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 *

78 related articles for article (PubMed ID: 120582)

  • 41. The acrofacial dysostoses--a wide spectrum of overlapping phenotypes.
    Dimitrov B; Balikova I; Bradinova I; Zahariev D; Popova A; Simeonov E; De Smet L; Devriendt K; Fryns JP
    Genet Couns; 2005; 16(2):181-6. PubMed ID: 16080300
    [No Abstract]   [Full Text] [Related]  

  • 42. [Sex-linked inheritance in fronto-metaphyseal dysplasia].
    Balestrazzi P
    J Genet Hum; 1985 Dec; 33(5):419-25. PubMed ID: 4093771
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Skeletal dysplasia with brachytelephalangy in a patient with a congenital disorder of glycosylation due to ALG6 gene mutations.
    Drijvers JM; Lefeber DJ; de Munnik SA; Pfundt R; van de Leeuw N; Marcelis C; Thiel C; Koerner C; Wevers RA; Morava E
    Clin Genet; 2010 May; 77(5):507-9. PubMed ID: 20447155
    [No Abstract]   [Full Text] [Related]  

  • 44. [Marie-Sainton syndrome (cleidocranial dysostosis) associated with osseous changes in the hand].
    Krawczyński M; Stańska M; Cichy W; Socha J
    Endokrynol Pol; 1975; 26(2):133-8. PubMed ID: 1132375
    [No Abstract]   [Full Text] [Related]  

  • 45. Hearing loss due to cranio-metaphysial dysplasia.
    Morgan DW; Aldren C; Hoare TJ
    J Laryngol Otol; 1990 Oct; 104(10):807-8. PubMed ID: 2246582
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Glaucoma in oculo-dento-osseous dysplasia.
    Traboulsi EI; Parks MM
    Am J Ophthalmol; 1990 Mar; 109(3):310-3. PubMed ID: 2309863
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Unusual complex of congenital malformations.
    Zolotukhina T; Kuznetsov M; Lurie I; Ilyina H
    Am J Med Genet; 1993 Jul; 46(6):728-9. PubMed ID: 8362920
    [No Abstract]   [Full Text] [Related]  

  • 48. [Skull and tooth abnormalities in a patient with osteopathia striata].
    De Boer SM; Van Gool AV
    Ned Tijdschr Geneeskd; 1974 Sep; 118(36):1373-80. PubMed ID: 4410894
    [No Abstract]   [Full Text] [Related]  

  • 49. Clones with 5q - and inversion of chromosome 7 in PHA stimulated peripheral blood.
    Leeksma CH; den Nijs J; Havik F; Kerkhofs H; Geraedts JP
    Scand J Haematol; 1981 Jul; 27(1):19-24. PubMed ID: 7199756
    [No Abstract]   [Full Text] [Related]  

  • 50. Familial metaphyseal dysplasia.
    Rimoin DL
    Lancet; 1970 Aug; 2(7667):309-10. PubMed ID: 4194380
    [No Abstract]   [Full Text] [Related]  

  • 51. [Crossed congenital hemihypertrophy in benign unilateral nephromegaly].
    Sbihi A; Hamdouch M; Iraqi-Hamdouch N; Outarahout O; Benhamou M; Alami TH
    Maghrib Tibbi; 1980 Oct; 2(3):255-63. PubMed ID: 7230887
    [No Abstract]   [Full Text] [Related]  

  • 52. Acromicric Dysplasia Caused by a Novel Heterozygous Mutation of FBN1 and Effects of Growth Hormone Treatment.
    Jin HS; Song HY; Cho SY; Ki CS; Yang SH; Kim OH; Kim SJ
    Ann Lab Med; 2017 Jan; 37(1):92-94. PubMed ID: 27834076
    [No Abstract]   [Full Text] [Related]  

  • 53. [Osteo-vascular associated dysplasias. Rarity of phleboectasic osteohypoplastic forms].
    Zelli GP; Pontone P; Iavicoli N
    Ann Ital Chir; 1975-1976; 49(1-6):141-9. PubMed ID: 1053133
    [No Abstract]   [Full Text] [Related]  

  • 54. A Rare Cause of Recurrent Stroke in a Visually Impaired 10-year-old Girl.
    Chindanuru S; Paulpandian R; Srinivasan T; Chandrasekaran V; Jagadisan B; Biswal N; Chakkalakkoombil SV; Ananthakrishnan R
    Indian J Pediatr; 2017 Feb; 84(2):160-161. PubMed ID: 27638652
    [No Abstract]   [Full Text] [Related]  

  • 55. Geleophysic dysplasia: a novel in-frame deletion of a tandem repeat in the ADAMTSL2 gene.
    García-Ortiz L; Gutiérrez-Salinas J; Del Carmen Chima Galán M; García RL; de la Concepción A Yerena M
    Am J Med Genet A; 2015 Aug; 167A(8):1949-51. PubMed ID: 25850559
    [No Abstract]   [Full Text] [Related]  

  • 56. Idiopathic thrombocytopenic purpura with X chromosome abnormality.
    Murayama T; Ito M; Imoto S; Matsushita K; Matozaki S; Nakagawa T; Nakao Y
    Am J Hematol; 1993 Feb; 42(2):239-40. PubMed ID: 8438896
    [No Abstract]   [Full Text] [Related]  

  • 57. Familial metaphyseal dysplasia.
    Gladney JH; Monteleone PL
    Lancet; 1970 Jul; 2(7662):44-5. PubMed ID: 4194833
    [No Abstract]   [Full Text] [Related]  

  • 58. Brief report. Embryonic arterial and skeletal dysgenesis: Syracuse colloquium on congenital arterial and skeletal birth defects September 28 and 29, 2013.
    Hootnick D
    Birth Defects Res A Clin Mol Teratol; 2014 Oct; 100(10):789-91. PubMed ID: 24863888
    [No Abstract]   [Full Text] [Related]  

  • 59. [Pyle-Cohn's cranio-metaphyseal dysplasia].
    Siliquini PL
    Minerva Ortop; 1967 Mar; 18(3):129-33. PubMed ID: 5605890
    [No Abstract]   [Full Text] [Related]  

  • 60. [Congenital myasthenia associated with skeletal abnormalities and cataract in two sisters].
    Okabe I; Kobayashi S; Kamoshita S
    No To Hattatsu; 1985 May; 17(3):245-50. PubMed ID: 4015893
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.