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Gynecologic Oncology|August 28, 2010
A critical re-appraisal of BRCA1 methylation studies in ovarian cancerEmir Senturk, Samantha Cohen, Peter R Dottino, et al.
Carcinogenesis|February 5, 2000
Leukocyte common-antigen-related tyrosine phosphatase receptor: altered expression of mRNA and protein in the New England Deaconess Hospital rat line exhibiting spontaneous pheochromocytomaT Yang, J A Martignetti, S M Massa, et al.
Pediatrics|August 14, 2013
First successful use of eltrombopag before surgery in a child with MYH9-related thrombocytopeniaRemi Favier, Joffrey Feriel, Marie Favier, et al.
Journal of Human Genetics|September 25, 1999
Isolation, characterization, and mapping of four novel polymorphic markers and an H3.3B pseudogene to chromosome 9p21-22E Aliprandis, J Harris, B Yoo, et al.
Pediatric Radiology|September 1, 1996
Diaphyseal medullary stenosis (sclerosis) with bone malignancy (malignant fibrous histiocytoma): Hardcastle syndromeK I Norton, J M Wagreich, L Granowetter, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 26, 1994
Rodent BC1 RNA gene as a master gene for ID element amplificationJ Kim, J A Martignetti, M R Shen, et al.
Plos One|September 17, 2010
Nucleo-cytoplasmic localization domains regulate Krüppel-like factor 6 (KLF6) protein stability and tumor suppressor functionEstefanía Rodríguez, Nana Aburjania, Nolan M Priedigkeit, et al.
Clinical Dysmorphology|March 14, 2007
Torg-Winchester syndrome: lack of efficacy of pamidronate therapyShubha R Phadke, Maria Ramirez, Analisa DiFeo, et al.
Genes, Chromosomes & Cancer|December 29, 1999
Malignant fibrous histiocytoma: inherited and sporadic forms have loss of heterozygosity at chromosome bands 9p21-22-evidence for a common genetic defectJ A Martignetti, B D Gelb, H Pierce, et al.
European Journal of Human Genetics : EJHG|November 6, 2008
A novel matrix metalloproteinase 2 (MMP2) terminal hemopexin domain mutation in a family with multicentric osteolysis with nodulosis and arthritis with cardiac defectsBeyhan Tuysuz, Rebecca Mosig, Gürkan Altun, et al.
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