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

B Arveiler

Showing results (51-60 of 64) with videos related to

Pageof 7
Sort By:
Human Genetics|December 1, 1989
Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemiaS Guioli, B Arveiler, B Bardoni, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1987
Close linkage of the locus for X chromosome-linked severe combined immunodeficiency to polymorphic DNA markers in Xq11-q13G de Saint Basile, B Arveiler, I Oberlé, et al.
Human Genetics|October 1, 1987
Close linkage of random DNA fragments from Xq 21.3-22 to X-linked agammaglobulinaemia (XLA)S Malcolm, G de Saint Basile, B Arveiler, et al.
Human Molecular Genetics|February 1, 1993
Human olfactory marker protein maps close to tyrosinase and is a candidate gene for Usher syndrome type IK L Evans, J Fantes, C Simpson, et al.
American Journal of Medical Genetics. Part A|June 29, 2010
Rubinstein-Taybi syndrome and Hirschsprung disease in a patient harboring an intragenic deletion of the CREBBP geneB Isidor, G Podevin, C Camby, et al.
Molecular Psychiatry|April 24, 2001
Genomic structure and localisation within a linkage hotspot of Disrupted In Schizophrenia 1, a gene disrupted by a translocation segregating with schizophreniaJ K Millar, S Christie, S Anderson, et al.
Genetic Counseling (Geneva, Switzerland)|July 16, 2008
Tumoral calcinosis due to GALNT3 C.516-2A >T mutation in a black African familyA Laleye, M J Alao, G Gbessi, et al.
Ophthalmic Genetics|September 13, 2022
Foveal hypoplasia in parents of patients with albinismR Lejoyeux, A-S Alonso, J Lafolie, et al.
Clinical Genetics|August 23, 2006
Mosaic maternal uniparental isodisomy for chromosome 7q21-qterM-P Reboul, O Tandonnet, N Biteau, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|May 27, 2021
Management of albinism: French guidelines for diagnosis and careE Moreno-Artero, F Morice-Picard, D Bremond-Gignac, et al.
Pageof 7

Showing results (51-60 of 64) with videos related to

Sort By:
Pageof 7
Human Genetics|December 1, 1989
Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemiaS Guioli, B Arveiler, B Bardoni, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1987
Close linkage of the locus for X chromosome-linked severe combined immunodeficiency to polymorphic DNA markers in Xq11-q13G de Saint Basile, B Arveiler, I Oberlé, et al.
Human Genetics|October 1, 1987
Close linkage of random DNA fragments from Xq 21.3-22 to X-linked agammaglobulinaemia (XLA)S Malcolm, G de Saint Basile, B Arveiler, et al.
Human Molecular Genetics|February 1, 1993
Human olfactory marker protein maps close to tyrosinase and is a candidate gene for Usher syndrome type IK L Evans, J Fantes, C Simpson, et al.
American Journal of Medical Genetics. Part A|June 29, 2010
Rubinstein-Taybi syndrome and Hirschsprung disease in a patient harboring an intragenic deletion of the CREBBP geneB Isidor, G Podevin, C Camby, et al.
Molecular Psychiatry|April 24, 2001
Genomic structure and localisation within a linkage hotspot of Disrupted In Schizophrenia 1, a gene disrupted by a translocation segregating with schizophreniaJ K Millar, S Christie, S Anderson, et al.
Genetic Counseling (Geneva, Switzerland)|July 16, 2008
Tumoral calcinosis due to GALNT3 C.516-2A >T mutation in a black African familyA Laleye, M J Alao, G Gbessi, et al.
Ophthalmic Genetics|September 13, 2022
Foveal hypoplasia in parents of patients with albinismR Lejoyeux, A-S Alonso, J Lafolie, et al.
Clinical Genetics|August 23, 2006
Mosaic maternal uniparental isodisomy for chromosome 7q21-qterM-P Reboul, O Tandonnet, N Biteau, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|May 27, 2021
Management of albinism: French guidelines for diagnosis and careE Moreno-Artero, F Morice-Picard, D Bremond-Gignac, et al.
Pageof 7