Publications by authors named "Carol L Clericuzio"

23Publications

A new syndrome with multiple capillary malformations, intractable seizures, and brain and limb anomalies.

Am J Med Genet A 2011 Feb;155A(2):301-6

Division of Developmental Pediatrics, Department of Pediatrics, Hospital for Sick Children, and Holland Bloorview Kids Rehabilitation Hospital, Toronto, Ontario, Canada.

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http://doi.wiley.com/10.1002/ajmg.a.33841
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http://dx.doi.org/10.1002/ajmg.a.33841DOI Listing
February 2011

Limb hyperplasia: case report of an unusual variant of Klippel-Trenaunay syndrome and review of the literature.

Cutis 2009 May;83(5):255-62

Department of Pathology, University of New Mexico Health Sciences Center, Albuquerque, NM 87131-0001, USA.

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May 2009

Diagnostic criteria and tumor screening for individuals with isolated hemihyperplasia.

Genet Med 2009 Mar;11(3):220-2

Department of Pediatrics, University of New Mexico Health Sciences Center, 1 University of New Mexico, Albuquerque, NM 87131-0001, USA.

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http://dx.doi.org/10.1097/GIM.0b013e31819436cfDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3111026PMC
March 2009

Acute lymphoblastic leukemia in a patient with Miller-Dieker syndrome.

J Pediatr Hematol Oncol 2008 Nov;30(11):865-8

Department of Pathology, University of New Mexico Health Sciences Center, Albuquerque, New Mexico, USA.

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http://dx.doi.org/10.1097/MPH.0b013e31818a958aDOI Listing
November 2008

A new hypothesis of OCA1B.

Am J Med Genet A 2008 Nov;146A(22):2968-70

UC Denver DNA Diagnostic Laboratory, Department of Pediatrics, UC Denver School of Medicine, Aurora, CO, USA.

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http://dx.doi.org/10.1002/ajmg.a.32539DOI Listing
November 2008

Two new patients with Curry-Jones syndrome with trichoblastoma and medulloblastoma suggest an etiologic role of the sonic hedgehog-patched-GLI pathway.

Am J Med Genet A 2008 Oct;146A(20):2589-97

Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri 63110, USA.

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http://dx.doi.org/10.1002/ajmg.a.32503DOI Listing
October 2008

Pierre Robin sequence associated with first trimester fetal tamoxifen exposure.

Am J Med Genet A 2008 Aug;146A(16):2141-4

University of New Mexico School of Medicine, Albuquerque, New Mexico 87131-0001, USA.

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http://dx.doi.org/10.1002/ajmg.a.32432DOI Listing
August 2008

Deaths due to choking in Prader-Willi syndrome.

Am J Med Genet A 2007 Mar;143A(5):484-7

Department of Pediatrics, Division of Medical Genetics, University of Utah, Salt Lake City, Utah 84132, USA.

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http://dx.doi.org/10.1002/ajmg.a.31502DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3243066PMC
March 2007

Risk for leukemia in infants without Down syndrome who have transient myeloproliferative disorder.

J Pediatr 2006 May;148(5):687-9

Department of Pediatrics, Division of Genetics and Metabolism, Stanford University Medical Center, Stanford, California, USA.

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http://dx.doi.org/10.1016/j.jpeds.2005.12.031DOI Listing
May 2006

Marshall-Smith syndrome: natural history and evidence of an osteochondrodysplasia with connective tissue abnormalities.

Am J Med Genet A 2005 Aug;137(2):117-24

Department of Pediatrics, Stanford University School of Medicine, Stanford, California, USA.

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http://dx.doi.org/10.1002/ajmg.a.30580DOI Listing
August 2005

Unexpected death and critical illness in Prader-Willi syndrome: report of ten individuals.

Am J Med Genet A 2004 Jan;124A(2):158-64

Department of Pediatrics, University of New Mexico, Albuquerque, New Mexico, USA.

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http://dx.doi.org/10.1002/ajmg.a.20370DOI Listing
January 2004

Athabascan brainstem dysgenesis syndrome.

Am J Med Genet A 2003 Jul;120A(2):169-73

Tuba City Indian Medical Center, Tuba City, Arizona 86045, USA.

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http://dx.doi.org/10.1002/ajmg.a.20087DOI Listing
July 2003