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Gillian Turner

Showing results (11-20 of 53) with videos related to

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Bone & Joint Open|July 12, 2021
Should isolated morbid obesity influence the decision to operate in hip and knee arthroplasty?Peter F Crookes, Roslyn S Cassidy, Aleksander Machowicz, et al.
Australian Critical Care : Official Journal of the Confederation of Australian Critical Care Nurses|November 28, 2007
Multicentre study of delirium in ICU patients using a simple screening toolBrigit Roberts, Claire M Rickard, Dorrilyn Rajbhandari, et al.
American Journal of Medical Genetics. Part A|March 26, 2014
The intellectual disabilities evaluation and advice system (IDEAS): outcome of the first 55 casesAlasdair G W Hunter, John M Graham, Giovanni Neri, et al.
BMJ Open|December 16, 2022
Impact of the COVID-19 pandemic on expectant and new parents' experience of pregnancy, childbirth, breast feeding, parental responsiveness and sensitivity, and bonding and attunement in high-income countries: a systematic review of the evidenceAdenike Motunrayo Adesanya, Simon Barrett, Malcolm Moffat, et al.
Human Molecular Genetics|January 13, 2010
Mutations in Cullin 4B result in a human syndrome associated with increased camptothecin-induced topoisomerase I-dependent DNA breaksClaudia Kerzendorfer, Annabel Whibley, Gillian Carpenter, et al.
European Journal of Human Genetics : EJHG|July 9, 2004
1024C> T (R342X) is a recurrent PHF6 mutation also found in the original Börjeson-Forssman-Lehmann syndrome familyKaren M Lower, Göran Solders, Marie-Louise Bondeson, et al.
Human Mutation|March 17, 2006
Novel JARID1C/SMCX mutations in patients with X-linked mental retardationAndreas Tzschach, Steffen Lenzner, Bettina Moser, et al.
European Journal of Human Genetics : EJHG|May 26, 2016
A non-coding variant in the 5' UTR of DLG3 attenuates protein translation to cause non-syndromic intellectual disabilityRaman Kumar, Thuong Ha, Duyen Pham, et al.
BMJ Open|November 22, 2024
Evaluating the effectiveness of the National Health Insurance Subsidy Programme within Kenya's universal health coverage initiative: a study protocolBeryl Maritim, Jacinta Nzinga, Benjamin Tsofa, et al.
European Journal of Human Genetics : EJHG|September 14, 2006
X-linked mental retardation: a comprehensive molecular screen of 47 candidate genes from a 7.4 Mb interval in Xp11Lars Riff Jensen, Steffen Lenzner, Bettina Moser, et al.
Pageof 6

Showing results (11-20 of 53) with videos related to

Sort By:
Pageof 6
Bone & Joint Open|July 12, 2021
Should isolated morbid obesity influence the decision to operate in hip and knee arthroplasty?Peter F Crookes, Roslyn S Cassidy, Aleksander Machowicz, et al.
Australian Critical Care : Official Journal of the Confederation of Australian Critical Care Nurses|November 28, 2007
Multicentre study of delirium in ICU patients using a simple screening toolBrigit Roberts, Claire M Rickard, Dorrilyn Rajbhandari, et al.
American Journal of Medical Genetics. Part A|March 26, 2014
The intellectual disabilities evaluation and advice system (IDEAS): outcome of the first 55 casesAlasdair G W Hunter, John M Graham, Giovanni Neri, et al.
BMJ Open|December 16, 2022
Impact of the COVID-19 pandemic on expectant and new parents' experience of pregnancy, childbirth, breast feeding, parental responsiveness and sensitivity, and bonding and attunement in high-income countries: a systematic review of the evidenceAdenike Motunrayo Adesanya, Simon Barrett, Malcolm Moffat, et al.
Human Molecular Genetics|January 13, 2010
Mutations in Cullin 4B result in a human syndrome associated with increased camptothecin-induced topoisomerase I-dependent DNA breaksClaudia Kerzendorfer, Annabel Whibley, Gillian Carpenter, et al.
European Journal of Human Genetics : EJHG|July 9, 2004
1024C> T (R342X) is a recurrent PHF6 mutation also found in the original Börjeson-Forssman-Lehmann syndrome familyKaren M Lower, Göran Solders, Marie-Louise Bondeson, et al.
Human Mutation|March 17, 2006
Novel JARID1C/SMCX mutations in patients with X-linked mental retardationAndreas Tzschach, Steffen Lenzner, Bettina Moser, et al.
European Journal of Human Genetics : EJHG|May 26, 2016
A non-coding variant in the 5' UTR of DLG3 attenuates protein translation to cause non-syndromic intellectual disabilityRaman Kumar, Thuong Ha, Duyen Pham, et al.
BMJ Open|November 22, 2024
Evaluating the effectiveness of the National Health Insurance Subsidy Programme within Kenya's universal health coverage initiative: a study protocolBeryl Maritim, Jacinta Nzinga, Benjamin Tsofa, et al.
European Journal of Human Genetics : EJHG|September 14, 2006
X-linked mental retardation: a comprehensive molecular screen of 47 candidate genes from a 7.4 Mb interval in Xp11Lars Riff Jensen, Steffen Lenzner, Bettina Moser, et al.
Pageof 6