Darrel J. Waggoner to Developmental Disabilities
This is a "connection" page, showing publications Darrel J. Waggoner has written about Developmental Disabilities.
Connection Strength
1.005
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Paternal deletion 6q24.3: a new congenital anomaly syndrome associated with intrauterine growth failure, early developmental delay and characteristic facial appearance. Am J Med Genet A. 2008 Feb 01; 146A(3):354-60.
Score: 0.261
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NSD1 analysis for Sotos syndrome: insights and perspectives from the clinical laboratory. Genet Med. 2005 Oct; 7(8):524-33.
Score: 0.222
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Familial pyloric stenosis associated with developmental delays. J Pediatr Gastroenterol Nutr. 2005 Jul; 41(1):129-32.
Score: 0.219
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A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects. Neurogenetics. 2016 07; 17(3):173-8.
Score: 0.116
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Reciprocal deletion and duplication at 2q23.1 indicates a role for MBD5 in autism spectrum disorder. Eur J Hum Genet. 2014 Jan; 22(1):57-63.
Score: 0.094
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Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. Am J Hum Genet. 2010 May 14; 86(5):749-64.
Score: 0.077
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Two Children with macrocephaly, developmental delay, and PTEN mutation. Clin Pediatr (Phila). 2009 Jan; 48(1):89-92.
Score: 0.017