BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

178 related articles for article (PubMed ID: 9415478)

  • 41. Atypical manifestations of two cases of trisomy 9 syndrome: rethinking development delay.
    Saneto RP; Applegate KE; Frankel DG
    Am J Med Genet; 1998 Oct; 80(1):42-5. PubMed ID: 9800910
    [TBL] [Abstract][Full Text] [Related]  

  • 42. 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]  

  • 43. Frank-ter Haar syndrome with unusual clinical features.
    Dundar M; Saatci C; Tasdemir S; Akcakus M; Caglayan AO; Ozkul Y
    Eur J Med Genet; 2009; 52(4):247-9. PubMed ID: 19303467
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Autosomal recessive syndrome of sacral and conotruncal developmental field defects (Kousseff syndrome).
    Toriello HV; Sharda JK; Beaumont EJ
    Am J Med Genet; 1985 Oct; 22(2):357-60. PubMed ID: 4050868
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [Amniotic disease in the mother and severe heart abnormalities in 2 infants].
    Canki N
    J Genet Hum; 1985 Jan; 33(1):37-44. PubMed ID: 3981140
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Acro-renal-mandibular syndrome.
    Halal F; Desgranges MF; Leduc B; Thêorét G; Bettez P
    Am J Med Genet; 1980; 5(3):277-84. PubMed ID: 7405959
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Váradi syndrome (OFD VI) or Opitz trigonocephaly syndrome: overlapping manifestations in two cousins.
    Cleper R; Kauschansky A; Varsano I; Frydman M
    Am J Med Genet; 1993 Sep; 47(4):451-5. PubMed ID: 8256802
    [TBL] [Abstract][Full Text] [Related]  

  • 48. [The Freeman-Sheldon syndrome with mental retardation].
    Cirillo Silengo M; Davi GF; Bianco R; De Marco A; Costa M; Franceschini P; Bonenti G
    Minerva Pediatr; 1982 Mar; 34(6):277-80. PubMed ID: 6808331
    [No Abstract]   [Full Text] [Related]  

  • 49. Yunis-Varon syndrome.
    Bhatia S; Holla RG
    Indian Pediatr; 2005 Apr; 42(4):373-5. PubMed ID: 15876600
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Carpenter syndrome with normal intelligence: Brazilian girl born to consanguineous parents.
    Richieri-Costa A; Pirolo Júnior L; Cohen MM
    Am J Med Genet; 1993 Aug; 47(2):281-3. PubMed ID: 8213921
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Cutis laxa in Kabuki make-up syndrome.
    Vaccaro M; Salpietro DC; Briuglia S; Merlino MV; Guarneri F; Dallapiccola B
    J Am Acad Dermatol; 2005 Nov; 53(5 Suppl 1):S247-51. PubMed ID: 16227101
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Apparent Lenz microphthalmia syndrome: a patient with unusual manifestations.
    Okumus N; Zenciroglu A; Demirel N; Bas AY; Ceylaner S
    Genet Couns; 2008; 19(2):177-82. PubMed ID: 18618992
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Acro-oto-ocular syndrome: further evidence for a new autosomal recessive disorder.
    Bertola DR; Wolf LM; Toriello HV; Netzloff ML
    Am J Med Genet; 1997 Dec; 73(4):442-6. PubMed ID: 9415472
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Unusual association of congenital malformations: craniosynostosis, heart defect, abnormal intestinal innervation and urogenital abnormalities.
    Van Nesselrooij BP; Spliet W; Beemer FA
    Clin Dysmorphol; 1998 Jan; 7(1):51-3. PubMed ID: 9546831
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Severe cardiac anomalies in sibs with Larsen syndrome.
    Strisciuglio P; Sebastio G; Andria G; Maione S; Raia V
    J Med Genet; 1983 Dec; 20(6):422-4. PubMed ID: 6655668
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Autosomal recessive syndrome of growth and mental retardation, seizures, retinal abnormalities, and osteodysplasia with similarity to the Gurrieri syndrome.
    Orrico A; Hayek G; Burroni L
    Am J Med Genet; 1999 Jan; 82(1):84-7. PubMed ID: 9916849
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Shprintzen-Goldberg syndrome associated with a novel missense mutation in TGFBR2.
    van Steensel MA; van Geel M; Parren LJ; Schrander-Stumpel CT; Marcus-Soekarman D
    Exp Dermatol; 2008 Apr; 17(4):362-5. PubMed ID: 17979970
    [TBL] [Abstract][Full Text] [Related]  

  • 58. De novo partial duplications 1p: report of two new cases and review.
    Garcia-Heras J; Corley N; Garcia MF; Kukolich MK; Smith KG; Day DW
    Am J Med Genet; 1999 Jan; 82(3):261-4. PubMed ID: 10215552
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Carpenter syndrome: natural history and clinical spectrum.
    Robinson LK; James HE; Mubarak SJ; Allen EJ; Jones KL
    Am J Med Genet; 1985 Mar; 20(3):461-9. PubMed ID: 3993675
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review.
    Leonardi ML; Pai GS; Wilkes B; Lebel RR
    Am J Med Genet; 2001 Aug; 102(3):237-42. PubMed ID: 11484200
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.