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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 17640055)

  • 1. 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]  

  • 2. [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]  

  • 3. [Noonan syndrome in clinical practice].
    Krajewska-Walasek M
    Pediatr Pol; 1995 Oct; 70(10):809-17. PubMed ID: 8649927
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. [The Saldin-Noonan syndrome].
    Seemanová E; Endler P; Benesová D; Svobodová J; Salichová J
    Cas Lek Cesk; 1978 Aug; 117(31):967-70. PubMed ID: 698998
    [No Abstract]   [Full Text] [Related]  

  • 6. Familial Noonan syndrome.
    Kasturi L; Kulkarni AV; Mashankar VA; Desai UA
    Indian Pediatr; 1995 Mar; 32(3):362-5. PubMed ID: 8613296
    [No Abstract]   [Full Text] [Related]  

  • 7. Neonatal Noonan syndrome with a molluscoid cutaneous excess over the scalp.
    Lacombe D; Taieb A; Masson P; Fayon M; Demarquez JL
    Genet Couns; 1991; 2(4):249-53. PubMed ID: 1799426
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Noonan syndrome. A review.
    Cesur Aydin K; Ozcan I
    Minerva Pediatr; 2008 Jun; 60(3):343-6. PubMed ID: 18487980
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Familial Noonan syndrome].
    Faure Nogueras E; Roche Asensio MJ; Blasco Comenge MC
    Med Clin (Barc); 1983 Feb; 80(5):231-2. PubMed ID: 6855307
    [No Abstract]   [Full Text] [Related]  

  • 10. Time and natural history: the changing face.
    Allanson JE
    J Craniofac Genet Dev Biol; 1989; 9(1):21-8. PubMed ID: 2793999
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Diagnostic usefulness of echocardiography in the Noonan syndrome].
    Velasco-Sánchez RG; Jiménez-Arteaga S; Martínez-Sánchez A; Jiménez-Zepeda D; Alva-Espinoza C; Santamaría-Díaz H; Díaz-Arauzo A
    Bol Med Hosp Infant Mex; 1987 Apr; 44(4):193-201. PubMed ID: 3593514
    [No Abstract]   [Full Text] [Related]  

  • 12. Mutation analysis of the genes involved in the Ras-mitogen-activated protein kinase (MAPK) pathway in Korean patients with Noonan syndrome.
    Lee ST; Ki CS; Lee HJ
    Clin Genet; 2007 Aug; 72(2):150-5. PubMed ID: 17661820
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A new autosomal recessive syndrome with Noonan-like phenotype, myopathy with congenital contractures and malignant hyperthermia.
    Kousseff BG; Nichols P
    Birth Defects Orig Artic Ser; 1985; 21(2):111-7. PubMed ID: 4041573
    [No Abstract]   [Full Text] [Related]  

  • 14. Noonan phenotype with polydactyly.
    Grix A; Hall BD
    Birth Defects Orig Artic Ser; 1979; 15(5B):313-9. PubMed ID: 526585
    [No Abstract]   [Full Text] [Related]  

  • 15. Patient with a neurofibromatosis type 1 mutation but a clinical diagnosis of Noonan syndrome.
    Croonen EA; Yntema HG; van Minkelen R; van den Ouweland AMW; van der Burgt I
    Clin Dysmorphol; 2012 Oct; 21(4):212-214. PubMed ID: 22664660
    [No Abstract]   [Full Text] [Related]  

  • 16. Noonan syndrome. An update and review for the primary pediatrician.
    Noonan JA
    Clin Pediatr (Phila); 1994 Sep; 33(9):548-55. PubMed ID: 8001324
    [No Abstract]   [Full Text] [Related]  

  • 17. [Three recent cases of Noonan's syndrome].
    Vellieux F; Saint-Jacques I; Loubry P; Joly T; Boissière H
    Ann Pediatr (Paris); 1978 Feb; 25(2):91-9. PubMed ID: 16114309
    [No Abstract]   [Full Text] [Related]  

  • 18. Noonan syndrome.
    Allanson JE
    Am J Med Genet C Semin Med Genet; 2007 Aug; 145C(3):274-9. PubMed ID: 17639592
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Noonan syndrome: a clinical description emphasizing the cardiac findings.
    Noonan J; O'Connor W
    Acta Paediatr Jpn; 1996 Feb; 38(1):76-83. PubMed ID: 8992867
    [No Abstract]   [Full Text] [Related]  

  • 20. Sex chromosome abnormalities and Noonan Syndrome.
    Nielsen DB
    Ariz Med; 1980 Jul; 37(7):486-90. PubMed ID: 7406711
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.