JULIE GASTIER-FOSTER to Syndrome
This is a "connection" page, showing publications JULIE GASTIER-FOSTER has written about Syndrome.
Connection Strength
0.229
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12q14 microdeletion associated with HMGA2 gene disruption and growth restriction. Am J Med Genet A. 2012 Nov; 158A(11):2925-30.
Score: 0.084
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Diverse deletions in the growth hormone receptor gene cause growth hormone insensitivity syndrome. Hum Mutat. 2000 Oct; 16(4):323-33.
Score: 0.037
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MCPH1 deletion in a newborn with severe microcephaly and premature chromosome condensation. Eur J Med Genet. 2013 Nov; 56(11):609-13.
Score: 0.023
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Multigeneration family with short stature, developmental delay, and dysmorphic features due to 4q27-q28.1 microdeletion. Eur J Med Genet. 2013 Sep; 56(9):521-5.
Score: 0.022
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Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus. Am J Hum Genet. 2013 Feb 07; 92(2):210-20.
Score: 0.021
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Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorder. Am J Hum Genet. 2011 Oct 07; 89(4):551-63.
Score: 0.020
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Identification of a recurrent microdeletion at 17q23.1q23.2 flanked by segmental duplications associated with heart defects and limb abnormalities. Am J Hum Genet. 2010 Mar 12; 86(3):454-61.
Score: 0.018
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Traces of her workings. Nat Genet. 1992 Sep; 2(1):5-8.
Score: 0.005