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Title
Molecular Mechanisms of Childhood Overgrowth
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
Volume 163, Issue 2, Pages 71-75
Publisher
Wiley
Online
2013-04-19
DOI
10.1002/ajmg.c.31362
References
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- Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility
- (2012) Dewi Astuti et al. NATURE GENETICS
- Mutations in EZH2 Cause Weaver Syndrome
- (2011) William T. Gibson et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Overgrowth of prenatal onset associated with submicroscopic 9q22.3 deletion
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- A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features
- (2011) A-M Molin et al. JOURNAL OF MEDICAL GENETICS
- A Mosaic Activating Mutation inAKT1Associated with the Proteus Syndrome
- (2011) Marjorie J. Lindhurst et al. NEW ENGLAND JOURNAL OF MEDICINE
- Distinct Effects of Allelic NFIX Mutations on Nonsense-Mediated mRNA Decay Engender Either a Sotos-like or a Marshall-Smith Syndrome
- (2010) Valérie Malan et al. AMERICAN JOURNAL OF HUMAN GENETICS
- 3.2 Mb microdeletion in chromosome 7 bands q22.2–q22.3 associated with overgrowth and delayed bone age
- (2010) Vera Uliana et al. European Journal of Medical Genetics
- 15q overgrowth syndrome: A newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15q
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- Array-based comparative genomic hybridization identifies a high frequency of copy number variations in patients with syndromic overgrowth
- (2009) Valérie Malan et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- PTEN and the PI3-Kinase Pathway in Cancer
- (2008) Nader Chalhoub et al. Annual Review of Pathology-Mechanisms of Disease
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