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

Human genetics

Showing results (1231-1240 of 9,569) with videos related to

Pageof 957
Sort By:
Human Genetics|March 25, 2019
Natural models for retinitis pigmentosa: progressive retinal atrophy in dog breedsMorgane Bunel, Gilles Chaudieu, Christian Hamel, et al.
Human Genetics|April 5, 1979
An automatic system for chromosomal analysis applied to prenatal diagnosisC Léonard, P Saint-Jean, D Schoëvaërt, et al.
Human Genetics|March 1, 1986
Analysis of spreading of inactivation in eight X autosome translocations utilizing the high resolution RBG techniqueE A Keitges, C G Palmer
Human Genetics|March 1, 1986
Oncogenes and the mammalian X chromosomeH Hameister, S Adolph
Human Genetics|March 1, 1986
Mental impairment in Martin-Bell syndrome is probably determined by interaction of several genes: simple explanation of phenotypic differences between unaffected and affected males with the same X chromosomeP Steinbach
Human Genetics|March 1, 1986
Prophase pairing in a mosaic 18p-;iso 18q human female foetus studied by surface spreadingR M Speed
Human Genetics|January 1, 1985
A cytogenetic study of a population of retarded females with special reference to the fragile (X) syndromeM Mayer, M A Abruzzo, P A Jacobs, et al.
Human Genetics|January 1, 1985
A new alpha 1-antitrypsin allele PI Poki: isoelectric focusing with immobilized pH gradients as a tool for identification for PI variantsI Yuasa, K Okada
Human Genetics|January 1, 1985
The infantile form of sialidosis type II associated with congenital adrenal hyperplasia: possible linkage between HLA and the neuraminidase deficiency geneT Oohira, N Nagata, I Akaboshi, et al.
Human Genetics|July 4, 2012
Novel neurodevelopmental information revealed in amniotic fluid supernatant transcripts from fetuses with trisomies 18 and 21Lisa Hui, Donna K Slonim, Heather C Wick, et al.
Pageof 957

Showing results (1231-1240 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|March 25, 2019
Natural models for retinitis pigmentosa: progressive retinal atrophy in dog breedsMorgane Bunel, Gilles Chaudieu, Christian Hamel, et al.
Human Genetics|April 5, 1979
An automatic system for chromosomal analysis applied to prenatal diagnosisC Léonard, P Saint-Jean, D Schoëvaërt, et al.
Human Genetics|March 1, 1986
Analysis of spreading of inactivation in eight X autosome translocations utilizing the high resolution RBG techniqueE A Keitges, C G Palmer
Human Genetics|March 1, 1986
Oncogenes and the mammalian X chromosomeH Hameister, S Adolph
Human Genetics|March 1, 1986
Mental impairment in Martin-Bell syndrome is probably determined by interaction of several genes: simple explanation of phenotypic differences between unaffected and affected males with the same X chromosomeP Steinbach
Human Genetics|March 1, 1986
Prophase pairing in a mosaic 18p-;iso 18q human female foetus studied by surface spreadingR M Speed
Human Genetics|January 1, 1985
A cytogenetic study of a population of retarded females with special reference to the fragile (X) syndromeM Mayer, M A Abruzzo, P A Jacobs, et al.
Human Genetics|January 1, 1985
A new alpha 1-antitrypsin allele PI Poki: isoelectric focusing with immobilized pH gradients as a tool for identification for PI variantsI Yuasa, K Okada
Human Genetics|January 1, 1985
The infantile form of sialidosis type II associated with congenital adrenal hyperplasia: possible linkage between HLA and the neuraminidase deficiency geneT Oohira, N Nagata, I Akaboshi, et al.
Human Genetics|July 4, 2012
Novel neurodevelopmental information revealed in amniotic fluid supernatant transcripts from fetuses with trisomies 18 and 21Lisa Hui, Donna K Slonim, Heather C Wick, et al.
Pageof 957