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G MacKay

Showing results (291-300 of 332) with videos related to

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Diabetes|April 21, 2007
Mutations in ATP-sensitive K+ channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthoodSarah E Flanagan, Ann-Marie Patch, Deborah J G Mackay, et al.
Pediatric Diabetes|April 30, 2025
Clinical Characteristics and Remission Monitoring of 6q24-Related Transient Neonatal DiabetesMichael E McCullough, Lisa R Letourneau-Freiberg, Tiana L Bowden, et al.
Archives of Disease in Childhood|March 20, 2021
Experiences of adolescents living with Silver-Russell syndromeLisa Marie Ballard, Elizabeth Jenkinson, Christopher D Byrne, et al.
Genetics Research|March 5, 2019
Discrepant molecular and clinical diagnoses in Beckwith-Wiedemann and Silver-Russell syndromesDeborah J G Mackay, Jet Bliek, Maria Paola Lombardi, et al.
Journal of Medical Genetics|February 7, 2014
Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genesLouise E Docherty, Faisal I Rezwan, Rebecca L Poole, et al.
Journal of Clinical Nursing|October 21, 2017
Living with an indwelling urethral catheter in a community setting: Exploring triggers for unscheduled community nurse "out-of-hours" visitsWilliam G Mackay, Teresa MacIntosh, Angela Kydd, et al.
Archives of Disease in Childhood|June 30, 2018
Lived experience of Silver-Russell syndrome: implications for management during childhood and into adulthoodLisa Marie Ballard, Elizabeth Jenkinson, Christopher D Byrne, et al.
Philosophical Transactions. Series A, Mathematical, Physical, and Engineering Sciences|April 18, 2018
Control of cell behaviour through nanovibrational stimulation: nanokickingShaun N Robertson, Paul Campsie, Peter G Childs, et al.
European Journal of Human Genetics : EJHG|February 17, 2018
Revisiting Wilms tumour surveillance in Beckwith-Wiedemann syndrome with IC2 methylation loss, replyFrédéric Brioude, Raoul Hennekam, Jet Bliek, et al.
Diabetologia|February 7, 2013
Clinical presentation of 6q24 transient neonatal diabetes mellitus (6q24 TNDM) and genotype-phenotype correlation in an international cohort of patientsL E Docherty, S Kabwama, A Lehmann, et al.
Pageof 34

Showing results (291-300 of 332) with videos related to

Sort By:
Pageof 34
Diabetes|April 21, 2007
Mutations in ATP-sensitive K+ channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthoodSarah E Flanagan, Ann-Marie Patch, Deborah J G Mackay, et al.
Pediatric Diabetes|April 30, 2025
Clinical Characteristics and Remission Monitoring of 6q24-Related Transient Neonatal DiabetesMichael E McCullough, Lisa R Letourneau-Freiberg, Tiana L Bowden, et al.
Archives of Disease in Childhood|March 20, 2021
Experiences of adolescents living with Silver-Russell syndromeLisa Marie Ballard, Elizabeth Jenkinson, Christopher D Byrne, et al.
Genetics Research|March 5, 2019
Discrepant molecular and clinical diagnoses in Beckwith-Wiedemann and Silver-Russell syndromesDeborah J G Mackay, Jet Bliek, Maria Paola Lombardi, et al.
Journal of Medical Genetics|February 7, 2014
Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genesLouise E Docherty, Faisal I Rezwan, Rebecca L Poole, et al.
Journal of Clinical Nursing|October 21, 2017
Living with an indwelling urethral catheter in a community setting: Exploring triggers for unscheduled community nurse "out-of-hours" visitsWilliam G Mackay, Teresa MacIntosh, Angela Kydd, et al.
Archives of Disease in Childhood|June 30, 2018
Lived experience of Silver-Russell syndrome: implications for management during childhood and into adulthoodLisa Marie Ballard, Elizabeth Jenkinson, Christopher D Byrne, et al.
Philosophical Transactions. Series A, Mathematical, Physical, and Engineering Sciences|April 18, 2018
Control of cell behaviour through nanovibrational stimulation: nanokickingShaun N Robertson, Paul Campsie, Peter G Childs, et al.
European Journal of Human Genetics : EJHG|February 17, 2018
Revisiting Wilms tumour surveillance in Beckwith-Wiedemann syndrome with IC2 methylation loss, replyFrédéric Brioude, Raoul Hennekam, Jet Bliek, et al.
Diabetologia|February 7, 2013
Clinical presentation of 6q24 transient neonatal diabetes mellitus (6q24 TNDM) and genotype-phenotype correlation in an international cohort of patientsL E Docherty, S Kabwama, A Lehmann, et al.
Pageof 34