BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

233 related articles for article (PubMed ID: 11057188)

  • 1. [FG syndrome].
    Kato R
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):182-3. PubMed ID: 11057188
    [No Abstract]   [Full Text] [Related]  

  • 2. [Coffin-Lowry syndrome].
    Ishii T
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):163-5. PubMed ID: 11057180
    [No Abstract]   [Full Text] [Related]  

  • 3. [Seckel syndrome].
    Yokoyama Y
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):246-7. PubMed ID: 11057215
    [No Abstract]   [Full Text] [Related]  

  • 4. Possible new autosomal recessive syndrome of partial agenesis of the corpus callosum, pontine hypoplasia, focal white matter changes, hypotonia, mental retardation, and minor anomalies.
    Jonas RE; Kimonis VE; Morales A
    Am J Med Genet; 1997 Dec; 73(2):184-8. PubMed ID: 9409870
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Sensorineural deafness in the FG syndrome: report on four new cases.
    Neri G; Blumberg B; Miles PV; Opitz JM
    Am J Med Genet; 1984 Oct; 19(2):369-77. PubMed ID: 6542310
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Marden-Walker syndrome].
    Imaizumi K
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):15-7. PubMed ID: 11057127
    [No Abstract]   [Full Text] [Related]  

  • 7. The FG syndrome: further characterization, report of a third family, and of a sporadic case.
    Riccardi VM; Hässler E; Lubinsky MS
    Am J Med Genet; 1977; 1(1):47-58. PubMed ID: 565138
    [TBL] [Abstract][Full Text] [Related]  

  • 8. FG syndrome: report of three new families with linkage to Xq12-q22.1.
    Graham JM; Tackels D; Dibbern K; Superneau D; Rogers C; Corning K; Schwartz CE
    Am J Med Genet; 1998 Nov; 80(2):145-56. PubMed ID: 9805132
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [9p-syndrome].
    Fujita H
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):318-9. PubMed ID: 11057244
    [No Abstract]   [Full Text] [Related]  

  • 10. [Marden-Walker syndrome].
    Kurotaki N; Niikawa N
    Ryoikibetsu Shokogun Shirizu; 2001; (36):479-80. PubMed ID: 11596443
    [No Abstract]   [Full Text] [Related]  

  • 11. FG syndrome in a premature male.
    Bianchi DW
    Am J Med Genet; 1984 Oct; 19(2):383-6. PubMed ID: 6507484
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical and behavioral characteristics in FG syndrome.
    Graham JM; Superneau D; Rogers RC; Corning K; Schwartz CE; Dykens EM
    Am J Med Genet; 1999 Aug; 85(5):470-5. PubMed ID: 10405444
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [4p deletion syndrome].
    Narahara K
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):309-11. PubMed ID: 11057240
    [No Abstract]   [Full Text] [Related]  

  • 14. [Partial trisomy 10q syndrome].
    Imaizumi K
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):325-6. PubMed ID: 11057247
    [No Abstract]   [Full Text] [Related]  

  • 15. [Trisomy 8 mosaic syndrome].
    Hada S; Abe T
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):316-7. PubMed ID: 11057243
    [No Abstract]   [Full Text] [Related]  

  • 16. FG syndrome: the trias mental retardation, hypotonia and constipation reviewed.
    Zwamborn-Hanssen AM; Schrander-Stumpel CT; Smeets E; Decock P; Fryns JP
    Genet Couns; 1995; 6(4):313-9. PubMed ID: 8775418
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Cohen syndrome].
    Kayashima T; Niikawa N
    Ryoikibetsu Shokogun Shirizu; 2001; (36):477-8. PubMed ID: 11596442
    [No Abstract]   [Full Text] [Related]  

  • 18. [Weaver syndrome].
    Tsukahara M; Tsujino K
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):258-9. PubMed ID: 11057220
    [No Abstract]   [Full Text] [Related]  

  • 19. X-linked syndrome of mental retardation, short stature, and hypertelorism: a new syndrome or a further example of the FG syndrome?
    Bottani A
    Am J Med Genet; 1994 May; 51(1):87-8. PubMed ID: 8030678
    [No Abstract]   [Full Text] [Related]  

  • 20. Malpuech syndrome: a possible relationship with the Wolf-Hirschhorn/Pitt-Roger-Danks phenotype.
    Selicorni A; Faravelli F
    Am J Med Genet; 2000 Nov; 95(3):291. PubMed ID: 11102941
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 12.