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F Z Bischoff

Showing results (11-20 of 30) with videos related to

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Human Molecular Genetics|March 1, 1995
Single cell analysis demonstrating somatic mosaicism involving 11p in a patient with paternal isodisomy and Beckwith-Wiedemann syndromeF Z Bischoff, G L Feldman, C McCaskill, et al.
Fertility and Sterility|November 13, 2001
Increased chromosome X, Y, and 18 nondisjunction in sperm from infertile patients that were identified as normal by strict morphology: implication for intracytoplasmic sperm injectionH M Ryu, W W Lin, D J Lamb, et al.
Journal of the Society for Gynecologic Investigation|April 17, 1999
Noninvasive determination of fetal RhD status using fetal DNA in maternal serum and PCRF Z Bischoff, D D Nguyen, D Marquéz-Do, et al.
American Journal of Medical Genetics|June 28, 2001
Evidence of skewed X-chromosome inactivation in 47,XXY and 48,XXYY Klinefelter patientsY Iitsuka, A Bock, D D Nguyen, et al.
American Journal of Medical Genetics|December 11, 1996
Comprehensive 4-year follow-up on a case of maternal heterodisomy for chromosome 16A S Schneider, F Z Bischoff, C McCaskill, et al.
Clinical Genetics|June 6, 2003
Intact fetal cell isolation from maternal blood: improved isolation using a simple whole blood progenitor cell enrichment approach (RosetteSep)F Z Bischoff, D A Marquéz-Do, D I Martinez, et al.
American Journal of Obstetrics and Gynecology|April 16, 1999
Increased heterogeneity of chromosome 17 aneuploidy in endometriosisY Kosugi, S Elias, L R Malinak, et al.
Human Genetics|September 1, 1997
Detection of chromosomal aneuploidy in endometriosis by multi-color fluorescence in situ hybridization (FISH)J C Shin, H L Ross, S Elias, et al.
Prenatal Diagnosis|December 1, 1995
Detection of low-grade mosaicism in fetal cells isolated from maternal bloodF Z Bischoff, D E Lewis, J L Simpson, et al.
American Journal of Obstetrics and Gynecology|August 15, 1998
Prenatal diagnosis with use of fetal cells isolated from maternal blood: five-color fluorescent in situ hybridization analysis on flow-sorted cells for chromosomes X, Y, 13, 18, and 21F Z Bischoff, D E Lewis, D D Nguyen, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
Human Molecular Genetics|March 1, 1995
Single cell analysis demonstrating somatic mosaicism involving 11p in a patient with paternal isodisomy and Beckwith-Wiedemann syndromeF Z Bischoff, G L Feldman, C McCaskill, et al.
Fertility and Sterility|November 13, 2001
Increased chromosome X, Y, and 18 nondisjunction in sperm from infertile patients that were identified as normal by strict morphology: implication for intracytoplasmic sperm injectionH M Ryu, W W Lin, D J Lamb, et al.
Journal of the Society for Gynecologic Investigation|April 17, 1999
Noninvasive determination of fetal RhD status using fetal DNA in maternal serum and PCRF Z Bischoff, D D Nguyen, D Marquéz-Do, et al.
American Journal of Medical Genetics|June 28, 2001
Evidence of skewed X-chromosome inactivation in 47,XXY and 48,XXYY Klinefelter patientsY Iitsuka, A Bock, D D Nguyen, et al.
American Journal of Medical Genetics|December 11, 1996
Comprehensive 4-year follow-up on a case of maternal heterodisomy for chromosome 16A S Schneider, F Z Bischoff, C McCaskill, et al.
Clinical Genetics|June 6, 2003
Intact fetal cell isolation from maternal blood: improved isolation using a simple whole blood progenitor cell enrichment approach (RosetteSep)F Z Bischoff, D A Marquéz-Do, D I Martinez, et al.
American Journal of Obstetrics and Gynecology|April 16, 1999
Increased heterogeneity of chromosome 17 aneuploidy in endometriosisY Kosugi, S Elias, L R Malinak, et al.
Human Genetics|September 1, 1997
Detection of chromosomal aneuploidy in endometriosis by multi-color fluorescence in situ hybridization (FISH)J C Shin, H L Ross, S Elias, et al.
Prenatal Diagnosis|December 1, 1995
Detection of low-grade mosaicism in fetal cells isolated from maternal bloodF Z Bischoff, D E Lewis, J L Simpson, et al.
American Journal of Obstetrics and Gynecology|August 15, 1998
Prenatal diagnosis with use of fetal cells isolated from maternal blood: five-color fluorescent in situ hybridization analysis on flow-sorted cells for chromosomes X, Y, 13, 18, and 21F Z Bischoff, D E Lewis, D D Nguyen, et al.
Pageof 3