P. Vantuinen

发表

Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas.

D. Ledbetter, Y. Nakamura, B. Vogelstein, 1989, Science.

Molecular cloning and characterization of a cDNA for human granulocyte colony-stimulating factor (G-CSF) from a glioblastoma multiforme cell line and localization of the G-CSF gene to chromosome band 17q21.

P. Nowell, D. Ledbetter, A. Palumbo, 1987, Oncogene research.

The human PECAM1 gene maps to 17q23.

P. N. Rao, P. Vantuinen, N. Kirschbaum, 1996, Genomics.

Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome region.

T. J. Robinson, D. Ledbetter, R. Wolff, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Morphologic and cytogenetic variables affect the flow cytometric recovery of plasma cell myeloma cells in bone marrow aspirates

P. Vantuinen, C. Cogbill, A. Harrington, 2015, International journal of laboratory hematology.

Recurrent giant cranial desmoid tumor in a 3-year-old boy with familial adenomatous polyposis requiring bifrontoparietal cranioplasty: case report.

P. Vantuinen, S. Lew, Luyuan Li, 2016, Journal of neurosurgery. Pediatrics.

The importance of communicating histories of gender assignment and reassignment to genetic laboratories

P. Vantuinen, Jess F. Peterson, John W Grignon, 2017, Genetics in Medicine.

Isolation of cDNA clones for the catalytic gamma subunit of mouse muscle phosphorylase kinase: expression of mRNA in normal and mutant Phk mice.

C. Caskey, P. Vantuinen, J. Chamberlain, 1987, Proceedings of the National Academy of Sciences of the United States of America.

Structural analysis of a hepatitis B virus genome integrated into chromosome 17p of a human hepatocellular carcinoma

D. Ledbetter, L. Donehower, B. Slagle, 1988, Journal of virology.

Mantle Cell Lymphoma in Lymph Nodes with Metastatic Small Cell Carcinoma of Lung: A Diagnostic and Treatment Dilemma

C. Chang, P. Vantuinen, V. Shidham, 2004, Leukemia & lymphoma.

Preimplantation Genetic Testing: Current Status and Future Prospects

D. Bick, P. Vantuinen, E. Lau, 2012 .

A multicenter investigation with interphase fluorescence in situ hybridization using X- and Y-chromosome probes.

S. Schwartz, A. Zinsmeister, G. Vance, 1998, American journal of medical genetics.

Inheritance of a Balanced t(12;20)(q24.33;p12.2) and Unbalanced der(13)t(7;13)(p21.3;q33.2) from a Maternally Derived Double Balanced Translocation Carrier

G. Geddes, P. Vantuinen, Donald G Basel, 2017, Journal of Pediatric Genetics.

The anonymous polymorphic DNA clone D1S1, previously mapped to human chromosome 1p36 by in situ hybridization, is from chromosome 3 and is duplicated on chromosome 1.

D. Ledbetter, S. Daiger, P. Vantuinen, 1986, American journal of human genetics.

Molecular characterization of human and bovine rod photoreceptor cGMP phosphodiesterase alpha-subunit and chromosomal localization of the human gene.

D. Ledbetter, R. Davis, J. Wasmuth, 1990, Genomics.

The human apolipoprotein B-100 gene: a highly polymorphic gene that maps to the short arm of chromosome 2.

D. Ledbetter, S. Daiger, A. Gotto, 1985, Biochemical and biophysical research communications.

Mapping of human methylmalonyl CoA mutase (MUT) locus on chromosome 6.

D. Ledbetter, H. Zoghbi, P. Vantuinen, 1988, American journal of human genetics.

Concomitant 11p15.4‐p15.5 duplication and terminal 22q13.33 deletion in a patient with features of Beckwith–Wiedemann syndrome

U. Broeckel, D. Bick, G. Geddes, 2016, American journal of medical genetics. Part A.

Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndrome.

D. Ledbetter, Y. Nakamura, W. Dobyns, 1988, American journal of human genetics.

Human hepatic lipase. Cloned cDNA sequence, restriction fragment length polymorphisms, chromosomal localization, and evolutionary relationships with lipoprotein lipase and pancreatic lipase.

D. Ledbetter, Wen-Hsiung Li, C. Luo, 1988, The Journal of biological chemistry.

Identification of High-risk Cryptic CRLF2 Rearrangements in B-Cell Acute Lymphoblastic Leukemia Utilizing an FGFR3/IGH Dual-Color Dual-Fusion DNA Probe Set

P. Vantuinen, Jess F. Peterson, M. Burke, 2017, Journal of pediatric hematology/oncology.

Malignant Gastrointestinal Neuroectodermal Tumor: Clinicopathologic, Immunohistochemical, Ultrastructural, and Molecular Analysis of 16 Cases With a Reappraisal of Clear Cell Sarcoma-like Tumors of the Gastrointestinal Tract

S. Suster, P. Vantuinen, J. Hornick, 2012, The American journal of surgical pathology.

Clinicopathologic analysis of the impact of CD23 expression in plasma cell myeloma with t(11;14)(q13;q32).

P. Vantuinen, A. Harrington, S. Kroft, 2011, Annals of diagnostic pathology.

Proliferation centers in bone marrows involved by chronic lymphocytic leukemia/small lymphocytic lymphoma: a clinicopathologic analysis.

P. Vantuinen, A. Harrington, S. Kroft, 2016, Annals of diagnostic pathology.

Molecular Detection ofMicroscopic andSubmicroscopic Deletions Associated withMiller-Dieker Syndrome

P. Vantuinen, 1988 .

Molecular cloning and chromosomal localization of human 4-beta-galactosyltransferase.

D. Ledbetter, P. Vantuinen, B. Bunnell, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Follicular lymphoma transformation to dual translocated Burkitt-like lymphoma: improved disease control associated with radiation therapy

P. Vantuinen, K. Christians, C. Schultz, 2009, International journal of hematology.

Preimplantation Genetic Testing: Current Status and Future Prospects

D. Bick, P. Vantuinen, E. Lau, 2012 .

S. Suster, P. Vantuinen, J. Hornick, 2012, The American journal of surgical pathology.