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Nerine Gregersen

Showing results (1-10 of 13) with videos related to

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Clinical Dysmorphology|December 1, 2005
Facial asymmetry with colon atresiaNerine Gregersen
American Journal of Medical Genetics. Part A|August 19, 2004
Costello syndrome with growth hormone deficiency and hypoglycemia: a new report and review of the endocrine associationsNerine Gregersen, Denis Viljoen
Pharmacogenomics|June 4, 2011
Novel CYP2C9 and VKORC1 gene variants associated with warfarin dosage variability in the South African black populationCathrine Mitchell, Nerine Gregersen, Amanda Krause
Journal of Community Genetics|July 12, 2013
The Greater Sekhukhune-CAPABILITY outreach projectNerine Gregersen, Julie Lampret, Tony Lane, et al.
Case Reports in Genetics|July 11, 2013
Delineation of 2q32q35 deletion phenotypes: two apparent "proximal" and "distal" syndromesAdrian Mc Cormack, Juliet Taylor, Nerine Gregersen, et al.
Case Reports in Genetics|August 13, 2015
12q14 Microdeletions: Additional Case Series with Confirmation of a Macrocephaly RegionAdrian Mc Cormack, Cynthia Sharpe, Nerine Gregersen, et al.
Molecular Medicine Reports|March 26, 2013
Developmental delay referrals and the roles of Fragile X testing and molecular karyotyping: a New Zealand perspectiveElaine Doherty, Rachel O'Connor, Anna Zhang, et al.
Journal of Human Genetics|February 26, 2025
Germline mosaicism in TCF20-associated neurodevelopmental disorders: a case study and literature reviewJessie Poquérusse, Whitney Whitford, Juliet Taylor, et al.
Journal of Human Genetics|December 17, 2025
Monoallelic and biallelic RNU4-2 variants in neurodevelopmental disordersYukina Hayashi, Kenta Kajiwara, Seiji Mizuno, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 8, 2017
A craniosynostosis massively parallel sequencing panel study in 309 Australian and New Zealand patients: findings and recommendationsEric Lee, Trang Le, Ying Zhu, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Clinical Dysmorphology|December 1, 2005
Facial asymmetry with colon atresiaNerine Gregersen
American Journal of Medical Genetics. Part A|August 19, 2004
Costello syndrome with growth hormone deficiency and hypoglycemia: a new report and review of the endocrine associationsNerine Gregersen, Denis Viljoen
Pharmacogenomics|June 4, 2011
Novel CYP2C9 and VKORC1 gene variants associated with warfarin dosage variability in the South African black populationCathrine Mitchell, Nerine Gregersen, Amanda Krause
Journal of Community Genetics|July 12, 2013
The Greater Sekhukhune-CAPABILITY outreach projectNerine Gregersen, Julie Lampret, Tony Lane, et al.
Case Reports in Genetics|July 11, 2013
Delineation of 2q32q35 deletion phenotypes: two apparent "proximal" and "distal" syndromesAdrian Mc Cormack, Juliet Taylor, Nerine Gregersen, et al.
Case Reports in Genetics|August 13, 2015
12q14 Microdeletions: Additional Case Series with Confirmation of a Macrocephaly RegionAdrian Mc Cormack, Cynthia Sharpe, Nerine Gregersen, et al.
Molecular Medicine Reports|March 26, 2013
Developmental delay referrals and the roles of Fragile X testing and molecular karyotyping: a New Zealand perspectiveElaine Doherty, Rachel O'Connor, Anna Zhang, et al.
Journal of Human Genetics|February 26, 2025
Germline mosaicism in TCF20-associated neurodevelopmental disorders: a case study and literature reviewJessie Poquérusse, Whitney Whitford, Juliet Taylor, et al.
Journal of Human Genetics|December 17, 2025
Monoallelic and biallelic RNU4-2 variants in neurodevelopmental disordersYukina Hayashi, Kenta Kajiwara, Seiji Mizuno, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 8, 2017
A craniosynostosis massively parallel sequencing panel study in 309 Australian and New Zealand patients: findings and recommendationsEric Lee, Trang Le, Ying Zhu, et al.
Pageof 2