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Human Genetics
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January 1, 1984
Hae III restriction of DNA from three cases with nonfluorescent Y chromosomes (45XO/46XYnf)
D Gänshirt, I H Pawlowitzki
Current Opinion in Obstetrics & Gynecology
|
April 1, 1995
Fetal cells in maternal blood
D Gänshirt, H S Garritsen, W Holzgreve
Therapeutische Umschau. Revue Therapeutique
|
December 1, 1995
[Prenatal diagnosis]
P Miny, S Tercanli, D Gänshirt, et al.
Human Genetics
|
June 1, 1987
Three cases of 45,X/46,XYnf mosaicism. Molecular analysis revealed heterogeneity of the nonfluorescent Y chromosome
D Gänshirt-Ahlert, I H Pawlowitzki, A Gal
Obstetrics and Gynecology
|
October 1, 1992
Fetal DNA in uterine vein blood
D Gänshirt-Ahlert, N Basak, K Aidynli, et al.
Obstetrics and Gynecology
|
March 1, 1990
Transabdominal placental biopsy in the second and third trimesters of pregnancy: what is the risk of maternal contamination in DNA diagnosis?
D Gänshirt-Ahlert, M Pohlschmidt, A Gal, et al.
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.
Obstetrics and Gynecology
|
May 8, 1998
Disturbed feto-maternal cell traffic in preeclampsia
W Holzgreve, F Ghezzi, E Di Naro, et al.
American Journal of Obstetrics and Gynecology
|
May 1, 1992
Magnetic cell sorting and the transferrin receptor as potential means of prenatal diagnosis from maternal blood
D Gänshirt-Ahlert, M Burschyk, H S Garritsen, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)
|
September 1, 1993
Detection of fetal trisomies 21 and 18 from maternal blood using triple gradient and magnetic cell sorting
D Gänshirt-Ahlert, R Börjesson-Stoll, M Burschyk, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Human Genetics
|
January 1, 1984
Hae III restriction of DNA from three cases with nonfluorescent Y chromosomes (45XO/46XYnf)
D Gänshirt, I H Pawlowitzki
Current Opinion in Obstetrics & Gynecology
|
April 1, 1995
Fetal cells in maternal blood
D Gänshirt, H S Garritsen, W Holzgreve
Therapeutische Umschau. Revue Therapeutique
|
December 1, 1995
[Prenatal diagnosis]
P Miny, S Tercanli, D Gänshirt, et al.
Human Genetics
|
June 1, 1987
Three cases of 45,X/46,XYnf mosaicism. Molecular analysis revealed heterogeneity of the nonfluorescent Y chromosome
D Gänshirt-Ahlert, I H Pawlowitzki, A Gal
Obstetrics and Gynecology
|
October 1, 1992
Fetal DNA in uterine vein blood
D Gänshirt-Ahlert, N Basak, K Aidynli, et al.
Obstetrics and Gynecology
|
March 1, 1990
Transabdominal placental biopsy in the second and third trimesters of pregnancy: what is the risk of maternal contamination in DNA diagnosis?
D Gänshirt-Ahlert, M Pohlschmidt, A Gal, et al.
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.
Obstetrics and Gynecology
|
May 8, 1998
Disturbed feto-maternal cell traffic in preeclampsia
W Holzgreve, F Ghezzi, E Di Naro, et al.
American Journal of Obstetrics and Gynecology
|
May 1, 1992
Magnetic cell sorting and the transferrin receptor as potential means of prenatal diagnosis from maternal blood
D Gänshirt-Ahlert, M Burschyk, H S Garritsen, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)
|
September 1, 1993
Detection of fetal trisomies 21 and 18 from maternal blood using triple gradient and magnetic cell sorting
D Gänshirt-Ahlert, R Börjesson-Stoll, M Burschyk, et al.
Page
of 2