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 Kiss

Showing results (11-20 of 188) with videos related to

Pageof 19
Sort By:
Orvosi Hetilap|June 4, 1972
[Sex chromosome abnormalities in childhood. I. XXY and XXY mosaic]P Kiss, M Osztovics
Acta Paediatrica Academiae Scientiarum Hungaricae|January 1, 1978
Mild variant of maple syrup urine diseaseJ Kovács, P Kiss
Acta Paediatrica Academiae Scientiarum Hungaricae|January 1, 1982
Trisomy 5q15-q31 due to maternal insertion, ins (6; 5) (q21; q15q31)M Osztovics, P Kiss
Journal of Medical Genetics|December 1, 1989
Association of 13q deletion and Hirschsprung's diseaseP Kiss, M Osztovics
Zeitschrift Fur Die Gesamte Innere Medizin Und Ihre Grenzgebiete|June 1, 1981
[Cytogenetic investigations in 817 dysmorphic babies]P Kiss, M Osztovics
Pediatric Dermatology|September 1, 1990
Autosomal recessive inheritance of hypohidrotic ectodermal dysplasiaP Kiss, E Török
Annales De Genetique|January 1, 1993
10p monosomy, a phenotypic variantP Kiss, M Osztovics
Acta Paediatrica Academiae Scientiarum Hungaricae|January 1, 1982
Down syndrome: correspondence of clinical diagnosis and karyotypeM Osztovics, P Kiss
Acta Paediatrica Hungarica|January 1, 1987
Partial deletion of short arm of chromosome 8P Kiss, M Osztovics
Clinical Genetics|November 1, 1990
Familial translocation, t(2;5)(p23;q31) follow-up after 15 yearsP Kiss, M Osztovics
Pageof 19

Showing results (11-20 of 188) with videos related to

Sort By:
Pageof 19
Orvosi Hetilap|June 4, 1972
[Sex chromosome abnormalities in childhood. I. XXY and XXY mosaic]P Kiss, M Osztovics
Acta Paediatrica Academiae Scientiarum Hungaricae|January 1, 1978
Mild variant of maple syrup urine diseaseJ Kovács, P Kiss
Acta Paediatrica Academiae Scientiarum Hungaricae|January 1, 1982
Trisomy 5q15-q31 due to maternal insertion, ins (6; 5) (q21; q15q31)M Osztovics, P Kiss
Journal of Medical Genetics|December 1, 1989
Association of 13q deletion and Hirschsprung's diseaseP Kiss, M Osztovics
Zeitschrift Fur Die Gesamte Innere Medizin Und Ihre Grenzgebiete|June 1, 1981
[Cytogenetic investigations in 817 dysmorphic babies]P Kiss, M Osztovics
Pediatric Dermatology|September 1, 1990
Autosomal recessive inheritance of hypohidrotic ectodermal dysplasiaP Kiss, E Török
Annales De Genetique|January 1, 1993
10p monosomy, a phenotypic variantP Kiss, M Osztovics
Acta Paediatrica Academiae Scientiarum Hungaricae|January 1, 1982
Down syndrome: correspondence of clinical diagnosis and karyotypeM Osztovics, P Kiss
Acta Paediatrica Hungarica|January 1, 1987
Partial deletion of short arm of chromosome 8P Kiss, M Osztovics
Clinical Genetics|November 1, 1990
Familial translocation, t(2;5)(p23;q31) follow-up after 15 yearsP Kiss, M Osztovics
Pageof 19