BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

149 related articles for article (PubMed ID: 1255317)

  • 1. A new syndrome of mental deficiency with craniofacial, limb, and anal abnormalities.
    Keller MA; Jones KL; Nyhan WL; Francke U; Dixson B
    J Pediatr; 1976 Apr; 88(4 Pt 1):589-91. PubMed ID: 1255317
    [No Abstract]   [Full Text] [Related]  

  • 2. The VSR syndrome. Studies of malformation syndromes of man XXXII.
    Herrmann J; Opitz JM
    Birth Defects Orig Artic Ser; 1974; 10(9):227-39. PubMed ID: 4425539
    [No Abstract]   [Full Text] [Related]  

  • 3. Schmid-Fraccaro syndrome ("cat's eye" syndrome).
    Petersen RA
    Arch Ophthalmol; 1973 Oct; 90(4):287-91. PubMed ID: 4746642
    [No Abstract]   [Full Text] [Related]  

  • 4. Microcephaly, distinctive facies, single atrium, postaxial polydactyly, skeletal defects and mental retardation: a new familial faciocardiomelic syndrome?
    García-Ortiz JE; García-Cruz D; Dávalos IP; Nazará Z; García-Cruz MO; Castañeda V; Gutiérrez-Mendivil L; Sánchez-Corona J
    Clin Dysmorphol; 2007 Jan; 16(1):15-20. PubMed ID: 17159509
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Confirmation of the Cohen syndrome.
    Carey JC; Hall BD
    J Pediatr; 1978 Aug; 93(2):239-44. PubMed ID: 671157
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The W syndrome. Studies of malformation syndromes of man XXVIII.
    Pallister PD; Herrmann J; Spranger JW; Gorlin RJ; Langer LO; Opitz JM
    Birth Defects Orig Artic Ser; 1974; 10(7):51-60. PubMed ID: 4425540
    [No Abstract]   [Full Text] [Related]  

  • 7. Syndrome of facial abnormalities, kyphoscoliosis and severe mental retardation.
    Jammes J; Mirhosseini SA; Holmes LB
    Clin Genet; 1973; 4(3):203-9. PubMed ID: 4765203
    [No Abstract]   [Full Text] [Related]  

  • 8. Studies of malformation syndromes of man 33: the FG syndrome. An X-linked recessive syndrome of multiple congenital anomalies and mental retardation.
    Opitz JM; Kaveggia EG
    Z Kinderheilkd; 1974 Apr; 117(1):1-18. PubMed ID: 4365204
    [No Abstract]   [Full Text] [Related]  

  • 9. The Aarskog syndrome.
    Fryns JP; Macken J; Vinken L; Igodt-Ameye L; van den Berghe H
    Hum Genet; 1978 Jun; 42(2):129-35. PubMed ID: 669698
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Letter: Noonan's phenotype in an offspring of an alcoholic mother.
    Hall BD; Orenstein WA
    Lancet; 1974 Apr; 1(7859):680-1. PubMed ID: 4132346
    [No Abstract]   [Full Text] [Related]  

  • 11. The Noonan syndrome--a review of the clinical and genetic features of 27 cases.
    Collins E; Turner G
    J Pediatr; 1973 Dec; 83(6):941-50. PubMed ID: 4148394
    [No Abstract]   [Full Text] [Related]  

  • 12. Sotos syndrome in two brothers.
    Boman H; Nilsson D
    Clin Genet; 1980 Dec; 18(6):421-7. PubMed ID: 7449180
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Johanson-Blizzard syndrome in a large inbred kindred with three involved members.
    Mardini MK; Ghandour M; Sakati NA; Nyhan WL
    Clin Genet; 1978 Nov; 14(5):247-50. PubMed ID: 709902
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Studies of malformation syndromes of man XXXIX: a craniosynostosis-craniofacial dysostosis syndrome with mental retardation and other malformations: "craniofacial dyssynostosis".
    Neuhäuser G; Kaveggia EG; Opitz JM
    Eur J Pediatr; 1976 Aug; 123(1):15-28. PubMed ID: 954768
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Cloverleaf skull syndrome].
    Saji S; Misao A; Hirose T; Funakoshi T; Yamada H
    No To Shinkei; 1977 Apr; 29(4):389-97. PubMed ID: 16629
    [No Abstract]   [Full Text] [Related]  

  • 16. [The Freeman-Sheldon syndrome].
    Grasshoff H; St Braun H; Sakreida M
    Beitr Orthop Traumatol; 1978 May; 25(5):241-7. PubMed ID: 98163
    [No Abstract]   [Full Text] [Related]  

  • 17. See-saw winking in a familial oral-facial-digital syndrome.
    Sugarman GI; Katakia M; Menkes J
    Clin Genet; 1971; 2(4):248-54. PubMed ID: 5004413
    [No Abstract]   [Full Text] [Related]  

  • 18. A case of a girl with a 21 ring chromosome.
    Kucerová M; Polívková Z
    Hum Hered; 1974; 24(1):100-4. PubMed ID: 4136482
    [No Abstract]   [Full Text] [Related]  

  • 19. Autosomal recessive form of whistling face syndrome in sibs.
    Dallapiccola B; Giannotti A; Lembo A; Saguì L
    Am J Med Genet; 1989 Aug; 33(4):542-4. PubMed ID: 2596515
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mandibulofacial dysostosis, microtia, and limb anomalies in a newborn: a new form of acrofacial dysostosis syndrome?
    Zhang Y; Dai Y; Liu Y; Ren J
    Clin Genet; 2010 Dec; 78(6):570-4. PubMed ID: 20412112
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.