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A Millington-Ward

Showing results (1-10 of 6) with videos related to

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American Journal of Medical Genetics. Supplement|January 1, 1990
Potential gene sequence isolation and regional mapping in human chromosome 21C Brahe, F Tassone, A Millington-Ward, et al.
American Journal of Medical Genetics. Supplement|January 1, 1990
Molecular study of parental origin of extra chromosome 21 in regular and de novo translocation trisomiesC Brahe, F Tassone, A Moscetti, et al.
Cytometry|September 1, 1986
Construction and analysis of an EMBL-3 phage library containing partially digested human chromosome 21-specific DNA inserts (15-20 kb)J W Janssen, J G Collard, A Tulp, et al.
American Journal of Medical Genetics. Supplement|January 1, 1990
Pericentric inversion of chromosome 9: prevalence in 300 Down syndrome families and molecular studies of nondisjunctionA Serra, C Brahe, A Millington-Ward, et al.
Human Genetics|October 1, 1989
Coincident maternal meiotic nondisjunction of chromosomes X and 21 without evidence of autosomal asynapsisR S Ikonen, M Lindlöf, M O Janas, et al.
American Journal of Human Genetics|October 1, 1986
The X chromosome shows less genetic variation at restriction sites than the autosomesM H Hofker, M I Skraastad, A A Bergen, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Supplement|January 1, 1990
Potential gene sequence isolation and regional mapping in human chromosome 21C Brahe, F Tassone, A Millington-Ward, et al.
American Journal of Medical Genetics. Supplement|January 1, 1990
Molecular study of parental origin of extra chromosome 21 in regular and de novo translocation trisomiesC Brahe, F Tassone, A Moscetti, et al.
Cytometry|September 1, 1986
Construction and analysis of an EMBL-3 phage library containing partially digested human chromosome 21-specific DNA inserts (15-20 kb)J W Janssen, J G Collard, A Tulp, et al.
American Journal of Medical Genetics. Supplement|January 1, 1990
Pericentric inversion of chromosome 9: prevalence in 300 Down syndrome families and molecular studies of nondisjunctionA Serra, C Brahe, A Millington-Ward, et al.
Human Genetics|October 1, 1989
Coincident maternal meiotic nondisjunction of chromosomes X and 21 without evidence of autosomal asynapsisR S Ikonen, M Lindlöf, M O Janas, et al.
American Journal of Human Genetics|October 1, 1986
The X chromosome shows less genetic variation at restriction sites than the autosomesM H Hofker, M I Skraastad, A A Bergen, et al.
Pageof 1