Research Letter

Keppen–Lubinsky syndrome: Expanding the phenotype†

  1. Lina Basel-Vanagaite1,2,*,
  2. Lisa Shaffer3,
  3. David Chitayat4,5

Article first published online: 16 JUL 2009

DOI: 10.1002/ajmg.a.32975

Issue

American Journal of Medical Genetics Part A

American Journal of Medical Genetics Part A

Volume 149A, Issue 8, pages 1827–1829, August 2009

Additional Information

How to Cite

Basel-Vanagaite, L., Shaffer, L. and Chitayat, D. (2009), Keppen–Lubinsky syndrome: Expanding the phenotype. Am. J. Med. Genet., 149A: 1827–1829. doi: 10.1002/ajmg.a.32975

Author Information

  1. 1

    Schneider Children's Medical Center of Israel, Raphael Recanati Genetics Institute, Rabin Medical Center, Beilinson Hospital, Petah Tikva, Israel

  2. 2

    Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel

  3. 3

    Signature Genomic Laboratories, Spokane, Washington

  4. 4

    Divisions of Clinical and Metabolic Genetics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada

  5. 5

    The Prenatal Diagnosis and Medical Genetics Program, Department of Obstetrics and Gynecology, Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada

*Raphael Recanati Genetics Institute, Rabin Medical Center, Beilinson Hospital, Petah Tikva 49100, Israel.

  1. †

    How to cite this article: Basel-Vanagaite L, Shaffer L, Chitayat D. 2009. Keppen–Lubinsky syndrome: Expanding the phenotype. Am J Med Genet Part A 149A:1827–1829.

Publication History

  1. Issue published online: 23 JUL 2009
  2. Article first published online: 16 JUL 2009
  3. Manuscript Accepted: 9 MAY 2009
  4. Manuscript Received: 1 MAR 2009

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