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 *

144 related articles for article (PubMed ID: 14120415)

  • 1. ASYMMETRY, SHORT STATURE, AND VARIATIONS IN SEXUAL DEVELOPMENT. A SYNDROME OF CONGENITAL MALFORMATIONS.
    SILVER HK
    Am J Dis Child; 1964 May; 107():495-515. PubMed ID: 14120415
    [No Abstract]   [Full Text] [Related]  

  • 2. Report of a case showing congenital defects, short stature, retarded sexual development and no urinary gonadotropins.
    DORFF GB; APPELMAN DH; LIVESON A
    J Clin Endocrinol Metab; 1947 Dec; 7(12):807-11. PubMed ID: 18901291
    [No Abstract]   [Full Text] [Related]  

  • 3. The Silver syndrome: congenital asymmetry, short stature and variations in sexual development. Roentgen features.
    Moseley JE; Moloshok RE; Freiberger RH
    Am J Roentgenol Radium Ther Nucl Med; 1966 May; 97(1):74-81. PubMed ID: 5938052
    [No Abstract]   [Full Text] [Related]  

  • 4. [CONTRIBUTION TO THE DIAGNOSIS OF GONADAL DYSGENESIS].
    KNAPPE G
    Dtsch Gesundheitsw; 1965 Jan; 20():42-9. PubMed ID: 14265023
    [No Abstract]   [Full Text] [Related]  

  • 5. Congenital asymmetry, short stature, and elevated urinary gonadotropin.
    SILVER HK
    AMA J Dis Child; 1959 Jun; 97(6):768-73. PubMed ID: 13649108
    [No Abstract]   [Full Text] [Related]  

  • 6. STUDIES ON A BOY WITH XXYY CHROMOSOME CONSTITUTION.
    SCHLEGEL RJ; ASPILLAGA MJ; NEU R; GARDNER LI
    Pediatrics; 1965 Jul; 36():113-9. PubMed ID: 14313354
    [No Abstract]   [Full Text] [Related]  

  • 7. BRACHYDACTYLY, PECULIAR FACIES AND MENTAL RETARDATION.
    COFFIN GS
    Am J Dis Child; 1964 Oct; 108():351-9. PubMed ID: 14186654
    [No Abstract]   [Full Text] [Related]  

  • 8. DE LANGE SYNDROME. THE "AMSTERDAM TYPE" OF MENTAL DEFECT WITH CONGENITAL MALFORMATION.
    JERVIS GA; STIMSON CW
    J Pediatr; 1963 Oct; 63():634-45. PubMed ID: 14074421
    [No Abstract]   [Full Text] [Related]  

  • 9. CLUBBING, A REVIEW, WITH EMPHASIS ON HEREDITARY ACROPACHY.
    FISCHER DS; SINGER DH; FELDMAN SM
    Medicine (Baltimore); 1964 Jul; 43():459-79. PubMed ID: 14183519
    [No Abstract]   [Full Text] [Related]  

  • 10. ECTRODACTYLY.
    PILLAY VK
    Singapore Med J; 1965 Jun; 5():110-5. PubMed ID: 14341527
    [No Abstract]   [Full Text] [Related]  

  • 11. GONADAL DYSGENESIS: A REVIEW AND REPORT OF A CASE WITH AN UNUSUAL CHROMOSOMAL ABERRATION.
    CLERKIN EP; MEISNER L
    Lahey Clin Found Bull; 1964; 13():181-9. PubMed ID: 14171917
    [No Abstract]   [Full Text] [Related]  

  • 12. CHROMOSOMAL BREAKAGE IN A RARE AND PROBABLY GENETICALLY DETERMINED SYNDROME OF MAN.
    GERMAN J; ARCHIBALD R; BLOOM D
    Science; 1965 Apr; 148(3669):506-7. PubMed ID: 14263770
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [A STUDY OF CONSTITUTIONAL NANISM. II. RUBINSTEIN AND TAYBI SYNDROME].
    JOB JC; ROSSIER A; DE GRANDPRE YJ
    Ann Pediatr (Paris); 1964 Dec; 11():646-50. PubMed ID: 14255952
    [No Abstract]   [Full Text] [Related]  

  • 14. [THE NATURAL HISTORY OF KLINEFELTER'S DISEASE].
    GILBERT-DREYFUS ; SEBAOUN J; MALINSKY M
    Rev Fr Endocrinol Clin; 1964; 5():465-90. PubMed ID: 14280745
    [No Abstract]   [Full Text] [Related]  

  • 15. [Short stature and genes].
    Koshimizu T; Kato K
    Horumon To Rinsho; 1972 Apr; 20(4):261-9. PubMed ID: 4561537
    [No Abstract]   [Full Text] [Related]  

  • 16. Ring-1 chromosome, microcephalic dwarfism, and acute myeloid leukemia.
    Bobrow M; Emerson PM; Spriggs AI; Ellis HL
    Am J Dis Child; 1973 Aug; 126(2):257-60. PubMed ID: 4125054
    [No Abstract]   [Full Text] [Related]  

  • 17. STUDIES OF A FAMILY WITH THE ORAL-FACIAL-DIGITAL SYNDROME.
    DOEGE TC; THULINE HC; PRIEST JH; NORBY DE; BRYANT JS
    N Engl J Med; 1964 Nov; 271():1073-8. PubMed ID: 14210999
    [No Abstract]   [Full Text] [Related]  

  • 18. [SIMULTANEOUSLY OCCURRING SYN- AND POLYDACTYLY. DATA ON THE HEREDITARY ASPECTS OF THE SYNDROME].
    BOECS G; DEVENYI I
    Orv Hetil; 1964 Apr; 105():747-8. PubMed ID: 14144973
    [No Abstract]   [Full Text] [Related]  

  • 19. [ANTHROPOMETRIC FINDINGS IN GONADAL DYSGENESIS].
    OPPENHEIM M
    Endocrinol Sci Cost; 1964; 28():37-45. PubMed ID: 14196895
    [No Abstract]   [Full Text] [Related]  

  • 20. THE XO SYNDROME. A STUDY OF THE DIFFERENTIATED PHENOTYPE IN 25 PATIENTS.
    LEMLI L; SMITH DW
    J Pediatr; 1963 Oct; 63():577-88. PubMed ID: 14074416
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.