W. Stanley

发表

Bleomycin hypersensitivity in dyskeratosis congenita fibroblasts, lymphocytes, and transformed lymphoblasts.

G. Pai, Y. Yan, D. Debauche, 1989, Cytogenetics and cell genetics.

Enhanced G2 chromatid radiosensitivity in dyskeratosis congenita fibroblasts.

G. Pai, D. Debauche, W. Stanley, 1990, American journal of human genetics.

Prenatal diagnosis of Pallister–Killian syndrome: Resolution of cytogenetic ambiguity by use of fluorescent in situ hybridization

K. Rosenbaum, H. Stern, W. Stanley, 1992, Prenatal diagnosis.

The accuracy of chromosomal microarray testing for identification of embryonic mosaicism in human blastocysts

V. Novik, K. Tran, H. Stern, 2014, Molecular Cytogenetics.

Spontaneous and 4-nitroquinoline 1-oxide-induced G2 chromosome aberrations in lymphoblasts from familial melanoma patients.

N. Hayward, W. Stanley, G. Lu, 1989, Cancer genetics and cytogenetics.

Characterization and clinical implications of marker chromosomes identified at prenatal diagnosis

Marilyn M. Li, L. Fallon, W. Stanley, 2000, Prenatal diagnosis.

Sensitivity of detection of B-cell lymphoma in bone marrow by fluorescence in situ hybridization.

W. Stanley, C. Juenger, 2002, Cancer genetics and cytogenetics.

Short communication Sensitivity of detection of B-cell lymphoma in bone marrow by fluorescence in situ hybridization

W. Stanley, C. Juenger, 2002 .

Epidermal growth factor receptor expression in a retinoic acid-treated human melanoma cell line.

Y. Yongshan, D. Debauche, W. Stanley, 1990, Cancer genetics and cytogenetics.

The In Vitro Growth, Heterotranspiantation, and 1mmunoh istochemical Characterization of the Blastemal Component of Wi/ms' Tumor

A. Garvin, J. Sullivan, W. Stanley, 2007 .

The in vitro growth, heterotransplantation, and immunohistochemical characterization of the blastemal component of Wilms' tumor.

D. Sens, A. Garvin, J. Sullivan, 1987, The American journal of pathology.

The in vitro growth, heterotransplantation, and differentiation of a human rhabdomyosarcoma cell line.

D. Sens, A. Garvin, J. Sullivan, 1986, The American journal of pathology.

BS I-B4 isolectin as a probe for an investigation of membrane alterations and transformation phenotypes of mouse L cells.

E. Chu, W. Stanley, 1981, Journal of cell science.

Effect of differentiating agents on nucleolar organizer region activity in human melanoma cells.

Y. Yan, W. Stanley, 1988, Cancer genetics and cytogenetics.

Interaction of wild-type and variant mouse 3T3 cells with lectins from Bandeiraea simplicifolia seeds.

I. Goldstein, D. Blake, B. P. Peters, 1979, Proceedings of the National Academy of Sciences of the United States of America.

Longitudinal cytogenetic study of metaphase and interphase cells in childhood monosomy 7 syndrome.

N. Seibel, B. A. Murphy, P. Dinndorf, 1992, Cancer genetics and cytogenetics.

Aggressive bladder carcinoma in an adolescent. Report of a case with immunohistochemical, cytogenetic, and flow cytometric characterization.

T. Gansler, A. Garvin, A. Scott, 1989, The American journal of surgical pathology.

Mosaic 5p tetrasomy.

C. Powell, C. Samango-Sprouse, B. A. Murphy, 1993, American journal of medical genetics.

Interphase FISH and morphologic analysis of AML.

W. Stanley, L. Pagliaro, 1993, Cancer genetics and cytogenetics.

Assignment of the gene for phosphoribosylpyrophosphate amidotransferase to the pter leads to q21 region of human chromosome 4.

E. Chu, W. Stanley, 1978, Cytogenetics and cell genetics.

Relationship between mitotic delay and the minimum dose rate of X irradiation required to stop cell proliferation.

P. Yi, W. Stanley, W. Lee, 1993, Radiation research.

Prenatal diagnosis of Smith–Lemli–Opitz syndrome in a pregnancy with low maternal serum oestriol and a sex‐reversed fetus

R. Kelley, G. Berkovitz, H. Stern, 1999, Prenatal diagnosis.

Constitutional inversion of chromosome 7 and hematologic cancers.

S. Burkett, J. Lobel, N. Shah, 1997, Cancer genetics and cytogenetics.

Isochromosome 11q in a case of Ewing's sarcoma.

A. Garvin, W. Stanley, D. D. Bennett, 1987, Cancer Genetics and Cytogenetics.

Incidental detection of premature centromere separation in amniocytes associated with a mild form of Roberts syndrome

K. McNeal, Y. Yongshan, G. Pai, 1988, Prenatal diagnosis.