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Journal of Clinical Pathology
|
January 1, 1987
Aggregation of white cells and C-reactive protein: relation between these two indices in acute phase reaction
S Berliner, D Caspi, Y Neuman, et al.
Endoscopy International Open
|
August 15, 2018
Role of video capsule endoscopy in patients with constitutional mismatch repair deficiency (CMMRD) syndrome: report from the International CMMRD Consortium
Y Shimamura, C M Walsh, S Cohen, et al.
American Journal of Medical Genetics
|
September 20, 2001
Motivations and psychosocial impact of genetic testing for HNPCC
M J Esplen, L Madlensky, K Butler, et al.
Respiration; International Review of Thoracic Diseases
|
January 1, 1990
The state of leukocyte adhesiveness/aggregation in the peripheral blood of patients with respiratory tract infections
R Fadilah, S Berliner, D Kidron, et al.
Cytogenetics and Cell Genetics
|
January 1, 1979
Duplication of a segment of chromosome 3 in a subject with multiple congenital anomalies and a 47,XYY father, inversion of chromosomes 3 and 9 in the mother, and inversion of chromosome 9 in a brother. Repository identification Nos. GM-1253, GM-1252, and GM-1251
I S Pope, H C Thuline, M M Aronson, et al.
Cytogenetics and Cell Genetics
|
January 1, 1975
A ring 9 chromosome. Repository identification no. GM-166
M L Kistenmacher, H H Punnett, M Aronson, et al.
Cytogenetics and Cell Genetics
|
January 1, 1975
A (13;22) translocation, 46 chromosomes. Repository identification No. GM-627
H J Kim, K Hirschhorn, L Y Hsu, et al.
Cytogenetics and Cell Genetics
|
January 1, 1977
A culture with a derivative chromosome 10 from a paternal (10;16) translocation. Repository identification no. GM-1396
B Emanuel, E H Zackai, W J Mellman, et al.
Cytogenetics and Cell Genetics
|
January 1, 1978
A (14;20) translocation, unbalanced, from a subject with severe congenital anomalies. Respository identification No. GM-981
B S Emanuel, E Zackai, W J Mellman, et al.
Cytogenetics and Cell Genetics
|
January 1, 1978
Deletion in the long arm of chromosome 1 from a subject with multiple congenital anomalies. Respository identification No. GM-2025
G S Sekhon, R E Hillman, R Yu, et al.
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of 75
Search research articles
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Showing results (691-700 of 749) with videos related to
Sort By:
Page
of 75
Journal of Clinical Pathology
|
January 1, 1987
Aggregation of white cells and C-reactive protein: relation between these two indices in acute phase reaction
S Berliner, D Caspi, Y Neuman, et al.
Endoscopy International Open
|
August 15, 2018
Role of video capsule endoscopy in patients with constitutional mismatch repair deficiency (CMMRD) syndrome: report from the International CMMRD Consortium
Y Shimamura, C M Walsh, S Cohen, et al.
American Journal of Medical Genetics
|
September 20, 2001
Motivations and psychosocial impact of genetic testing for HNPCC
M J Esplen, L Madlensky, K Butler, et al.
Respiration; International Review of Thoracic Diseases
|
January 1, 1990
The state of leukocyte adhesiveness/aggregation in the peripheral blood of patients with respiratory tract infections
R Fadilah, S Berliner, D Kidron, et al.
Cytogenetics and Cell Genetics
|
January 1, 1979
Duplication of a segment of chromosome 3 in a subject with multiple congenital anomalies and a 47,XYY father, inversion of chromosomes 3 and 9 in the mother, and inversion of chromosome 9 in a brother. Repository identification Nos. GM-1253, GM-1252, and GM-1251
I S Pope, H C Thuline, M M Aronson, et al.
Cytogenetics and Cell Genetics
|
January 1, 1975
A ring 9 chromosome. Repository identification no. GM-166
M L Kistenmacher, H H Punnett, M Aronson, et al.
Cytogenetics and Cell Genetics
|
January 1, 1975
A (13;22) translocation, 46 chromosomes. Repository identification No. GM-627
H J Kim, K Hirschhorn, L Y Hsu, et al.
Cytogenetics and Cell Genetics
|
January 1, 1977
A culture with a derivative chromosome 10 from a paternal (10;16) translocation. Repository identification no. GM-1396
B Emanuel, E H Zackai, W J Mellman, et al.
Cytogenetics and Cell Genetics
|
January 1, 1978
A (14;20) translocation, unbalanced, from a subject with severe congenital anomalies. Respository identification No. GM-981
B S Emanuel, E Zackai, W J Mellman, et al.
Cytogenetics and Cell Genetics
|
January 1, 1978
Deletion in the long arm of chromosome 1 from a subject with multiple congenital anomalies. Respository identification No. GM-2025
G S Sekhon, R E Hillman, R Yu, et al.
Page
of 75