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 *

105 related articles for article (PubMed ID: 7558058)

  • 41. SC phocomelia syndrome, premature centromere separation, and congenital cranial nerve paralysis in two sisters, one with malignant melanoma.
    Parry DM; Mulvihill JJ; Tsai SE; Kaiser-Kupfer MI; Cowan JM
    Am J Med Genet; 1986 Aug; 24(4):653-72. PubMed ID: 3740099
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Neurocognitive profile of a young adolescent with DK phocomelia/von Voss phocomelia/von Voss Cherstvoy syndrome.
    Antonini TN; Van Horn Kerne V; Axelrad ME; Karaviti LP; Schwartz DD
    Am J Med Genet A; 2015 Jul; 167(7):1632-6. PubMed ID: 25899150
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Chromatid repulsion associated with Roberts/SC phocomelia syndrome is reduced in malignant cells and not expressed in interspecies somatic-cell hybrids.
    Krassikoff NE; Cowan JM; Parry DM; Francke U
    Am J Hum Genet; 1986 Nov; 39(5):618-30. PubMed ID: 3788975
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Holt-Oram syndrome].
    Kullmann F; Grimm T
    Dtsch Med Wochenschr; 1993 Oct; 118(40):1455-62. PubMed ID: 8404501
    [No Abstract]   [Full Text] [Related]  

  • 45. Expanding the mutation and clinical spectrum of Roberts syndrome.
    Afifi HH; Abdel-Salam GM; Eid MM; Tosson AM; Shousha WG; Abdel Azeem AA; Farag MK; Mehrez MI; Gaber KR
    Congenit Anom (Kyoto); 2016 Jul; 56(4):154-62. PubMed ID: 26710928
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [Genetic morphological fatal syndromes. The Fryns syndrome].
    Henkel KE; Pfeiffer RA; Stöss H
    Pathologe; 1993 Mar; 14(2):92-3. PubMed ID: 8469652
    [No Abstract]   [Full Text] [Related]  

  • 47. Pseudo-Roberts Syndrome: An Entity or Not?
    Salari B; Dehner LP
    Fetal Pediatr Pathol; 2022 Jun; 41(3):396-402. PubMed ID: 33026893
    [No Abstract]   [Full Text] [Related]  

  • 48. Limb/pelvis/uterus-hypoplasia/aplasia syndrome.
    Teebi AS
    J Med Genet; 1993 Sep; 30(9):797. PubMed ID: 8411080
    [No Abstract]   [Full Text] [Related]  

  • 49. [Roberts-SC phocomelia syndrome].
    Baggio P; Danda R; Audino G
    Pediatr Med Chir; 1986; 8(1):115-9. PubMed ID: 3725603
    [TBL] [Abstract][Full Text] [Related]  

  • 50. A case of SC-phocomelia syndrome with nonrandom centromere separation.
    Bökesoy I; Balci S; Bilgiç S
    Prog Clin Biol Res; 1982; 104():351-8. PubMed ID: 7163280
    [No Abstract]   [Full Text] [Related]  

  • 51. Tetra-amelia and lung aplasia syndrome: report of a new family and exclusion of candidate genes.
    Krahn M; Julia S; Sigaudy S; Liprandi A; Bernard R; Gonnet K; Heuertz S; Bonaventure J; Chau C; Fredouille C; Levy N; Philip N
    Clin Genet; 2005 Dec; 68(6):558-60. PubMed ID: 16283889
    [No Abstract]   [Full Text] [Related]  

  • 52. A sibship with the pseudothalidomide syndrome and an association with Rh incompatibility.
    Judge C
    Med J Aust; 1973 Aug; 2(6):280-1. PubMed ID: 4795547
    [No Abstract]   [Full Text] [Related]  

  • 53. Zimmer phocomelia: delineation by principal coordinate analysis.
    Kosaki K; Jones MC; Stayboldt C
    Am J Med Genet; 1996 Dec; 66(1):55-9. PubMed ID: 8957512
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [3 consecutive deliveries of infants of young parents with tetraphocomelia of the Robert's type].
    Zergollern L; Hitrec V; Cajkovac V; Banić I; Kovacević S
    Lijec Vjesn; 1975 Oct; 97(9):519-22. PubMed ID: 1223582
    [No Abstract]   [Full Text] [Related]  

  • 55. Robinow syndrome.
    Singh SK; Bhadada SK; Singh R; Sinha SK; Singh SK; Agrawal JK
    J Assoc Physicians India; 2000 Aug; 48(8):836-7. PubMed ID: 11273483
    [TBL] [Abstract][Full Text] [Related]  

  • 56. "Isolated" radial ray defect may be due to Rothmund-Thomson syndrome.
    Moss C; Bacon CJ; Mueller RF
    Clin Genet; 1990 Oct; 38(4):318-9. PubMed ID: 2268978
    [No Abstract]   [Full Text] [Related]  

  • 57. History of C-patient with SC-Roberts/pseudothalidamide syndrome.
    Feingold M
    Am J Med Genet; 1992 Jul; 43(5):898-9. PubMed ID: 1642282
    [No Abstract]   [Full Text] [Related]  

  • 58. Jancar syndrome: mental retardation, spasticity, and distal transverse limbs defects.
    Zlotogora J; Glick B
    Am J Med Genet; 1993 Aug; 47(1):89-90. PubMed ID: 8368260
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Tetraphocomelia in the syndrome of thrombocytopenia with absent radii (TAR syndrome).
    Anyane-Yeboa K; Jaramillo S; Nagel C; Grebin B
    Am J Med Genet; 1985 Apr; 20(4):571-6. PubMed ID: 3993682
    [TBL] [Abstract][Full Text] [Related]  

  • 60. DK phocomelia phenotype (von Voss-Cherstvoy syndrome) caused by somatic mosaicism for del(13q).
    Bamforth JS; Lin CC
    Am J Med Genet; 1997 Dec; 73(4):408-11. PubMed ID: 9415466
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.