MOISE LEVY to Mutation
This is a "connection" page, showing publications MOISE LEVY has written about Mutation.
Connection Strength
0.207
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Adams-Oliver Syndrome Type 2 in Association with Compound Heterozygous DOCK6 Mutations. Pediatr Dermatol. 2017 Sep; 34(5):e249-e253.
Score: 0.050
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Epidermolysis Bullosa with Pyloric Atresia and Significant Urologic Involvement. Pediatr Dermatol. 2017 Jan; 34(1):e61-e64.
Score: 0.048
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Self-healing collodion membrane and mild nonbullous congenital ichthyosiform erythroderma due to 2 novel mutations in the ALOX12B gene. Arch Dermatol. 2008 Mar; 144(3):351-6.
Score: 0.026
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Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndrome. J Natl Cancer Inst. 2003 May 07; 95(9):669-74.
Score: 0.019
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Intron-size constraint as a mutational mechanism in Rothmund-Thomson syndrome. Am J Hum Genet. 2002 Jul; 71(1):165-7.
Score: 0.017
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Hyper-immunoglobulin D syndrome with novel mutations in an afebrile infant. Pediatr Dermatol. 2018 Jul; 35(4):482-485.
Score: 0.013
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Differentiating skin-limited and multisystem Langerhans cell histiocytosis. J Pediatr. 2014 Nov; 165(5):990-6.
Score: 0.010
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Multilineage somatic activating mutations in HRAS and NRAS cause mosaic cutaneous and skeletal lesions, elevated FGF23 and hypophosphatemia. Hum Mol Genet. 2014 Jan 15; 23(2):397-407.
Score: 0.010
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Metastatic squamous cell carcinoma of the oropharynx in a child with a mutation in the Connexin 26 gene. J Pediatr Hematol Oncol. 2011 Jul; 33(5):387-9.
Score: 0.008
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Incontinentia pigmenti in male patients. J Am Acad Dermatol. 2006 Aug; 55(2):251-5.
Score: 0.006