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Genomics
|
January 1, 1994
Genetic heterogeneity among craniosynostosis syndromes: mapping the Saethre-Chotzen syndrome locus between D7S513 and D7S516 and exclusion of Jackson-Weiss and Crouzon syndrome loci from 7p
A F Lewanda, M M Cohen, C E Jackson, et al.
American Journal of Medical Genetics
|
October 1, 1993
Saethre-Chotzen syndrome with familial translocation at chromosome 7p22
C S Reid, L E McMorrow, D M McDonald-McGinn, et al.
IEEE Transactions on Medical Imaging
|
November 10, 2001
Enhancement of contrast echocardiography by image variability analysis
B J Fetics, E Y Wong, T Murabayashi, et al.
American Journal of Hematology
|
April 1, 1985
Increased numbers of marrow basophils may be associated with a t(6;9) in ANLL
M G Pearson, J W Vardiman, M M Le Beau, et al.
Medical Care
|
December 1, 1995
A population-based health information system
N P Roos, C D Black, N Frohlich, et al.
The Journal of Pediatrics
|
February 1, 1986
Further delineation of Weaver syndrome
H H Ardinger, J W Hanson, M J Harrod, et al.
Nature Genetics
|
August 1, 1996
Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome
K A Przylepa, W Paznekas, M Zhang, et al.
QJM : Monthly Journal of the Association of Physicians
|
July 19, 2011
Use of variability in national and regional data to estimate the prevalence of lymphangioleiomyomatosis
E C Harknett, W Y C Chang, S Byrnes, et al.
Human Molecular Genetics
|
September 25, 1997
A novel phenotypic pattern in X-linked inheritance: craniofrontonasal syndrome maps to Xp22
G J Feldman, D E Ward, E Lajeunie-Renier, et al.
American Journal of Human Genetics
|
March 1, 1997
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome
M Muenke, K W Gripp, D M McDonald-McGinn, et al.
Page
of 45
Search research articles
Search
Showing results (441-450 of 450) with videos related to
Sort By:
Page
of 45
You have reached the last page of results.
This site can display upto 450 results.
Genomics
|
January 1, 1994
Genetic heterogeneity among craniosynostosis syndromes: mapping the Saethre-Chotzen syndrome locus between D7S513 and D7S516 and exclusion of Jackson-Weiss and Crouzon syndrome loci from 7p
A F Lewanda, M M Cohen, C E Jackson, et al.
American Journal of Medical Genetics
|
October 1, 1993
Saethre-Chotzen syndrome with familial translocation at chromosome 7p22
C S Reid, L E McMorrow, D M McDonald-McGinn, et al.
IEEE Transactions on Medical Imaging
|
November 10, 2001
Enhancement of contrast echocardiography by image variability analysis
B J Fetics, E Y Wong, T Murabayashi, et al.
American Journal of Hematology
|
April 1, 1985
Increased numbers of marrow basophils may be associated with a t(6;9) in ANLL
M G Pearson, J W Vardiman, M M Le Beau, et al.
Medical Care
|
December 1, 1995
A population-based health information system
N P Roos, C D Black, N Frohlich, et al.
The Journal of Pediatrics
|
February 1, 1986
Further delineation of Weaver syndrome
H H Ardinger, J W Hanson, M J Harrod, et al.
Nature Genetics
|
August 1, 1996
Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome
K A Przylepa, W Paznekas, M Zhang, et al.
QJM : Monthly Journal of the Association of Physicians
|
July 19, 2011
Use of variability in national and regional data to estimate the prevalence of lymphangioleiomyomatosis
E C Harknett, W Y C Chang, S Byrnes, et al.
Human Molecular Genetics
|
September 25, 1997
A novel phenotypic pattern in X-linked inheritance: craniofrontonasal syndrome maps to Xp22
G J Feldman, D E Ward, E Lajeunie-Renier, et al.
American Journal of Human Genetics
|
March 1, 1997
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome
M Muenke, K W Gripp, D M McDonald-McGinn, et al.
Page
of 45