Search research articles
Contact Us
Filters
Showing results (461-470 of 471) with videos related to
Page
of 48
Sort By:
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 17, 2011
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities
Erin B Kaminsky, Vineith Kaul, Justin Paschall, et al.
Nature
|
May 10, 2002
Complete genome sequence of the model actinomycete Streptomyces coelicolor A3(2)
S D Bentley, K F Chater, A-M Cerdeño-Tárraga, et al.
American Journal of Human Genetics
|
November 9, 2010
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia
Daniel Moreno-De-Luca, , Jennifer G Mulle, et al.
Journal of Clinical Immunology
|
July 9, 2020
Neuroinflammatory Disease as an Isolated Manifestation of Hemophagocytic Lymphohistiocytosis
Annaliesse Blincoe, Maximilian Heeg, Patrick K Campbell, et al.
Plos Genetics
|
March 14, 2012
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci
Eimear E Kenny, Itsik Pe'er, Amir Karban, et al.
Nature
|
February 23, 2002
The genome sequence of Schizosaccharomyces pombe
V Wood, R Gwilliam, M-A Rajandream, et al.
Molecular Psychiatry
|
February 5, 2020
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
Isabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, et al.
Space Science Reviews
|
March 19, 2019
SEIS: Insight's Seismic Experiment for Internal Structure of Mars
P Lognonné, W B Banerdt, D Giardini, et al.
Nature
|
March 17, 2006
The finished DNA sequence of human chromosome 12
Steven E Scherer, Donna M Muzny, Christian J Buhay, et al.
Science (New York, N.Y.)
|
April 25, 2009
The genome sequence of taurine cattle: a window to ruminant biology and evolution
, Christine G Elsik, Ross L Tellam, et al.
Page
of 48
Search research articles
Search
Showing results (461-470 of 471) with videos related to
Sort By:
Page
of 48
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 17, 2011
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities
Erin B Kaminsky, Vineith Kaul, Justin Paschall, et al.
Nature
|
May 10, 2002
Complete genome sequence of the model actinomycete Streptomyces coelicolor A3(2)
S D Bentley, K F Chater, A-M Cerdeño-Tárraga, et al.
American Journal of Human Genetics
|
November 9, 2010
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia
Daniel Moreno-De-Luca, , Jennifer G Mulle, et al.
Journal of Clinical Immunology
|
July 9, 2020
Neuroinflammatory Disease as an Isolated Manifestation of Hemophagocytic Lymphohistiocytosis
Annaliesse Blincoe, Maximilian Heeg, Patrick K Campbell, et al.
Plos Genetics
|
March 14, 2012
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci
Eimear E Kenny, Itsik Pe'er, Amir Karban, et al.
Nature
|
February 23, 2002
The genome sequence of Schizosaccharomyces pombe
V Wood, R Gwilliam, M-A Rajandream, et al.
Molecular Psychiatry
|
February 5, 2020
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
Isabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, et al.
Space Science Reviews
|
March 19, 2019
SEIS: Insight's Seismic Experiment for Internal Structure of Mars
P Lognonné, W B Banerdt, D Giardini, et al.
Nature
|
March 17, 2006
The finished DNA sequence of human chromosome 12
Steven E Scherer, Donna M Muzny, Christian J Buhay, et al.
Science (New York, N.Y.)
|
April 25, 2009
The genome sequence of taurine cattle: a window to ruminant biology and evolution
, Christine G Elsik, Ross L Tellam, et al.
Page
of 48