210 related articles for article (PubMed ID: 3265306)
1. CFC syndrome: a syndrome distinct from Noonan syndrome.
Verloes A; Le Merrer M; Soyeur D; Kaplan J; Pangalos C; Rigo J; Briard ML
Ann Genet; 1988; 31(4):230-4. PubMed ID: 3265306
[TBL] [Abstract][Full Text] [Related]
2. Cutaneous manifestations in the cardiofaciocutaneous syndrome, a variant of the classical Noonan syndrome. Report of a case and review of the literature.
Weiss G; Confino Y; Shemer A; Trau H
J Eur Acad Dermatol Venereol; 2004 May; 18(3):324-7. PubMed ID: 15096145
[TBL] [Abstract][Full Text] [Related]
3. The Noonan-CFC controversy.
Neri G; Zollino M; Reynolds JF
Am J Med Genet; 1991 Jun; 39(3):367-70. PubMed ID: 1867292
[TBL] [Abstract][Full Text] [Related]
4. The cardio-facio-cutaneous (CFC) syndrome and Noonan syndrome: are they the same?
Fryer AE; Holt PJ; Hughes HE
Am J Med Genet; 1991 Mar; 38(4):548-51. PubMed ID: 2063896
[TBL] [Abstract][Full Text] [Related]
5. [CFC syndrome in mother and daughter: a syndrome distinct from Noonan syndrome].
Blanchet-Bardon C; Puppin D; Fischer R; Dubertret L
Ann Dermatol Venereol; 1991; 118(11):778-80. PubMed ID: 1789629
[No Abstract] [Full Text] [Related]
6. Absence of PTPN11 mutations in 28 cases of cardiofaciocutaneous (CFC) syndrome.
Ion A; Tartaglia M; Song X; Kalidas K; van der Burgt I; Shaw AC; Ming JE; Zampino G; Zackai EH; Dean JC; Somer M; Parenti G; Crosby AH; Patton MA; Gelb BD; Jeffery S
Hum Genet; 2002 Oct; 111(4-5):421-7. PubMed ID: 12384786
[TBL] [Abstract][Full Text] [Related]
7. Fine mapping of Noonan/cardio-facio cutaneous syndrome in a large family.
Legius E; Schollen E; Matthijs G; Fryns JP
Eur J Hum Genet; 1998 Jan; 6(1):32-7. PubMed ID: 9781012
[TBL] [Abstract][Full Text] [Related]
8. The cardiofaciocutaneous syndrome.
Roberts A; Allanson J; Jadico SK; Kavamura MI; Noonan J; Opitz JM; Young T; Neri G
J Med Genet; 2006 Nov; 43(11):833-42. PubMed ID: 16825433
[TBL] [Abstract][Full Text] [Related]
9. [Cardio-facio-cutaneous syndrome--visual diagnosis of a rare syndrome].
Haas K; Schöning M; Enders H
Klin Padiatr; 1994; 206(3):181-3. PubMed ID: 8051913
[TBL] [Abstract][Full Text] [Related]
10. Neurologic and gastrointestinal dysfunction in cardio-facio-cutaneous syndrome: identification of a severe phenotype.
Grebe TA; Clericuzio C
Am J Med Genet; 2000 Nov; 95(2):135-43. PubMed ID: 11078563
[TBL] [Abstract][Full Text] [Related]
11. The CFC syndrome--report of the first two cases outside the United States.
Neri G; Sabatino G; Bertini E; Genuardi M
Am J Med Genet; 1987 Aug; 27(4):767-71. PubMed ID: 3425595
[TBL] [Abstract][Full Text] [Related]
12. [Variability in clinical expression of Noonan syndrome--the report of two familial cases].
Klapecki J; Obersztyn E; Łaniewski-Wołłk M; Szpecht-Potocka A; Mazurczak T
Wiad Lek; 2008; 61(1-3):74-81. PubMed ID: 18717048
[TBL] [Abstract][Full Text] [Related]
13. Skin manifestations of cardio-facio-cutaneous syndrome.
Borradori L; Blanchet-Bardon C
J Am Acad Dermatol; 1993 May; 28(5 Pt 2):815-9. PubMed ID: 8491871
[TBL] [Abstract][Full Text] [Related]
14. A Noonan-like short stature syndrome with sparse hair.
Baraitser M; Patton MA
J Med Genet; 1986 Apr; 23(2):161-4. PubMed ID: 3712393
[TBL] [Abstract][Full Text] [Related]
15. Retinitis pigmentosa in a young man with Noonan syndrome: further evidence that Noonan syndrome (NS) and the cardio-facio-cutaneous syndrome (CFC) are variable manifestations of the same entity?
Lorenzetti ME; Fryns JP
Am J Med Genet; 1996 Oct; 65(2):97-9. PubMed ID: 8911596
[TBL] [Abstract][Full Text] [Related]
16. CFC index for the diagnosis of cardiofaciocutaneous syndrome.
Kavamura MI; Peres CA; Alchorne MM; Brunoni D
Am J Med Genet; 2002 Sep; 112(1):12-6. PubMed ID: 12239713
[TBL] [Abstract][Full Text] [Related]
17. Lumping of CFC and Baraitser-Patton Noonan-like syndromes.
Verloes A; Le Merrer M
Am J Med Genet; 1992 Mar; 42(5):756-7. PubMed ID: 1632454
[No Abstract] [Full Text] [Related]
18. Are cardio-facio-cutaneous syndrome and Noonan syndrome distinct? A case of CFC offspring of a mother with Noonan syndrome.
Leichtman LG
Clin Dysmorphol; 1996 Jan; 5(1):61-4. PubMed ID: 8867661
[TBL] [Abstract][Full Text] [Related]
19. Prolapse of all cardiac valves in Noonan syndrome.
Otikunta AN; Subbareddy YV; Polamuri P; Thakkar A
BMJ Case Rep; 2015 Feb; 2015():. PubMed ID: 25716036
[TBL] [Abstract][Full Text] [Related]
20. PTPN11 mutations are not responsible for the Cardiofaciocutaneous (CFC) syndrome.
Kavamura MI; Pomponi MG; Zollino M; Lecce R; Murdolo M; Brunoni D; Alchorne MM; Opitz JM; Neri G
Eur J Hum Genet; 2003 Jan; 11(1):64-8. PubMed ID: 12529707
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]