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.
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.
