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10. Sex chromosome abnormalities and Noonan Syndrome. Nielsen DB Ariz Med; 1980 Jul; 37(7):486-90. PubMed ID: 7406711 [No Abstract] [Full Text] [Related]
11. Craniosynostosis in the Ullrich-Turner syndrome. Cohen MM Am J Med Genet; 1990 Feb; 35(2):289-90. PubMed ID: 2309772 [No Abstract] [Full Text] [Related]
12. The neurofibromatosis-Noonan syndrome. Mendez HM Am J Med Genet; 1985 Jul; 21(3):471-6. PubMed ID: 3927725 [No Abstract] [Full Text] [Related]
14. Photo essay--Noonan syndrome. Sommer A Am J Med Genet C Semin Med Genet; 2007 Aug; 145C(3):273. PubMed ID: 17640055 [No Abstract] [Full Text] [Related]
15. Noonan-like syndrome mutations in PTPN11 in patients diagnosed with cherubism. Jafarov T; Ferimazova N; Reichenberger E Clin Genet; 2005 Aug; 68(2):190-1. PubMed ID: 15996221 [No Abstract] [Full Text] [Related]
16. [Noonan syndrome in girls]. Kováts-Szabó E Orv Hetil; 1983 Jun; 124(24):1445-7. PubMed ID: 6877825 [No Abstract] [Full Text] [Related]
17. Ullrich-Turner syndrome and neurofibromatosis-1. Schorry EK; Lovell AM; Milatovich A; Saal HM Am J Med Genet; 1996 Dec; 66(4):423-5. PubMed ID: 8989459 [TBL] [Abstract][Full Text] [Related]
18. [Diagnosis and differential diagnosis of Noonan syndrome in a 13-year-old girl]. Krawczyński M; Latos-Bieleńska A; Gabryel-Grudziak A; Baczyk I; Kotwicka W Wiad Lek; 1986 Jul; 39(13):915-21. PubMed ID: 3788154 [No Abstract] [Full Text] [Related]
19. The Noonan syndrome. The Nancy experience revisited. Chery M; Philippe C; Worms AM; Gilgenkrantz S Genet Couns; 1993; 4(2):113-8. PubMed ID: 8357561 [TBL] [Abstract][Full Text] [Related]
20. [The Ullrich-Noonan syndrome in 3 generations]. Franková Y; Stloukalová M; Rubín A Cesk Pediatr; 1986 Oct; 41(10):615-7. PubMed ID: 3502953 [No Abstract] [Full Text] [Related] [Next] [New Search]