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D Bick

Showing results (31-40 of 48) with videos related to

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American Journal of Medical Genetics|May 1, 1989
Male infant with ichthyosis, Kallmann syndrome, chondrodysplasia punctata, and an Xp chromosome deletionD Bick, C J Curry, J R McGill, et al.
Anaesthesia|November 17, 2009
Epidural analgesia and breastfeeding: a randomised controlled trial of epidural techniques with and without fentanyl and a non-epidural comparison groupM J A Wilson, C MacArthur, G M Cooper, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1989
Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosomeA Ballabio, B Bardoni, R Carrozzo, et al.
ACS Omega|March 22, 2021
Fomite Transmission, Physicochemical Origin of Virus-Surface Interactions, and Disinfection Strategies for Enveloped Viruses with Applications to SARS-CoV-2Nicolas Castaño, Seth C Cordts, Myra Kurosu Jalil, et al.
Psychiatrike = Psychiatriki|November 13, 2016
Maternal screening for early postnatal vulnerabilityV G Vivilaki, V Dafermos, Ev Patelarou, et al.
Genomics|October 1, 1993
The gene for spondyloepiphyseal dysplasia (SEDL) maps to Xp22 between DXS16 and DXS92S Heuertz, M Nelen, A O Wilkie, et al.
The Journal of Reproductive Medicine|June 4, 1998
Screening semen donors for hereditary diseases. The Fairfax cryobank experienceD Bick, E F Fugger, S H Pool, et al.
Journal of Affective Disorders|October 22, 2019
An exploratory parallel-group randomised controlled trial of antenatal Guided Self-Help (plus usual care) versus usual care alone for pregnant women with depression: DAWN trialK Trevillion, E G Ryan, A Pickles, et al.
Clinical Genetics|July 30, 2013
Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypesE Weh, L M Reis, R C Tyler, et al.
Pilot and Feasibility Studies|October 23, 2022
Antenatal preventative pelvic floor muscle exercise intervention led by midwives to reduce postnatal urinary incontinence (APPEAL): protocol for a feasibility and pilot cluster randomised controlled trialD Bick, J Bishop, T Coleman, et al.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics|May 1, 1989
Male infant with ichthyosis, Kallmann syndrome, chondrodysplasia punctata, and an Xp chromosome deletionD Bick, C J Curry, J R McGill, et al.
Anaesthesia|November 17, 2009
Epidural analgesia and breastfeeding: a randomised controlled trial of epidural techniques with and without fentanyl and a non-epidural comparison groupM J A Wilson, C MacArthur, G M Cooper, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1989
Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosomeA Ballabio, B Bardoni, R Carrozzo, et al.
ACS Omega|March 22, 2021
Fomite Transmission, Physicochemical Origin of Virus-Surface Interactions, and Disinfection Strategies for Enveloped Viruses with Applications to SARS-CoV-2Nicolas Castaño, Seth C Cordts, Myra Kurosu Jalil, et al.
Psychiatrike = Psychiatriki|November 13, 2016
Maternal screening for early postnatal vulnerabilityV G Vivilaki, V Dafermos, Ev Patelarou, et al.
Genomics|October 1, 1993
The gene for spondyloepiphyseal dysplasia (SEDL) maps to Xp22 between DXS16 and DXS92S Heuertz, M Nelen, A O Wilkie, et al.
The Journal of Reproductive Medicine|June 4, 1998
Screening semen donors for hereditary diseases. The Fairfax cryobank experienceD Bick, E F Fugger, S H Pool, et al.
Journal of Affective Disorders|October 22, 2019
An exploratory parallel-group randomised controlled trial of antenatal Guided Self-Help (plus usual care) versus usual care alone for pregnant women with depression: DAWN trialK Trevillion, E G Ryan, A Pickles, et al.
Clinical Genetics|July 30, 2013
Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypesE Weh, L M Reis, R C Tyler, et al.
Pilot and Feasibility Studies|October 23, 2022
Antenatal preventative pelvic floor muscle exercise intervention led by midwives to reduce postnatal urinary incontinence (APPEAL): protocol for a feasibility and pilot cluster randomised controlled trialD Bick, J Bishop, T Coleman, et al.
Pageof 5