Braddock-Carey syndrome: A 21q22 contiguous gene syndrome encompassingRUNX1-Reference-Cited by-同舟云学术

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Braddock-Carey syndrome: A 21q22 contiguous gene syndrome encompassingRUNX1

Published:2016-08-23 Issue:10 Volume:170 Page:2580-2586
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Braddock Stephen R.¹²,South Sarah T.³⁴,Schiffman Joshua D.⁵,Longhurst Maria⁴,Rowe Leslie R.⁴,Carey John C.⁵

Affiliation:

1. Division of Medical Genetics, Department of Pediatrics; Saint Louis University; Saint Louis Missouri

2. SSM Cardinal Glennon Children's Hospital; Saint Louis Missouri

3. Department of Pathology; University of Utah; Salt Lake City Utah

4. ARUP Laboratories; University of Utah; Salt Lake City Utah

5. Department of Pediatrics; University of Utah; Salt Lake City Utah

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference21 articles.

1. A new syndrome: Congenital thrombocytopenia, Robin sequence, agenesis of the corpus callosum, distinctive facies and developmental delay;Braddock;Clin Dysmorphol,1994

2. Braddock SR Schiffman JD South ST Carey JC. 2011

3. Monosomy 21q22.11-q22.13 presenting as a Fanconi anemia phenotype;Byrd;Am J Med Genet Part A,2011

4. Runx1 determines nociceptive sensory neuron phenotype and is required for thermal and neuropathic pain;Chen;Neuron,2006

5. A neonate with congenital amegakaryocytic thrombocytopenia associated with a chromosomal microdeletion at 21q22.11 including the gene RUNX1;Christensen;J Perinatol,2013

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