SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Pawel Borun, Marina De Rosa, Boguslaw Nedoszytko, Jaroslaw Walkowiak, Andrzej Plawski, Specific Alu elements involved in a significant percentage of copy number variations of the STK11 gene in patients with Peutz–Jeghers syndrome, Familial Cancer, 2015,

    CrossRef

  2. 2
    Graziella Di Grezia, Tiziana Romano, Francesco De Francesco, Francesco Somma, Gaetano Rea, Roberto Grassi, Gianluca Gatta, Breast ultrasound in the management of gynecomastia in Peutz–Jeghers syndrome in monozygotic twins: two case reports, Journal of Medical Case Reports, 2014, 8, 1, 440

    CrossRef

  3. 3
    Giuseppe Andrea Ferraro, Tiziana Romano, Francesco De Francesco, Anna Grandone, Francesco D’Andrea, Emanuele Miraglia del Giudice, Chiara Cataldo, Gianluca Gatta, Graziella Di Grezia, Laura Perrone, Gianfranco Nicoletti, Management of Prepubertal Gynecomastia in Two Monozygotic Twins With Peutz-Jeghers Syndrome: From Aromatase Inhibitors To Subcutaneous Mastectomy, Aesthetic Plastic Surgery, 2013, 37, 5, 1012

    CrossRef

  4. 4
    Hye Ran Yang, Jae Sung Ko, Jeong Kee Seo, Germline Mutation Analysis of STK11 Gene Using Direct Sequencing and Multiplex Ligation-Dependent Probe Amplification Assay in Korean Children with Peutz-Jeghers Syndrome, Digestive Diseases and Sciences, 2010, 55, 12, 3458

    CrossRef

  5. 5
    Anelia Horvath, Constantine A. Stratakis, Carney complex and lentiginosis, Pigment Cell & Melanoma Research, 2009, 22, 5
  6. 6
    Michael P. Kim, Douglas B. Evans, Thuy M. Vu, Jason B. Fleming, The Recognition and Surgical Management of Heritable Lesions of the Pancreas, Surgical Oncology Clinics of North America, 2009, 18, 1, 99

    CrossRef

  7. 7
    Martin Tobi, Michael Kam, Nadeem Ullah, Kashif Qureshi, Violeta Yordanova, James Hatfield, Suzanne E. G. Fligiel, Paula Sochacki, Thomas McGarrity, Carolyn Cole, Michael Lawson, Russell Jacoby, An Anti-adenoma Antibody, Adnab-9, May Reflect the Risk for Neoplastic Progression in Familial Hamartomatous Polyposis Syndromes, Digestive Diseases and Sciences, 2008, 53, 3, 723

    CrossRef

  8. 8
    E Chow, CJ Meldrum, R Crooks, F Macrae, AD Spigelman, RJ Scott, An updated mutation spectrum in an Australian series of PJS patients provides further evidence for only one gene locus, Clinical Genetics, 2006, 70, 5
  9. 9
    Michael Kam, Jorge Massare, Steven Gallinger, Joseph Kinzie, Donald Weaver, John D. Dingell, Susmita Esufali, Bharati Bapat, Martin Tobi, Peutz-Jeghers Syndrome Diagnosed in a Schizophrenic Patient with a Large Deletion in the STK11 Gene, Digestive Diseases and Sciences, 2006, 51, 9, 1567

    CrossRef

  10. 10
    L. Audí, N. Torán, C. Piró, M. Gussinyé, A. Carrascosa, Genetically Determined Gonadal Tumours in Children, Journal of Pediatric Endocrinology and Metabolism, 2005, 18, Supplement, 1215

    CrossRef

  11. 11
    Anders Merg, Henry T. Lynch, Jane F. Lynch, James R. Howe, Hereditary Colorectal Cancer-Part II, Current Problems in Surgery, 2005, 42, 5, 267

