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

P C Patsalis

Showing results (1-10 of 29) with videos related to

Pageof 3
Sort By:
Genetic Counseling (Geneva, Switzerland)|May 23, 2007
Complex chromosomal rearrangementsP C Patsalis
Nucleic Acids Research|December 22, 1999
Measurement of locus copy number by hybridisation with amplifiable probesJ A Armour, C Sismani, P C Patsalis, et al.
Human Biology|May 26, 1998
Variation in the number of FMR1 microsatellite repeats in three subgroups of the Hellenic populationM Syrrou, P C Patsalis, I Georgiou, et al.
International Journal of Andrology|May 29, 2002
A nation-based population screening for azoospermia factor deletions in Greek-Cypriot patients with severe spermatogenic failure and normal fertile controls, using a specific study and experimental designA Ioulianos, C Sismani, N Fourouclas, et al.
European Journal of Human Genetics : EJHG|July 21, 2001
Screening for subtelomeric chromosome abnormalities in children with idiopathic mental retardation using multiprobe telomeric FISH and the new MAPH telomeric assayC Sismani, J A Armour, J Flint, et al.
American Journal of Medical Genetics|May 20, 1999
Fragile X premutations and (TA)n estrogen receptor polymorphism in women with ovarian dysfunctionM Syrrou, I Georgiou, P C Patsalis, et al.
Genetic Epidemiology|April 2, 1998
FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic populationM Syrrou, I Georgiou, M Grigoriadou, et al.
Human Genetics|January 28, 1999
Loss of heterozygosity in polycystic kidney disease with a missense mutation in the repeated region of PKD1M Koptides, R Constantinides, G Kyriakides, et al.
American Journal of Medical Genetics|July 12, 1996
Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and CyprusM Syrrou, P C Patsalis, I Georgiou, et al.
Biochimica Et Biophysica Acta|April 20, 2001
ZNF232: structure and expression analysis of a novel human C(2)H(2) zinc finger gene, member of the SCAN/LeR domain subfamilyL A Mavrogiannis, A Argyrokastritis, N Tzitzikas, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
Genetic Counseling (Geneva, Switzerland)|May 23, 2007
Complex chromosomal rearrangementsP C Patsalis
Nucleic Acids Research|December 22, 1999
Measurement of locus copy number by hybridisation with amplifiable probesJ A Armour, C Sismani, P C Patsalis, et al.
Human Biology|May 26, 1998
Variation in the number of FMR1 microsatellite repeats in three subgroups of the Hellenic populationM Syrrou, P C Patsalis, I Georgiou, et al.
International Journal of Andrology|May 29, 2002
A nation-based population screening for azoospermia factor deletions in Greek-Cypriot patients with severe spermatogenic failure and normal fertile controls, using a specific study and experimental designA Ioulianos, C Sismani, N Fourouclas, et al.
European Journal of Human Genetics : EJHG|July 21, 2001
Screening for subtelomeric chromosome abnormalities in children with idiopathic mental retardation using multiprobe telomeric FISH and the new MAPH telomeric assayC Sismani, J A Armour, J Flint, et al.
American Journal of Medical Genetics|May 20, 1999
Fragile X premutations and (TA)n estrogen receptor polymorphism in women with ovarian dysfunctionM Syrrou, I Georgiou, P C Patsalis, et al.
Genetic Epidemiology|April 2, 1998
FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic populationM Syrrou, I Georgiou, M Grigoriadou, et al.
Human Genetics|January 28, 1999
Loss of heterozygosity in polycystic kidney disease with a missense mutation in the repeated region of PKD1M Koptides, R Constantinides, G Kyriakides, et al.
American Journal of Medical Genetics|July 12, 1996
Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and CyprusM Syrrou, P C Patsalis, I Georgiou, et al.
Biochimica Et Biophysica Acta|April 20, 2001
ZNF232: structure and expression analysis of a novel human C(2)H(2) zinc finger gene, member of the SCAN/LeR domain subfamilyL A Mavrogiannis, A Argyrokastritis, N Tzitzikas, et al.
Pageof 3