Mathews K.,1995

Mathews K., Wang M., Corbit C.K., Godfrey M. Fibrillin (FBN1) mutations in the "neonatal region": towards genotype/phenotype correlations in neonatal Marfan syndrome. - Am.J.Hum.Genet., 1995, v. 57 (suppl.), p. A339.

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Табл. FBN m