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Cancer Genetics and Cytogenetics|November 1, 1993
Deletion 7q22 in uterine leiomyoma. A cytogenetic reviewY 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 literatureR 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 albescensK Kajiwara, M A Sandberg, E L Berson, et al.Analytical Biochemistry|November 1, 1985
Quantitative solubilization of nonhistone chromosomal proteins without denaturation using zwitterionic detergentsY 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 humansP O Gunnarsson, S B Andersson, A A Sandberg, et al.American Journal of Hematology|September 18, 2001
Hematologic masquerade of rhabdomyosarcomaA A Sandberg, J F Stone, L Czarnecki, et al.Journal of the National Cancer Institute|April 1, 1984
Chromosome changes in soft tissue sarcomasR 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 ovaryC Sreekantaiah, K Crickard, U Crickard, et al.American Journal of Ophthalmology|November 15, 1989
An electroretinographic and molecular genetic study of X-linked cone degenerationE Reichel, A M Bruce, M A Sandberg, et al.Pageof 559