Search research articles
Contact Us
Filters
Showing results (71-80 of 75) with videos related to
Page
of 8
Sort By:
You have reached the last page of results.
This site can display upto 75 results.
Nature Genetics
|
May 1, 1997
Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome
E Rao, B Weiss, M Fukami, et al.
Genome Research
|
June 16, 2000
Comparative genome sequence analysis of the Bpa/Str region in mouse and Man
A M Mallon, M Platzer, R Bate, et al.
Nature
|
June 1, 2000
The DNA sequence of human chromosome 21
M Hattori, A Fujiyama, T D Taylor, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
August 21, 2022
Comprehensive cancer predisposition testing within the prospective MASTER trial identifies hereditary cancer patients and supports treatment decisions for rare cancers
A Jahn, A Rump, T J Widmann, et al.
Nature
|
March 10, 2001
Initial sequencing and analysis of the human genome
E S Lander, L M Linton, B Birren, et al.
Page
of 8
Search research articles
Search
Showing results (71-80 of 75) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 75 results.
Nature Genetics
|
May 1, 1997
Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome
E Rao, B Weiss, M Fukami, et al.
Genome Research
|
June 16, 2000
Comparative genome sequence analysis of the Bpa/Str region in mouse and Man
A M Mallon, M Platzer, R Bate, et al.
Nature
|
June 1, 2000
The DNA sequence of human chromosome 21
M Hattori, A Fujiyama, T D Taylor, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
August 21, 2022
Comprehensive cancer predisposition testing within the prospective MASTER trial identifies hereditary cancer patients and supports treatment decisions for rare cancers
A Jahn, A Rump, T J Widmann, et al.
Nature
|
March 10, 2001
Initial sequencing and analysis of the human genome
E S Lander, L M Linton, B Birren, et al.
Page
of 8