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BMC Medical Informatics and Decision Making
|
May 20, 2009
Different patient case mix by applying the 2003 SCCM/ESICM/ACCP/ATS/SIS sepsis definitions instead of the 1992 ACCP/SCCM sepsis definitions in surgical patients: a retrospective observational study
Manfred Weiss, Markus Huber-Lang, Michael Taenzer, et al.
Genomics
|
April 1, 1992
Chromosome mapping of the rod photoreceptor cGMP phosphodiesterase beta-subunit gene in mouse and human: tight linkage to the Huntington disease region (4p16.3)
M R Altherr, J J Wasmuth, M F Seldin, et al.
Scientific Reports
|
October 9, 2025
Using an electronic frailty index and patient reported outcomes to predict sarcopenia risk
Cody A Altherr, Xiao Luo, Haoran Ding, et al.
Genomics
|
May 20, 1995
Mapping of the gene for the Mel1a-melatonin receptor to human chromosome 4 (MTNR1A) and mouse chromosome 8 (Mtnr1a)
S A Slaugenhaupt, A L Roca, C B Liebert, et al.
American Journal of Medical Genetics
|
November 1, 1992
Molecular detection of a 4p deletion using PCR-based polymorphisms: a technique for the rapid detection of the Wolf-Hirschhorn syndrome
M R Altherr, J F Gusella, J J Wasmuth, et al.
Nutrition Today
|
October 18, 2021
Dietary Nitrate Supplementation and Exercise-Related Performance
Marissa N Baranauskas, Andrew R Coggan, Allison H Gruber, et al.
Genomics
|
December 1, 1991
A gene encoding a fibroblast growth factor receptor isolated from the Huntington disease gene region of human chromosome 4
L M Thompson, S Plummer, M Schalling, et al.
Human Molecular Genetics
|
October 1, 1996
The evolutionary distribution and structural organization of the homeobox-containing repeat D4Z4 indicates a functional role for the ancestral copy in the FSHD region
S T Winokur, U Bengtsson, J C Vargas, et al.
American Journal of Medical Genetics
|
March 17, 2001
First known microdeletion within the Wolf-Hirschhorn syndrome critical region refines genotype-phenotype correlation
A Rauch, S Schellmoser, C Kraus, et al.
Molecular and Cellular Probes
|
December 1, 1992
Assay by polymerase chain reaction (PCR) of multi-allele polymorphisms in the Huntington's disease region of chromosome 4
B A Allitto, A I McClatchey, G Barnes, et al.
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of 13
Search research articles
Search
Showing results (61-70 of 127) with videos related to
Sort By:
Page
of 13
BMC Medical Informatics and Decision Making
|
May 20, 2009
Different patient case mix by applying the 2003 SCCM/ESICM/ACCP/ATS/SIS sepsis definitions instead of the 1992 ACCP/SCCM sepsis definitions in surgical patients: a retrospective observational study
Manfred Weiss, Markus Huber-Lang, Michael Taenzer, et al.
Genomics
|
April 1, 1992
Chromosome mapping of the rod photoreceptor cGMP phosphodiesterase beta-subunit gene in mouse and human: tight linkage to the Huntington disease region (4p16.3)
M R Altherr, J J Wasmuth, M F Seldin, et al.
Scientific Reports
|
October 9, 2025
Using an electronic frailty index and patient reported outcomes to predict sarcopenia risk
Cody A Altherr, Xiao Luo, Haoran Ding, et al.
Genomics
|
May 20, 1995
Mapping of the gene for the Mel1a-melatonin receptor to human chromosome 4 (MTNR1A) and mouse chromosome 8 (Mtnr1a)
S A Slaugenhaupt, A L Roca, C B Liebert, et al.
American Journal of Medical Genetics
|
November 1, 1992
Molecular detection of a 4p deletion using PCR-based polymorphisms: a technique for the rapid detection of the Wolf-Hirschhorn syndrome
M R Altherr, J F Gusella, J J Wasmuth, et al.
Nutrition Today
|
October 18, 2021
Dietary Nitrate Supplementation and Exercise-Related Performance
Marissa N Baranauskas, Andrew R Coggan, Allison H Gruber, et al.
Genomics
|
December 1, 1991
A gene encoding a fibroblast growth factor receptor isolated from the Huntington disease gene region of human chromosome 4
L M Thompson, S Plummer, M Schalling, et al.
Human Molecular Genetics
|
October 1, 1996
The evolutionary distribution and structural organization of the homeobox-containing repeat D4Z4 indicates a functional role for the ancestral copy in the FSHD region
S T Winokur, U Bengtsson, J C Vargas, et al.
American Journal of Medical Genetics
|
March 17, 2001
First known microdeletion within the Wolf-Hirschhorn syndrome critical region refines genotype-phenotype correlation
A Rauch, S Schellmoser, C Kraus, et al.
Molecular and Cellular Probes
|
December 1, 1992
Assay by polymerase chain reaction (PCR) of multi-allele polymorphisms in the Huntington's disease region of chromosome 4
B A Allitto, A I McClatchey, G Barnes, et al.
Page
of 13