These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. A syndrome of mental retardation, short stature, craniofacial anomalies with palpebral ptosis and pulmonary stenosis in three siblings with normal parents. An example of autosomal recessive inheritance of the Noonan phenotype? Maximilian C; Ioan DM; Fryns JP Genet Couns; 1992; 3(2):115-8. PubMed ID: 1642809 [TBL] [Abstract][Full Text] [Related]
4. The cardio-facio-cutaneous (CFC) syndrome: autosomal dominant inheritance in a large family. Fryns JP; Volcke P; Van den Berghe H Genet Couns; 1992; 3(1):19-24. PubMed ID: 1590976 [TBL] [Abstract][Full Text] [Related]
5. Noonan syndrome: a review. Mendez HM; Opitz JM Am J Med Genet; 1985 Jul; 21(3):493-506. PubMed ID: 3895929 [TBL] [Abstract][Full Text] [Related]
6. Mental retardation and Y/8 translocation [karyotype: 46,XY, t(Y;8)(q12;q24)] in father and son. Fryns JP; Kleczkowska A; Dereymaeker AM; Van den Berghe H Helv Paediatr Acta; 1988 Aug; 43(1-2):87-90. PubMed ID: 3170249 [TBL] [Abstract][Full Text] [Related]
8. Acrofacial dysostosis with growth and mental retardation in three males, one with simultaneous Hermansky-Pudlak syndrome. Kelly TE; Cooke RJ; Kester RW Birth Defects Orig Artic Ser; 1977; 13(3B):45-52. PubMed ID: 890099 [No Abstract] [Full Text] [Related]
9. Noonan phenotype in the basal cell nevus syndrome. Grubben C; Fryns JP; Smeets E; Van den Berghe H Genet Couns; 1991; 2(1):47-54. PubMed ID: 1741977 [TBL] [Abstract][Full Text] [Related]
10. Postaxial acrofacial dysostosis syndrome with microcephaly, seizures and profound mental retardation. Hauss-Albert H; Passarge E Am J Med Genet; 1988 Nov; 31(3):701-3. PubMed ID: 3228151 [No Abstract] [Full Text] [Related]
11. Noonan syndrome: the changing phenotype. Allanson JE; Hall JG; Hughes HE; Preus M; Witt RD Am J Med Genet; 1985 Jul; 21(3):507-14. PubMed ID: 4025385 [TBL] [Abstract][Full Text] [Related]
12. Association of hypertelorism and hypospadias--the BBB-syndrome. Michaelis E; Mortier W Helv Paediatr Acta; 1972 Dec; 27(6):575-81. PubMed ID: 4405408 [No Abstract] [Full Text] [Related]
13. Noonan and Klinefelter syndromes in a child. Verloes A; Guidi O; Frederic J; Lambotte C Am J Med Genet; 1987 Jul; 27(3):727-8. PubMed ID: 3631144 [No Abstract] [Full Text] [Related]
14. [Familial and hereditary microcephaly. Study of 10 cases in 4 families]. Bost M; Crouzet G; Jalbert P; Lesage A; Beaudoing A Pediatrie; 1971 Sep; 26(6):587-98. PubMed ID: 5116340 [No Abstract] [Full Text] [Related]
15. Progressive hydrocephalus in two members of a family with autosomal dominant Noonan phenotype. Henn W; Reichert H; Nienhaus H; Zankl M; Lindinger A; Hoffmann W; Zang KD Clin Dysmorphol; 1997 Apr; 6(2):153-6. PubMed ID: 9134296 [TBL] [Abstract][Full Text] [Related]
16. A new familial syndrome with craniofacial abnormalities, osseous defects and mental retardation. Grix A; Blankenship W; Peterson R; Hall B Birth Defects Orig Artic Ser; 1975; 11(5):107-14. PubMed ID: 1218201 [No Abstract] [Full Text] [Related]
17. [Familial Noonan syndrome]. Krüger G; Schumacher K; Mix M; Pelz L Kinderarztl Prax; 1989 May; 57(5):245-8. PubMed ID: 2747123 [TBL] [Abstract][Full Text] [Related]
18. Exclusion of allelism of Noonan syndrome and neurofibromatosis-type 1 in a large family with Noonan syndrome-neurofibromatosis association. Bahuau M; Flintoff W; Assouline B; Lyonnet S; Le Merrer M; Prieur M; Guilloud-Bataille M; Feingold N; Munnich A; Vidaud M; Vidaud D Am J Med Genet; 1996 Dec; 66(3):347-55. PubMed ID: 8985499 [TBL] [Abstract][Full Text] [Related]
19. Acro-fronto-facio-nasal dysostosis: report of a new Brazilian family. Richieri-Costa A; Guion-Almeida ML; Pagnan NA Am J Med Genet; 1992 Dec; 44(6):800-2. PubMed ID: 1481850 [TBL] [Abstract][Full Text] [Related]
20. Constancy of the length of human Y chromosome. Borgaonkar DS; McKusick VA; Herr HM; de los Cobos L; Yoder OC Ann Genet; 1969 Dec; 12(4):262-4. PubMed ID: 5309419 [No Abstract] [Full Text] [Related] [Next] [New Search]