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W Klinger

Showing results (201-210 of 251) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 3, 2001
Laboratory standards and guidelines for population-based cystic fibrosis carrier screeningW W Grody, G R Cutting, K W Klinger, et al.
Human Molecular Genetics|June 22, 2000
Strong homophilic interactions of the Ig-like domains of polycystin-1, the protein product of an autosomal dominant polycystic kidney disease gene, PKD1O Ibraghimov-Beskrovnaya, N O Bukanov, L C Donohue, et al.
American Journal of Obstetrics and Gynecology|December 1, 1992
Rapid prenatal diagnosis by fluorescent in situ hybridization of chorionic villi: an adjunct to long-term culture and karyotypeM I Evans, K W Klinger, N B Isada, et al.
American Journal of Human Genetics|October 23, 1997
PCR quantitation of fetal cells in maternal blood in normal and aneuploid pregnanciesD W Bianchi, J M Williams, L M Sullivan, et al.
Experimental Cell Research|December 20, 2008
Netrin-4 regulates angiogenic responses and tumor cell growthMariana Nacht, Thia B St Martin, Ann Byrne, et al.
Genomics|April 15, 1997
The NTN2L gene encoding a novel human netrin maps to the autosomal dominant polycystic kidney disease region on chromosome 16p13.3T J Van Raay, S M Foskett, T D Connors, et al.
American Journal of Obstetrics and Gynecology|March 23, 2001
Significant fetal-maternal hemorrhage after termination of pregnancy: implications for development of fetal cell microchimerismD W Bianchi, A Farina, W Weber, et al.
Genomics|January 15, 1997
The cloning of a human ABC gene (ABC3) mapping to chromosome 16p13.3T D Connors, T J Van Raay, L R Petry, et al.
Fetal Diagnosis and Therapy|November 1, 1994
Fluorescent in situ hybridization and second-trimester sonographic anomalies: uses and limitationsN B Isada, R F Hume, A Reichler, et al.
American Journal of Human Genetics|October 1, 1996
Prenatal detection of chromosome aneuploidies in uncultured chorionic villus samples by FISHT Bryndorf, B Christensen, M Vad, et al.
Pageof 26

Showing results (201-210 of 251) with videos related to

Sort By:
Pageof 26
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 3, 2001
Laboratory standards and guidelines for population-based cystic fibrosis carrier screeningW W Grody, G R Cutting, K W Klinger, et al.
Human Molecular Genetics|June 22, 2000
Strong homophilic interactions of the Ig-like domains of polycystin-1, the protein product of an autosomal dominant polycystic kidney disease gene, PKD1O Ibraghimov-Beskrovnaya, N O Bukanov, L C Donohue, et al.
American Journal of Obstetrics and Gynecology|December 1, 1992
Rapid prenatal diagnosis by fluorescent in situ hybridization of chorionic villi: an adjunct to long-term culture and karyotypeM I Evans, K W Klinger, N B Isada, et al.
American Journal of Human Genetics|October 23, 1997
PCR quantitation of fetal cells in maternal blood in normal and aneuploid pregnanciesD W Bianchi, J M Williams, L M Sullivan, et al.
Experimental Cell Research|December 20, 2008
Netrin-4 regulates angiogenic responses and tumor cell growthMariana Nacht, Thia B St Martin, Ann Byrne, et al.
Genomics|April 15, 1997
The NTN2L gene encoding a novel human netrin maps to the autosomal dominant polycystic kidney disease region on chromosome 16p13.3T J Van Raay, S M Foskett, T D Connors, et al.
American Journal of Obstetrics and Gynecology|March 23, 2001
Significant fetal-maternal hemorrhage after termination of pregnancy: implications for development of fetal cell microchimerismD W Bianchi, A Farina, W Weber, et al.
Genomics|January 15, 1997
The cloning of a human ABC gene (ABC3) mapping to chromosome 16p13.3T D Connors, T J Van Raay, L R Petry, et al.
Fetal Diagnosis and Therapy|November 1, 1994
Fluorescent in situ hybridization and second-trimester sonographic anomalies: uses and limitationsN B Isada, R F Hume, A Reichler, et al.
American Journal of Human Genetics|October 1, 1996
Prenatal detection of chromosome aneuploidies in uncultured chorionic villus samples by FISHT Bryndorf, B Christensen, M Vad, et al.
Pageof 26