Kenton Holden to Abnormalities, Multiple
This is a "connection" page, showing publications Kenton Holden has written about Abnormalities, Multiple.
Connection Strength
1.089
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Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family. J Child Neurol. 2008 Aug; 23(8):901-5.
Score: 0.284
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Facial hemangioma, and associated malformations: a case report. Neuropediatrics. 2004 Jun; 35(3):194-7.
Score: 0.213
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A novel familial autosomal dominant mutation in ARID1B causing neurodevelopmental delays, short stature, and dysmorphic features. Am J Med Genet A. 2016 12; 170(12):3313-3318.
Score: 0.124
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Roberts/pseudothalidomide syndrome and normal intelligence: approaches to diagnosis and management. Dev Med Child Neurol. 1992 Jun; 34(6):534-9.
Score: 0.093
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Microdeletion at 4q21.3 is associated with intellectual disability, dysmorphic facies, hypotonia, and short stature. Am J Med Genet A. 2011 Sep; 155A(9):2146-53.
Score: 0.087
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Natural history of Christianson syndrome. Am J Med Genet A. 2010 Nov; 152A(11):2775-83.
Score: 0.083
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Expanding CEP290 mutational spectrum in ciliopathies. Am J Med Genet A. 2009 Oct; 149A(10):2173-80.
Score: 0.077
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A novel in-frame deletion in ARX is associated with lissencephaly with absent corpus callosum and hypoplastic genitalia. Am J Med Genet A. 2005 Sep 15; 138(1):70-2.
Score: 0.058
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Developmental neural abnormalities and seizures in epidermal nevus syndrome. Dev Med Child Neurol. 1996 Aug; 38(8):716-23.
Score: 0.031
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Seizures and X-linked intellectual disability. Eur J Med Genet. 2012 May; 55(5):307-12.
Score: 0.023
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Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome. Am J Hum Genet. 2008 Aug; 83(2):170-9.
Score: 0.018