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Cancer Research
|
May 1, 1987
Quantitative assay of human T-cell leukemia/lymphoma virus transformation
S L Graziano, B M Lehr, S A Merl, et al.
American Journal of Human Genetics
|
June 23, 1998
Linkage and association between inflammatory bowel disease and a locus on chromosome 12
R H Duerr, M M Barmada, L Zhang, et al.
Journal of Pediatric Surgery
|
March 22, 2000
RNA differential display of scarless wound healing in fetal rabbit indicates downregulation of a CCT chaperonin subunit and upregulation of a glycophorin-like gene transcript
D L Darden, F Z Hu, M D Ehrlich, et al.
Human Molecular Genetics
|
August 1, 1995
Crouzon syndrome: mutations in two spliceoforms of FGFR2 and a common point mutation shared with Jackson-Weiss syndrome
M C Gorry, R A Preston, G J White, et al.
The American Journal of Gastroenterology
|
July 1, 1997
Clinical characteristics of hereditary pancreatitis in a large family, based on high-risk haplotype. The Midwest Multicenter Pancreatic Study Group (MMPSG)
M J Sossenheimer, C E Aston, R A Preston, et al.
JAMA
|
May 24, 1995
Molecular analysis of bacterial pathogens in otitis media with effusion
J C Post, R A Preston, J J Aul, et al.
Journal of Clinical Microbiology
|
February 11, 2011
Adenoid reservoir for pathogenic biofilm bacteria
L Nistico, R Kreft, A Gieseke, et al.
Nature Genetics
|
October 1, 1996
Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene
D C Whitcomb, M C Gorry, R A Preston, et al.
Gastroenterology
|
June 1, 1996
A gene for hereditary pancreatitis maps to chromosome 7q35
D C Whitcomb, R A Preston, C E Aston, et al.
JAMA
|
July 13, 2000
Mapping of a gene for severe pediatric gastroesophageal reflux to chromosome 13q14
F Z Hu, R A Preston, J C Post, et al.
Page
of 8
Search research articles
Search
Showing results (71-80 of 80) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 80 results.
Cancer Research
|
May 1, 1987
Quantitative assay of human T-cell leukemia/lymphoma virus transformation
S L Graziano, B M Lehr, S A Merl, et al.
American Journal of Human Genetics
|
June 23, 1998
Linkage and association between inflammatory bowel disease and a locus on chromosome 12
R H Duerr, M M Barmada, L Zhang, et al.
Journal of Pediatric Surgery
|
March 22, 2000
RNA differential display of scarless wound healing in fetal rabbit indicates downregulation of a CCT chaperonin subunit and upregulation of a glycophorin-like gene transcript
D L Darden, F Z Hu, M D Ehrlich, et al.
Human Molecular Genetics
|
August 1, 1995
Crouzon syndrome: mutations in two spliceoforms of FGFR2 and a common point mutation shared with Jackson-Weiss syndrome
M C Gorry, R A Preston, G J White, et al.
The American Journal of Gastroenterology
|
July 1, 1997
Clinical characteristics of hereditary pancreatitis in a large family, based on high-risk haplotype. The Midwest Multicenter Pancreatic Study Group (MMPSG)
M J Sossenheimer, C E Aston, R A Preston, et al.
JAMA
|
May 24, 1995
Molecular analysis of bacterial pathogens in otitis media with effusion
J C Post, R A Preston, J J Aul, et al.
Journal of Clinical Microbiology
|
February 11, 2011
Adenoid reservoir for pathogenic biofilm bacteria
L Nistico, R Kreft, A Gieseke, et al.
Nature Genetics
|
October 1, 1996
Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene
D C Whitcomb, M C Gorry, R A Preston, et al.
Gastroenterology
|
June 1, 1996
A gene for hereditary pancreatitis maps to chromosome 7q35
D C Whitcomb, R A Preston, C E Aston, et al.
JAMA
|
July 13, 2000
Mapping of a gene for severe pediatric gastroesophageal reflux to chromosome 13q14
F Z Hu, R A Preston, J C Post, et al.
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of 8