BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

233 related articles for article (PubMed ID: 11057188)

  • 21. A gene for FG syndrome maps in the Xq12-q21.31 region.
    Briault S; Hill R; Shrimpton A; Zhu D; Till M; Ronce N; Margaritte-Jeannin P; Baraitser M; Middleton-Price H; Malcolm S; Thompson E; Hoo J; Wilson G; Romano C; Guichet A; Pembrey M; Fontes M; Poustka A; Moraine C
    Am J Med Genet; 1997 Nov; 73(1):87-90. PubMed ID: 9375929
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [FG syndrome].
    Kato R
    Ryoikibetsu Shokogun Shirizu; 2001; (33):710-1. PubMed ID: 11462647
    [No Abstract]   [Full Text] [Related]  

  • 23. Microcephaly and digital anomalies: a newly recognized syndrome of recessively inherited mental retardation.
    Kelly TE; Kirson L; Wyatt J
    Am J Med Genet; 1993 Feb; 45(3):353-5. PubMed ID: 8434622
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Cohen syndrome].
    Kondo I
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):10-1. PubMed ID: 11057125
    [No Abstract]   [Full Text] [Related]  

  • 25. Manifestations in four males with and an obligate carrier of the Lenz microphthalmia syndrome.
    Forrester S; Kovach MJ; Reynolds NM; Urban R; Kimonis V
    Am J Med Genet; 2001 Jan; 98(1):92-100. PubMed ID: 11426460
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Neu-Laxova syndrome].
    Oho Y; Okuyama T
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):21-2. PubMed ID: 11057129
    [No Abstract]   [Full Text] [Related]  

  • 27. Polyhydramnios and paroxysmal atrial tachycardia as first clinical signs in Costello syndrome.
    Fryns JP; Devlieger H; Gewillig M; Lukusa P; Devriendt K
    Genet Couns; 1996; 7(3):237-9. PubMed ID: 8897048
    [No Abstract]   [Full Text] [Related]  

  • 28. [Cat eye syndrome].
    Teraoka M; Narahara K
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):348-9. PubMed ID: 11057256
    [No Abstract]   [Full Text] [Related]  

  • 29. Splitting and lumping in the nosology of XLMR.
    Stevenson RE
    Am J Med Genet; 2000; 97(3):174-82. PubMed ID: 11449485
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Japanese kindred with FG syndrome.
    Kato R; Niikawa N; Nagai T; Fukushima Y
    Am J Med Genet; 1994 Aug; 52(2):242-3. PubMed ID: 7802020
    [No Abstract]   [Full Text] [Related]  

  • 31. Refined gene localization for the Miles-Carpenter syndrome (MCS).
    Tackels D; Schwartz CE; Carpenter NJ; Miles JH
    Am J Med Genet; 1999 Jul; 85(3):221-2. PubMed ID: 10398232
    [No Abstract]   [Full Text] [Related]  

  • 32. The FG syndrome from a pathological perspective.
    Neri C; Moser K; Pysher TJ; Boettger DR; Neri G; Opitz JM
    Fetal Pediatr Pathol; 2011; 30(2):71-6. PubMed ID: 21391746
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Expansion of the phenotype in Hennekam syndrome: a case with new manifestations.
    Angle B; Hersh JH
    Am J Med Genet; 1997 Aug; 71(2):211-4. PubMed ID: 9217224
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Kabuki make-up syndrome].
    Kuroki Y
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):272-3. PubMed ID: 11057225
    [No Abstract]   [Full Text] [Related]  

  • 35. Genetic heterogeneity of syndromic X-linked recessive microphthalmia-anophthalmia: is Lenz microphthalmia a single disorder?
    Ng D; Hadley DW; Tifft CJ; Biesecker LG
    Am J Med Genet; 2002 Jul; 110(4):308-14. PubMed ID: 12116202
    [TBL] [Abstract][Full Text] [Related]  

  • 36. MED12 missense mutation in a three-generation family. Clinical characterization of MED12-related disorders and literature review.
    Rubinato E; Rondeau S; Giuliano F; Kossorotoff M; Parodi M; Gherbi S; Steffan J; Jonard L; Marlin S
    Eur J Med Genet; 2020 Mar; 63(3):103768. PubMed ID: 31536828
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Ruvalcaba syndrome].
    Ishii T
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):244-5. PubMed ID: 11057214
    [No Abstract]   [Full Text] [Related]  

  • 38. Prenatal diagnosis in Coffin-Lowry syndrome demonstrates germinal mosaicism confirmed by mutation analysis.
    Horn D; Delaunoy JP; Kunze J
    Prenat Diagn; 2001 Oct; 21(10):881-4. PubMed ID: 11746134
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Schinzel-Giedion syndrome].
    Okamoto N
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):35-7. PubMed ID: 11057134
    [No Abstract]   [Full Text] [Related]  

  • 40. [Triploidy syndrome and diploid/triploid mixoploidy syndrome].
    Kato R
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):361-2. PubMed ID: 11057261
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.