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5. [Turner's phenotype and diagnosis of Noonan's syndrome]. Latini G, Berardi R. Pediatr Med Chir; 1982 Mar; 4(5):535-8. PubMed ID: 6927352 [Abstract] [Full Text] [Related]
6. [The C heterochromatin of chromosomes 1, 9, 16 and Y in patients with Noonan's syndrome]. Podugol'nikova OA, Solonichenko VG. Tsitol Genet; 1994 Mar; 28(3):85-8. PubMed ID: 7974791 [Abstract] [Full Text] [Related]
7. Dilated cardiomyopathy in Noonan's syndrome: a first autopsy case. Kurose A, Oyama K, Murakami Y, Ohyama K, Segawa I, Sawai T. Hum Pathol; 2000 Jun; 31(6):764-7. PubMed ID: 10872673 [Abstract] [Full Text] [Related]
9. Noonan's syndrome. Agarwal B, Guha D, Banerjee D. J Indian Med Assoc; 1999 Dec; 97(12):524. PubMed ID: 10638133 [No Abstract] [Full Text] [Related]
10. Bilateral multiple pulmonary arteriovenous fistulas and duplicated renal collecting system in a child with Noonan's syndrome. Semizel E, Bostan OM, Saglam H. Cardiol Young; 2007 Apr; 17(2):229-31. PubMed ID: 17319980 [Abstract] [Full Text] [Related]
11. [Rare clinicogenetic case of Noonan's syndrome]. Goranov M, Nacheva M, Simeonova M, Arnaudova M. Akush Ginekol (Sofiia); 1981 Apr; 20(5):414-7. PubMed ID: 7325335 [No Abstract] [Full Text] [Related]
12. [Somatometric profile of female patients with Turner's syndrome and male and female patients with Noonan's syndrome]. Guízar-Vázquez JJ, Ramírez-Gutiérrez V, Sánchez-Aguilar G, Salamanca-Gómez F. Bol Med Hosp Infant Mex; 1983 Jul; 40(7):367-71. PubMed ID: 6626306 [No Abstract] [Full Text] [Related]