FERNANDO SCAGLIA to Infant, Newborn, Diseases
This is a "connection" page, showing publications FERNANDO SCAGLIA has written about Infant, Newborn, Diseases.
Connection Strength
0.198
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Complex Compound Inheritance of Lethal Lung Developmental Disorders Due to Disruption of the TBX-FGF Pathway. Am J Hum Genet. 2019 02 07; 104(2):213-228.
Score: 0.129
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Maternal systemic primary carnitine deficiency uncovered by newborn screening: clinical, biochemical, and molecular aspects. Genet Med. 2010 Jan; 12(1):19-24.
Score: 0.069