Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Rebecca L Poole

Showing results (1-10 of 18) with videos related to

Pageof 2
Sort By:
Methods in Molecular Biology (Clifton, N.J.)|February 22, 2008
The TAIR databaseRebecca L Poole
American Journal of Medical Genetics. Part A|July 17, 2010
Investigation of 90 patients referred for molecular cytogenetic analysis using aCGH uncovers previously unsuspected anomalies of imprintingRebecca L Poole, Emma Baple, John A Crolla, et al.
The American Surgeon|January 9, 2015
Postpartum transabdominal laparoscopic adrenalectomy for pheochromocytoma presenting with abruption and hypertensive emergencyKatherine I Warner, Rebecca L Poole-Ward, Ashley Martinez, et al.
European Journal of Human Genetics : EJHG|July 10, 2014
Very small deletions within the NESP55 gene in pseudohypoparathyroidism type 1bFaisal I Rezwan, Rebecca L Poole, Trine Prescott, et al.
Clinical Dysmorphology|March 6, 2023
The PHF21A neurodevelopmental disorder: an evaluation of clinical data from 13 patientsRebecca L Poole, Emilia K Bijlsma, Gunnar Houge, et al.
European Journal of Human Genetics : EJHG|January 6, 2011
An atypical case of hypomethylation at multiple imprinted lociEmma L Baple, Rebecca L Poole, Sahar Mansour, et al.
European Journal of Human Genetics : EJHG|August 25, 2011
Beckwith-Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1Rebecca L Poole, Donald J Leith, Louise E Docherty, et al.
Clinical Epigenetics|April 29, 2015
A statistical method for single sample analysis of HumanMethylation450 array data: genome-wide methylation analysis of patients with imprinting disordersFaisal I Rezwan, Louise E Docherty, Rebecca L Poole, et al.
BMC Genomics|October 14, 2008
Analysis of wheat SAGE tags reveals evidence for widespread antisense transcriptionRebecca L Poole, Gary L A Barker, Kay Werner, et al.
European Journal of Medical Genetics|January 13, 2023
Expanding the neurodevelopmental phenotype associated with HK1 de novo heterozygous missense variantsRebecca L Poole, Mihaly Badonyi, Alison Cozens, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Methods in Molecular Biology (Clifton, N.J.)|February 22, 2008
The TAIR databaseRebecca L Poole
American Journal of Medical Genetics. Part A|July 17, 2010
Investigation of 90 patients referred for molecular cytogenetic analysis using aCGH uncovers previously unsuspected anomalies of imprintingRebecca L Poole, Emma Baple, John A Crolla, et al.
The American Surgeon|January 9, 2015
Postpartum transabdominal laparoscopic adrenalectomy for pheochromocytoma presenting with abruption and hypertensive emergencyKatherine I Warner, Rebecca L Poole-Ward, Ashley Martinez, et al.
European Journal of Human Genetics : EJHG|July 10, 2014
Very small deletions within the NESP55 gene in pseudohypoparathyroidism type 1bFaisal I Rezwan, Rebecca L Poole, Trine Prescott, et al.
Clinical Dysmorphology|March 6, 2023
The PHF21A neurodevelopmental disorder: an evaluation of clinical data from 13 patientsRebecca L Poole, Emilia K Bijlsma, Gunnar Houge, et al.
European Journal of Human Genetics : EJHG|January 6, 2011
An atypical case of hypomethylation at multiple imprinted lociEmma L Baple, Rebecca L Poole, Sahar Mansour, et al.
European Journal of Human Genetics : EJHG|August 25, 2011
Beckwith-Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1Rebecca L Poole, Donald J Leith, Louise E Docherty, et al.
Clinical Epigenetics|April 29, 2015
A statistical method for single sample analysis of HumanMethylation450 array data: genome-wide methylation analysis of patients with imprinting disordersFaisal I Rezwan, Louise E Docherty, Rebecca L Poole, et al.
BMC Genomics|October 14, 2008
Analysis of wheat SAGE tags reveals evidence for widespread antisense transcriptionRebecca L Poole, Gary L A Barker, Kay Werner, et al.
European Journal of Medical Genetics|January 13, 2023
Expanding the neurodevelopmental phenotype associated with HK1 de novo heterozygous missense variantsRebecca L Poole, Mihaly Badonyi, Alison Cozens, et al.
Pageof 2