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Cancer Genetics and Cytogenetics
|
November 1, 1993
Deletion 7q22 in uterine leiomyoma. A cytogenetic review
Y Y Ozisik, A M Meloni, U Surti, et al.
Cancer Genetics and Cytogenetics
|
June 1, 1983
Cytogenetic findings in congenital leukemia: case report and review of the literature
R Abe, D Ryan, A Cecalupo, et al.
Nature Genetics
|
March 1, 1993
A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescens
K Kajiwara, M A Sandberg, E L Berson, et al.
Analytical Biochemistry
|
November 1, 1985
Quantitative solubilization of nonhistone chromosomal proteins without denaturation using zwitterionic detergents
Y Matuo, S Matsui, N Nishi, et al.
Cancer Chemotherapy and Pharmacology
|
January 1, 1991
Accumulation of estramustine and estromustine in adipose tissue of rats and humans
P O Gunnarsson, S B Andersson, A A Sandberg, et al.
American Journal of Hematology
|
September 18, 2001
Hematologic masquerade of rhabdomyosarcoma
A A Sandberg, J F Stone, L Czarnecki, et al.
Journal of the National Cancer Institute
|
April 1, 1984
Chromosome changes in soft tissue sarcomas
R Becher, N Wake, Z Gibas, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
January 1, 1991
Ocular findings in patients with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (Pro-23-His)
E L Berson, B Rosner, M A Sandberg, et al.
Gynecologic Oncology
|
August 1, 1990
Three related near-haploid clones in a primary endometrioid carcinoma of the ovary
C Sreekantaiah, K Crickard, U Crickard, et al.
American Journal of Ophthalmology
|
November 15, 1989
An electroretinographic and molecular genetic study of X-linked cone degeneration
E Reichel, A M Bruce, M A Sandberg, et al.
Page
of 94
Search research articles
Search
Showing results (461-470 of 934) with videos related to
Sort By:
Page
of 94
Cancer Genetics and Cytogenetics
|
November 1, 1993
Deletion 7q22 in uterine leiomyoma. A cytogenetic review
Y Y Ozisik, A M Meloni, U Surti, et al.
Cancer Genetics and Cytogenetics
|
June 1, 1983
Cytogenetic findings in congenital leukemia: case report and review of the literature
R Abe, D Ryan, A Cecalupo, et al.
Nature Genetics
|
March 1, 1993
A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescens
K Kajiwara, M A Sandberg, E L Berson, et al.
Analytical Biochemistry
|
November 1, 1985
Quantitative solubilization of nonhistone chromosomal proteins without denaturation using zwitterionic detergents
Y Matuo, S Matsui, N Nishi, et al.
Cancer Chemotherapy and Pharmacology
|
January 1, 1991
Accumulation of estramustine and estromustine in adipose tissue of rats and humans
P O Gunnarsson, S B Andersson, A A Sandberg, et al.
American Journal of Hematology
|
September 18, 2001
Hematologic masquerade of rhabdomyosarcoma
A A Sandberg, J F Stone, L Czarnecki, et al.
Journal of the National Cancer Institute
|
April 1, 1984
Chromosome changes in soft tissue sarcomas
R Becher, N Wake, Z Gibas, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
January 1, 1991
Ocular findings in patients with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (Pro-23-His)
E L Berson, B Rosner, M A Sandberg, et al.
Gynecologic Oncology
|
August 1, 1990
Three related near-haploid clones in a primary endometrioid carcinoma of the ovary
C Sreekantaiah, K Crickard, U Crickard, et al.
American Journal of Ophthalmology
|
November 15, 1989
An electroretinographic and molecular genetic study of X-linked cone degeneration
E Reichel, A M Bruce, M A Sandberg, et al.
Page
of 94