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D Gänshirt

Showing results (1-10 of 11) with videos related to

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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 bloodD 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 chromosomeD Gänshirt-Ahlert, I H Pawlowitzki, A Gal
Obstetrics and Gynecology|October 1, 1992
Fetal DNA in uterine vein bloodD 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 bloodD Gänshirt-Ahlert, M Pohlschmidt, A Gal, et al.
Obstetrics and Gynecology|May 8, 1998
Disturbed feto-maternal cell traffic in preeclampsiaW 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 bloodD 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 sortingD Gänshirt-Ahlert, R Börjesson-Stoll, M Burschyk, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 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 bloodD 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 chromosomeD Gänshirt-Ahlert, I H Pawlowitzki, A Gal
Obstetrics and Gynecology|October 1, 1992
Fetal DNA in uterine vein bloodD 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 bloodD Gänshirt-Ahlert, M Pohlschmidt, A Gal, et al.
Obstetrics and Gynecology|May 8, 1998
Disturbed feto-maternal cell traffic in preeclampsiaW 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 bloodD 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 sortingD Gänshirt-Ahlert, R Börjesson-Stoll, M Burschyk, et al.
Pageof 2