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 *

112 related articles for article (PubMed ID: 5487233)

  • 1. Asymmetrical dwarfism, or Silver's syndrome, in two male siblings.
    Callaghan KA
    Med J Aust; 1970 Oct; 2(17):789-92. PubMed ID: 5487233
    [No Abstract]   [Full Text] [Related]  

  • 2. [Precocious puberty associated with Silver's syndrome].
    Le Goff JY; Cachin O; Rappaport R
    Arch Fr Pediatr; 1977 Nov; 34(9):899-905. PubMed ID: 606190
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Silver's syndrome; a case report and literature review].
    Koike K; Takemoto K; Morishima N; Keibu T
    Nihon Shonika Gakkai Zasshi; 1971; 75(9):816-26. PubMed ID: 5165878
    [No Abstract]   [Full Text] [Related]  

  • 4. Silver's syndrome.
    Vestermark S
    Acta Paediatr Scand; 1970 Jul; 59(4):435-9. PubMed ID: 5447687
    [No Abstract]   [Full Text] [Related]  

  • 5. Orthopaedic considerations of Silver's syndrome.
    Specht EE; Hazelrig PE
    J Bone Joint Surg Am; 1973 Oct; 55(7):1502-10. PubMed ID: 4758720
    [No Abstract]   [Full Text] [Related]  

  • 6. [Silver's syndrome].
    Jelínek J; Havlíková D
    Cesk Pediatr; 1968 Oct; 23(10):913-6. PubMed ID: 5701263
    [No Abstract]   [Full Text] [Related]  

  • 7. The Russell-Silver syndrome: report of three siblings.
    Fuleihan DS; Der Kaloustian VM; Najjar SS
    J Pediatr; 1971 Apr; 78(4):654-7. PubMed ID: 5547822
    [No Abstract]   [Full Text] [Related]  

  • 8. Silver's syndrome: report of a case with chromosomal and dermatoglyphic study.
    Ferrier PE; Ferrier SA
    J Pediatr; 1967 Mar; 70(3):438-40. PubMed ID: 6018399
    [No Abstract]   [Full Text] [Related]  

  • 9. Two examples of Silver's syndrome.
    Sami D
    Clin Pediatr (Phila); 1969 Oct; 8(10):602-3. PubMed ID: 5344426
    [No Abstract]   [Full Text] [Related]  

  • 10. Phenotypic and genetic analysis of the silver-Russell syndrome.
    Escobar V; Gleiser S; Weaver DD
    Clin Genet; 1978 Mar; 13(3):278-88. PubMed ID: 639337
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Silver's syndrome. Silver-Russell's syndrome].
    Vestermark S
    Ugeskr Laeger; 1974 Oct; 136(43):2405. PubMed ID: 4425329
    [No Abstract]   [Full Text] [Related]  

  • 12. [Silver's syndrome. Report of a case].
    Ciorlia VR; Najjar Z; Toledo SP
    AMB Rev Assoc Med Bras; 1975 Nov; 21(11):338-40. PubMed ID: 1082610
    [No Abstract]   [Full Text] [Related]  

  • 13. Elevated serum gonadotrophins in Silver's syndrome.
    Curi JF; Vanucci RC; Grossman H; New M
    Am J Dis Child; 1967 Dec; 114(6):658-61. PubMed ID: 6060029
    [No Abstract]   [Full Text] [Related]  

  • 14. [Diastrophic dwarfism].
    Dorn U; Rosenkranz U; Bösch P
    Z Orthop Ihre Grenzgeb; 1980; 118(3):359-66. PubMed ID: 7415430
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A case of Riley Ruvalcaba syndrome with a novel PTEN mutation accompanied by diffuse testicular microlithiasis and precocious puberty.
    Ozsu E; Sen A; Ceylaner S
    J Pediatr Endocrinol Metab; 2018 Jan; 31(1):95-99. PubMed ID: 29194042
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Low birthweight dwarfism with asymmetry (Silver's syndrome): treatment with human growth hormone.
    Tanner JM; Ham TJ
    Arch Dis Child; 1969 Apr; 44(234):231-43. PubMed ID: 5779433
    [No Abstract]   [Full Text] [Related]  

  • 17. The Russell-Silver syndrome: a nine-year follow-up.
    McDowell RV; Sproles ET
    Am J Dis Child; 1973 Dec; 126(6):794-6. PubMed ID: 4357210
    [No Abstract]   [Full Text] [Related]  

  • 18. Endocrinological anomalies in a patient with 12q14 microdeletion syndrome. Completing phenotype of this exceptional short stature condition.
    Nso-Roca AP; Marco FC; Ricote JM; Ruiz MJ
    J Pediatr Endocrinol Metab; 2014 May; 27(5-6):539-43. PubMed ID: 24468604
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Patient presentation.
    Feingold M; Bull MJ; Darling DB
    Birth Defects Orig Artic Ser; 1974; 10(7):87-91. PubMed ID: 4419732
    [No Abstract]   [Full Text] [Related]  

  • 20. Seckel syndrome: report of three sibships with the type I primordial dwarfism. Possible linkage with HLA locus.
    Stoppoloni G; Stabile M; Rinaldi MM; Prisco F; Rabuano RG; Pace E; Iafusco D; Stoppoloni F; Greco N
    Ann Genet; 1992; 35(4):213-6. PubMed ID: 1296517
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.