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Showing results (71-80 of 76) with videos related to

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Clinical Genetics|July 12, 2017
Clinical experience with a single-nucleotide polymorphism-based non-invasive prenatal test for five clinically significant microdeletionsK Martin, S Iyengar, A Kalyan, et al.
Cancer|January 1, 1993
Steroid hormone receptor immunohistochemistry and amplification of c-myc protooncogene. Relationship to disease-free survival in breast cancerL P Pertschuk, J G Feldman, D S Kim, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 18, 2018
Fetal fraction-based risk algorithm for non-invasive prenatal testing: screening for trisomies 13 and 18 and triploidy in women with low cell-free fetal DNAT McKanna, A Ryan, S Krinshpun, et al.
HIV Medicine|July 17, 2020
Polypharmacy and potential drug-drug interactions for people with HIV in the UK from the Climate-HIV databaseC Okoli, A Schwenk, M Radford, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|September 24, 2015
Clinical experience with single-nucleotide polymorphism-based non-invasive prenatal screening for 22q11.2 deletion syndromeS J Gross, M Stosic, D M McDonald-McGinn, et al.
Prenatal Diagnosis|March 1, 2000
Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlationsR Wallerstein, M T Yu, R L Neu, et al.
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Showing results (71-80 of 76) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 76 results.
Clinical Genetics|July 12, 2017
Clinical experience with a single-nucleotide polymorphism-based non-invasive prenatal test for five clinically significant microdeletionsK Martin, S Iyengar, A Kalyan, et al.
Cancer|January 1, 1993
Steroid hormone receptor immunohistochemistry and amplification of c-myc protooncogene. Relationship to disease-free survival in breast cancerL P Pertschuk, J G Feldman, D S Kim, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 18, 2018
Fetal fraction-based risk algorithm for non-invasive prenatal testing: screening for trisomies 13 and 18 and triploidy in women with low cell-free fetal DNAT McKanna, A Ryan, S Krinshpun, et al.
HIV Medicine|July 17, 2020
Polypharmacy and potential drug-drug interactions for people with HIV in the UK from the Climate-HIV databaseC Okoli, A Schwenk, M Radford, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|September 24, 2015
Clinical experience with single-nucleotide polymorphism-based non-invasive prenatal screening for 22q11.2 deletion syndromeS J Gross, M Stosic, D M McDonald-McGinn, et al.
Prenatal Diagnosis|March 1, 2000
Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlationsR Wallerstein, M T Yu, R L Neu, et al.
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