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American Academy of Pediatrics
Article

Use of the National Institutes of Health Criteria for Diagnosis of Neurofibromatosis 1 in Children

Kimberly DeBella, Jacek Szudek and Jan Marshall Friedman
Pediatrics March 2000, 105 (3) 608-614; DOI: https://doi.org/10.1542/peds.105.3.608
Kimberly DeBella
1From the Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
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Jacek Szudek
1From the Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
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Jan Marshall Friedman
1From the Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
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Article Information

vol. 105 no. 3 608-614
DOI 
https://doi.org/10.1542/peds.105.3.608
PubMed 
10699117

Published By 
American Academy of Pediatrics
Print ISSN 
0031-4005
Online ISSN 
1098-4275
History 
  • Received February 18, 1999
  • Accepted June 14, 1999
  • Published online March 1, 2000.

Copyright & Usage 
Copyright © 2000 American Academy of Pediatrics

Author Information

  1. Kimberly DeBella,
  2. Jacek Szudek, and
  3. Jan Marshall Friedman, MD, PhD
  1. 1 From the Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
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Pediatrics
Vol. 105, Issue 3
1 Mar 2000
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Use of the National Institutes of Health Criteria for Diagnosis of Neurofibromatosis 1 in Children
Kimberly DeBella, Jacek Szudek, Jan Marshall Friedman
Pediatrics Mar 2000, 105 (3) 608-614; DOI: 10.1542/peds.105.3.608

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Use of the National Institutes of Health Criteria for Diagnosis of Neurofibromatosis 1 in Children
Kimberly DeBella, Jacek Szudek, Jan Marshall Friedman
Pediatrics Mar 2000, 105 (3) 608-614; DOI: 10.1542/peds.105.3.608
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  • Health Supervision for Children With Neurofibromatosis Type 1
  • Constitutional mismatch repair deficiency as a differential diagnosis of neurofibromatosis type 1: consensus guidelines for testing a child without malignancy
  • Clinical Images: Imaging Manifestations of Orbital Neurofibromatosis Type 1
  • Optic Pathway Glioma and Cerebral Focal Abnormal Signal Intensity in Patients with Neurofibromatosis Type 1: Characteristics, Treatment Choices and Follow-up in 134 Affected Individuals and a Brief Review of the Literature
  • Perioperative Management of Neurofibromatosis Type 1
  • Cerebral Arteriopathy in Children With Neurofibromatosis Type 1
  • Visual Diagnosis: A Child Who Has Hyperpigmented Spots and a Forearm Deformity
  • Health Supervision for Children With Neurofibromatosis
  • Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1
  • Evaluation of genotype-phenotype correlations in neurofibromatosis type 1
  • A child with axillary freckling and cafe au lait spots
  • Neurofibromatosis type 1 and sporadic optic gliomas
  • Retroviral Integration at the Epi1Locus Cooperates with Nf1 Gene Loss in the Progression to Acute Myeloid Leukemia
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