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

E Sarret

Showing results (11-20 of 19) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 19 results.
American Journal of Medical Genetics|February 13, 2001
Variegated aneuploidy related to premature centromere division (PCD) is expressed in vivo and is a cancer-prone diseaseA Plaja, T Vendrell, D Smeets, et al.
Human Mutation|April 24, 2001
Spectrum of germline RB1 gene mutations in Spanish retinoblastoma patients: Phenotypic and molecular epidemiological implicationsJ Alonso, P García-Miguel, J Abelairas, et al.
Anales De Pediatria (Barcelona, Spain : 2003)|March 12, 2003
[Bone age delay and hypoplastic thumbs in a five year-old boy]P Soler Palacín, D Panadès Mas, R Porcel Rubio, et al.
Journal of Medical Genetics|October 4, 2002
Familial expansile osteolysis in a large Spanish kindred resulting from an insertion mutation in the TNFRSF11A geneL Palenzuela, C Vives-Bauza, I Fernández-Cadenas, et al.
Annales De Genetique|January 1, 1994
Terminal deletion of 6p: report of a new caseA Plaja, R Vidal, D Soriano, et al.
Annales De Genetique|January 1, 1985
A case of male pseudohermaphroditism with normal androgen receptor binding and 47,XYY karyotypeJ M Bosch-Banyeras, L Audi, E Sarret, et al.
Human Mutation|April 24, 2001
Five novel single nucleotide polymorphisms of the RB1 gene (g.5625T>C, g.70169T>G, g.76875A>T, g.78026delA, and g.150072T>C) in retinoblastoma patientsJ Alonso, C Moreno, A López, et al.
Journal of Medical Genetics|October 3, 1999
Molecular characterisation of partial chromosome 21 aneuploidies by fluorescent PCRR Valero, G Marfany, R Gil-Benso, et al.
Acta Obstetrica Y Ginecologica Hispano-Lusitana|April 1, 1977
[Considerations on the genetic study of amniotic fluid cells]M Muxí, J Prats, J Xercavins, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
American Journal of Medical Genetics|February 13, 2001
Variegated aneuploidy related to premature centromere division (PCD) is expressed in vivo and is a cancer-prone diseaseA Plaja, T Vendrell, D Smeets, et al.
Human Mutation|April 24, 2001
Spectrum of germline RB1 gene mutations in Spanish retinoblastoma patients: Phenotypic and molecular epidemiological implicationsJ Alonso, P García-Miguel, J Abelairas, et al.
Anales De Pediatria (Barcelona, Spain : 2003)|March 12, 2003
[Bone age delay and hypoplastic thumbs in a five year-old boy]P Soler Palacín, D Panadès Mas, R Porcel Rubio, et al.
Journal of Medical Genetics|October 4, 2002
Familial expansile osteolysis in a large Spanish kindred resulting from an insertion mutation in the TNFRSF11A geneL Palenzuela, C Vives-Bauza, I Fernández-Cadenas, et al.
Annales De Genetique|January 1, 1994
Terminal deletion of 6p: report of a new caseA Plaja, R Vidal, D Soriano, et al.
Annales De Genetique|January 1, 1985
A case of male pseudohermaphroditism with normal androgen receptor binding and 47,XYY karyotypeJ M Bosch-Banyeras, L Audi, E Sarret, et al.
Human Mutation|April 24, 2001
Five novel single nucleotide polymorphisms of the RB1 gene (g.5625T>C, g.70169T>G, g.76875A>T, g.78026delA, and g.150072T>C) in retinoblastoma patientsJ Alonso, C Moreno, A López, et al.
Journal of Medical Genetics|October 3, 1999
Molecular characterisation of partial chromosome 21 aneuploidies by fluorescent PCRR Valero, G Marfany, R Gil-Benso, et al.
Acta Obstetrica Y Ginecologica Hispano-Lusitana|April 1, 1977
[Considerations on the genetic study of amniotic fluid cells]M Muxí, J Prats, J Xercavins, et al.
Pageof 2