999
Approximately half of the erythroblasts in maternal blood are of fetal origin
C Troeger, X Y Zhong, R Burgemeister, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)
|
April 5, 2022
The Fetal Medicine Foundation (FMF) Germany after 20 Years - Quality Assurance of Ultrasound Examinations during First Trimester Screening
E Merz, Ch Thode, B J Hackelöer, et al.
American Journal of Medical Genetics
|
May 22, 1995
Parental origin of the extra haploid chromosome set in triploidies diagnosed prenatally
P Miny, B Koppers, B Dworniczak, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)
|
April 20, 2016
Quality Requirements for the early Fetal Ultrasound Assessment at 11-13+6 Weeks of Gestation (DEGUM Levels II and III)
C von Kaisenberg, R Chaoui, M Häusler, et al.
Clinical Genetics
|
October 17, 2013
Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype
I Filges, E Nosova, E Bruder, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)
|
October 16, 2015
Cell-Free DNA Testing for Fetal Chromosomal Anomalies in clinical practice: Austrian-German-Swiss Recommendations for non-invasive prenatal tests (NIPT)
M Schmid, P Klaritsch, W Arzt, et al.
Page
of 8