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Regina Regan

Showing results (1-10 of 23) with videos related to

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Plos One|November 29, 2012
HGDP and HapMap analysis by Ancestry Mapper reveals local and global population relationshipsTiago R Magalhães, Jillian P Casey, Judith Conroy, et al.
American Journal of Medical Genetics. Part A|October 25, 2016
Bicoronal and metopic craniosynostosis in association with a de novo unbalanced t(2;7) chromosomal translocationJames J O'Byrne, Helen Ryan, Dylan J Murray, et al.
American Journal of Medical Genetics. Part A|August 16, 2014
A chromosomal 5q31.1 gain involving PITX1 causes Liebenberg syndromeDeirdre Máire Seoighe, Veselina Gadancheva, Regina Regan, et al.
Genomic Medicine|October 17, 2008
Diagnosing idiopathic learning disability: a cost-effectiveness analysis of microarray technology in the National Health Service of the United KingdomSarah Wordsworth, James Buchanan, Regina Regan, et al.
Molecular Genetics and Metabolism|May 22, 2012
Identification of a mutation in LARS as a novel cause of infantile hepatopathyJillian P Casey, Paul McGettigan, Niamh Lynam-Lennon, et al.
Plos One|June 23, 2011
Genomic imbalances are confined to non-proliferating cells in paediatric patients with acute myeloid leukaemia and a normal or incomplete karyotypeErica Ballabio, Regina Regan, Elisa Garimberti, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 11, 2006
Screening of subtelomeric rearrangements in autistic disorder: identification of a partial trisomy of 13q34 in a patient bearing a 13q;21p translocationMaria Antonietta Di Bella, Francesco Calì, Gregorio Seidita, et al.
Human Mutation|September 9, 2011
First implication of STRA6 mutations in isolated anophthalmia, microphthalmia, and coloboma: a new dimension to the STRA6 phenotypeJillian Casey, Riki Kawaguchi, Maria Morrissey, et al.
European Journal of Human Genetics : EJHG|January 27, 2011
The 12q14 microdeletion syndrome: six new cases confirming the role of HMGA2 in growthSally Ann Lynch, Nicola Foulds, Ann-Charlotte Thuresson, et al.
Nucleic Acids Research|June 18, 2005
SW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization dataThomas S Price, Regina Regan, Richard Mott, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Plos One|November 29, 2012
HGDP and HapMap analysis by Ancestry Mapper reveals local and global population relationshipsTiago R Magalhães, Jillian P Casey, Judith Conroy, et al.
American Journal of Medical Genetics. Part A|October 25, 2016
Bicoronal and metopic craniosynostosis in association with a de novo unbalanced t(2;7) chromosomal translocationJames J O'Byrne, Helen Ryan, Dylan J Murray, et al.
American Journal of Medical Genetics. Part A|August 16, 2014
A chromosomal 5q31.1 gain involving PITX1 causes Liebenberg syndromeDeirdre Máire Seoighe, Veselina Gadancheva, Regina Regan, et al.
Genomic Medicine|October 17, 2008
Diagnosing idiopathic learning disability: a cost-effectiveness analysis of microarray technology in the National Health Service of the United KingdomSarah Wordsworth, James Buchanan, Regina Regan, et al.
Molecular Genetics and Metabolism|May 22, 2012
Identification of a mutation in LARS as a novel cause of infantile hepatopathyJillian P Casey, Paul McGettigan, Niamh Lynam-Lennon, et al.
Plos One|June 23, 2011
Genomic imbalances are confined to non-proliferating cells in paediatric patients with acute myeloid leukaemia and a normal or incomplete karyotypeErica Ballabio, Regina Regan, Elisa Garimberti, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 11, 2006
Screening of subtelomeric rearrangements in autistic disorder: identification of a partial trisomy of 13q34 in a patient bearing a 13q;21p translocationMaria Antonietta Di Bella, Francesco Calì, Gregorio Seidita, et al.
Human Mutation|September 9, 2011
First implication of STRA6 mutations in isolated anophthalmia, microphthalmia, and coloboma: a new dimension to the STRA6 phenotypeJillian Casey, Riki Kawaguchi, Maria Morrissey, et al.
European Journal of Human Genetics : EJHG|January 27, 2011
The 12q14 microdeletion syndrome: six new cases confirming the role of HMGA2 in growthSally Ann Lynch, Nicola Foulds, Ann-Charlotte Thuresson, et al.
Nucleic Acids Research|June 18, 2005
SW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization dataThomas S Price, Regina Regan, Richard Mott, et al.
Pageof 3