FERNANDO SCAGLIA to Chromosomes, Human, X
This is a "connection" page, showing publications FERNANDO SCAGLIA has written about Chromosomes, Human, X.
Connection Strength
0.517
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The Xp contiguous deletion syndrome and autism. Am J Med Genet A. 2009 Jun; 149A(6):1138-48.
Score: 0.293
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Attenuated phenotype in a child with trisomy for 1q due to unbalanced X;1 translocation [46,X,der(X),t(X;1)(q28;q32.1)]. Am J Med Genet A. 2004 Jul 01; 128A(1):72-7.
Score: 0.209
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Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males. Genet Med. 2006 Dec; 8(12):784-92.
Score: 0.015