    CrossRef

  12. 12
    Stefan Aretz, Dietlinde Stienen, Siegfried Uhlhaas, Steffan Loff, Walter Back, Constanze Pagenstecher, D. Ross McLeod, Gail E. Graham, Elisabeth Mangold, René Santer, Peter Propping, Waltraut Friedl, High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome, Human Mutation, 2005, 26, 6
  13. 13
    Virpi Launonen, Mutations in the human LKB1/STK11 gene, Human Mutation, 2005, 26, 4
  14. 14
    Ian Roy Schreibman, Maria Baker, Christopher Amos, Thomas J. McGarrity, The Hamartomatous Polyposis Syndromes: A Clinical and Molecular Review, The American Journal of Gastroenterology, 2005, 100, 2, 476

    CrossRef

  15. 15
    Nicholas Hearle, Anneke Lucassen, Rubin Wang, Wendy Lim, Fiona Ross, Robert Wheeler, Isabella Moore, Janet Shipley, Richard Houlston, Mapping of a translocation breakpoint in a Peutz–Jeghers hamartoma to the putative PJS locus at 19q13.4 and mutation analysis of candidate genes in polyp and STK11-negative PJS cases, Genes, Chromosomes and Cancer, 2004, 41, 2
  16. 16
    Wolfgang G Ballhausen, Klaus Günther, Genetic screening for Peutz–Jeghers syndrome, Expert Review of Molecular Diagnostics, 2003, 3, 4, 471

    CrossRef

  17. 17
    Lianchun Kang, Xirong Zhao, Yongshuang Zhou, Yixing Jia, Suhai Kang, Zhu Chen, Min Zhao, Jiantao Cui, Wenmei Li, Anle Sun, Youyong Lu, Mutations analysis ofSTK 11 gene in Chinese families with Peutz-Jeghers syndrome, Chinese Science Bulletin, 2003, 48, 4, 333

    CrossRef

  18. 18
    Barbara A Leggett, Joanne P Young, Melissa Barker, Peutz–Jeghers syndrome: genetic screening, Expert Review of Anticancer Therapy, 2003, 3, 4, 518

    CrossRef

  19. 19
    RJ Scott, R Crooks, CJ Meldrum, L Thomas, CJA Smith, D Mowat, M McPhillips, AD Spigelman, Mutation analysis of the STK11/LKB1 gene and clinical characteristics of an Australian series of Peutz–Jeghers syndrome patients, Clinical Genetics, 2002, 62, 4
  20. 20
    Constantine A. Stratakis, Clinical genetics of multiple endocrine neoplasias, Carney complex and related syndromes, Journal of Endocrinological Investigation, 2001, 24, 5, 370

    CrossRef

  21. 21
    Abdalla A. Abed, Klaus Günther, Cornelia Kraus, Werner Hohenberger, Wolfgang G. Ballhausen, Mutation screening at the RNA level of the STK11/LKB1 gene in Peutz-Jeghers syndrome reveals complex splicing abnormalities and a novel mRNA isoform (STK11 c.597598insIVS4), Human Mutation, 2001, 18, 5
  22. 22
    Lisa A. Boardman, Mark R. Pittelkow, Fergus J. Couch, Daniel J. Schaid, Shannon K. McDonnell, Lawrence J. Burgart, David A. Ahlquist, J. Aidan Carney, David I. Schwartz, Stephen N. Thibodeau, Lynn C. Hartmann, Association of Peutz-Jeghers-like Mucocutaneous Pigmentation with Breast and Gynecologic Carcinomas in Women, Medicine, 2000, 79, 5, 293

    CrossRef

  23. 23
    Lisa A. Boardman, Fergus J. Couch, Lawrence J. Burgart, David Schwartz, Rebecca Berry, Shannon K. McDonnell, Daniel J. Schaid, Lynn C. Hartmann, Jennifer J. Schroeder, Constantine A. Stratakis, Stephen N. Thibodeau, Genetic heterogeneity in Peutz-Jeghers syndrome, Human Mutation, 2000, 16, 1
  24. 24
    Jindong Chen, Annika Lindblom, Germline mutation screening of the STK11/LKB1 gene in familial breast cancer with LOH on 19p, Clinical Genetics, 2000, 57, 5