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6. [Hypertrophic cardiomyopathy associated with Noonan's syndrome and membranous aortic subvalvular stenosis associated with Turner's syndrome. Report of 2 clinical cases]. Perrotta Scaravilli E; Pontillo D; Pennacchia F; Boccanelli A; Greco C; Lo Schiavo P G Ital Cardiol; 1987 Sep; 17(9):800-6. PubMed ID: 3692082 [TBL] [Abstract][Full Text] [Related]
7. Turner's phenotype in the male. Ferrier PE; Ferrier SA Pediatrics; 1967 Oct; 40(4):575-85. PubMed ID: 6051057 [No Abstract] [Full Text] [Related]
8. [Noonan's syndrome. Genetic and cardiological study of 2 cases]. Saint-Rome G; Davignon A; Kratz C Union Med Can; 1970 Sep; 99(9):1602-12. PubMed ID: 5005748 [No Abstract] [Full Text] [Related]
9. [Turner's phenotype and diagnosis of Noonan's syndrome]. Latini G; Berardi R Pediatr Med Chir; 1982; 4(5):535-8. PubMed ID: 6927352 [TBL] [Abstract][Full Text] [Related]
10. [Palmar and plantar dermatoglyphics in Turner's syndrome]. Gebala A; Dobrzańska A; Grzeszyk C Pediatr Pol; 1970 Mar; 45(3):275-84. PubMed ID: 5441588 [No Abstract] [Full Text] [Related]
11. Noonan's syndrome (XX and XY Turner phenotype) in three generations of a family. Baird PA; De Jong BP J Pediatr; 1972 Jan; 80(1):110-4. PubMed ID: 5016336 [No Abstract] [Full Text] [Related]
13. [3 recent cases of Noonan's syndrome]. Vellieux F; Saint-Jacques I; Loubry P; Joly T; Boissière H Sem Hop; 1978 Mar; 54(5-8):335-43. PubMed ID: 211629 [TBL] [Abstract][Full Text] [Related]
14. Turner's syndrome in one of monozygotic twins with mosaicism. Potter AM; Taitz LS Acta Paediatr Scand; 1972 Jul; 61(4):473-6. PubMed ID: 5041395 [No Abstract] [Full Text] [Related]
15. A double chromosomal aberration of the 47, XX, 21+-47, XXp-q-, 21+ type in a girl with features of Down's and Turner's syndromes. Mikel'saar AV; Blyumina MG; Kuznetsova LI; Mikel'saar RV; Lur'e IV Sov Genet; 1971 May; 7(5):675-9. PubMed ID: 4272425 [No Abstract] [Full Text] [Related]
17. [Translocation D-D and Turner's syndrome. Considerations on a rare association of chromosome pathology]. Giovannucci ML; Pierro U; Cordelli F; Paoli A Haematologica; 1969; 54(11):813-26. PubMed ID: 4993250 [No Abstract] [Full Text] [Related]
18. [Electroencephalographic study of Turner's syndrome]. Poenaru S; Stanesco V; Poenaru L; Stoian D Acta Neurol Belg; 1970; 70(5):509-22. PubMed ID: 4996762 [No Abstract] [Full Text] [Related]
19. [Anomalies in dermatoglyphics in Turner's syndrome and Klinefelter's syndrome (study based on 25 cases of personal observation)]. Faggiano M; Minozzi M; Salerno M; Lombardi G; Nunziata V Folia Endocrinol; 1972 Feb; 25(1):69-82. PubMed ID: 5067412 [No Abstract] [Full Text] [Related]
20. Turner's syndrome: cytogenetic study of a patient included in the initial report of Turner. Sparkes RS; Kolodny S J Clin Endocrinol Metab; 1966 May; 26(5):577-9. PubMed ID: 5938373 [No Abstract] [Full Text] [Related] [Next] [New Search]