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Nicole Parkinson

Showing results (1-10 of 6) with videos related to

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Developmental Dynamics : an Official Publication of the American Association of Anatomists|February 23, 2010
Expression patterns of hormones, signaling molecules, and transcription factors during adenohypophysis development in the chick embryoNicole Parkinson, Michelle M Collins, Lynn Dufresne, et al.
Human Genetics|October 25, 2013
High frequency of copy number variations (CNVs) in the chromosome 11p15 region in patients with Beckwith-Wiedemann syndromeBerivan Baskin, Sanaa Choufani, Yi-An Chen, et al.
European Journal of Human Genetics : EJHG|July 13, 2017
Wilms tumour in Beckwith-Wiedemann Syndrome and loss of methylation at imprinting centre 2: revisiting tumour surveillance guidelinesJack Brzezinski, Cheryl Shuman, Sanaa Choufani, et al.
Lung Cancer (Amsterdam, Netherlands)|April 28, 2026
Asia-Pacific practical consensus in the management of adverse events related to amivantamab-based therapies in non-small cell lung cancerRoss A Soo, Pablo Fernandez-Penas, Molly Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 23, 2012
Novel 9q34.11 gene deletions encompassing combinations of four Mendelian disease genes: STXBP1, SPTAN1, ENG, and TOR1AIan M Campbell, Svetlana A Yatsenko, Patricia Hixson, et al.
NPJ Genomic Medicine|June 2, 2017
Whole Genome Sequencing Expands Diagnostic Utility and Improves Clinical Management in Pediatric MedicineDimitri J Stavropoulos, Daniele Merico, Rebekah Jobling, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Developmental Dynamics : an Official Publication of the American Association of Anatomists|February 23, 2010
Expression patterns of hormones, signaling molecules, and transcription factors during adenohypophysis development in the chick embryoNicole Parkinson, Michelle M Collins, Lynn Dufresne, et al.
Human Genetics|October 25, 2013
High frequency of copy number variations (CNVs) in the chromosome 11p15 region in patients with Beckwith-Wiedemann syndromeBerivan Baskin, Sanaa Choufani, Yi-An Chen, et al.
European Journal of Human Genetics : EJHG|July 13, 2017
Wilms tumour in Beckwith-Wiedemann Syndrome and loss of methylation at imprinting centre 2: revisiting tumour surveillance guidelinesJack Brzezinski, Cheryl Shuman, Sanaa Choufani, et al.
Lung Cancer (Amsterdam, Netherlands)|April 28, 2026
Asia-Pacific practical consensus in the management of adverse events related to amivantamab-based therapies in non-small cell lung cancerRoss A Soo, Pablo Fernandez-Penas, Molly Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 23, 2012
Novel 9q34.11 gene deletions encompassing combinations of four Mendelian disease genes: STXBP1, SPTAN1, ENG, and TOR1AIan M Campbell, Svetlana A Yatsenko, Patricia Hixson, et al.
NPJ Genomic Medicine|June 2, 2017
Whole Genome Sequencing Expands Diagnostic Utility and Improves Clinical Management in Pediatric MedicineDimitri J Stavropoulos, Daniele Merico, Rebekah Jobling, et al.
Pageof 1