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: 1129021)

  • 1. [Central thyroid insufficiency in the 47, XYY syndrome].
    Lévy JM; Stoll C; Krug JP; Kupferberg J
    Pediatrie; 1975 Mar; 30(2):137-43. PubMed ID: 1129021
    [No Abstract]   [Full Text] [Related]  

  • 2. 48,XYYY: a new syndrome?
    Schoepflin GS; Centerwall WR
    J Med Genet; 1972 Sep; 9(3):356-60. PubMed ID: 4116771
    [No Abstract]   [Full Text] [Related]  

  • 3. 49, XXXXY syndrome in a 1 year-old infant.
    Molska I; Lech H; Wiśniewski L
    Klin Padiatr; 1977 Nov; 189(6):477-81. PubMed ID: 563945
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Penta X (49,XXXXX) chromosome constitution: a case report.
    Yamada Y; Neriishi S
    Jinrui Idengaku Zasshi; 1971 Aug; 16(1):15-21. PubMed ID: 5166615
    [No Abstract]   [Full Text] [Related]  

  • 5. [The XYY status in children].
    Keutel J; Dauner I
    Z Kinderheilkd; 1969; 106(4):314-32. PubMed ID: 4980303
    [No Abstract]   [Full Text] [Related]  

  • 6. [Case of chromosome X pentasomy].
    Sito A; Krzyzanowska J; Hofman H; Witkowska J; Sioch R; Mroczek-Orłow T
    Pediatr Pol; 1980 Jan; 55(1):77-80. PubMed ID: 7367071
    [No Abstract]   [Full Text] [Related]  

  • 7. [Growth disturbances in children and therapeutic possibilities].
    Trygstad O
    Tidsskr Nor Laegeforen; 1973 Mar; 93(8):520-3. PubMed ID: 4697593
    [No Abstract]   [Full Text] [Related]  

  • 8. Trisomy 1q43 syndrome: a consistent phenotype with macrocephaly, characteristic face, developmental delay and cardiac anomalies.
    Morava E; Jackson KE; Tsien F; Marble MR
    Genet Couns; 2004; 15(4):449-53. PubMed ID: 15658621
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [49, XXXXX syndrome in a 5-year-old girl].
    Larget-Piet L; Rivron J; Baillif P; Dugay J; Emerit I; Larget-Piet A; Berthelot J
    Ann Genet; 1972 Jun; 15(2):115-9. PubMed ID: 4537723
    [No Abstract]   [Full Text] [Related]  

  • 10. [XXX syndrome. Apropos of a case].
    Choisel G; Parent JP; Biéder J
    Ann Med Psychol (Paris); 1970 May; 128(5):765-71. PubMed ID: 5452654
    [No Abstract]   [Full Text] [Related]  

  • 11. [XXXXY syndrome].
    Toudic L; L'Henoret G; Rivière D; L'Hour M; Castel Y
    Arch Fr Pediatr; 1982 Apr; 39(4):247-9. PubMed ID: 7125819
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The leopard (multiple lentigines) syndrome revisited.
    Gorlin RJ; Anderson RC; Moller JH
    Laryngoscope; 1971 Oct; 81(10):1674-81. PubMed ID: 4398858
    [No Abstract]   [Full Text] [Related]  

  • 13. [2 cases of triplo-X with epileptic seizure].
    Takei H; Asaka A; Kurihara T
    No To Shinkei; 1969 May; 21(5):523-32. PubMed ID: 5394316
    [No Abstract]   [Full Text] [Related]  

  • 14. [XXXXY phenotype: synthetic and analytic study of 3 personal cases and 67 other cases in the literature].
    Tumba A
    J Genet Hum; 1972 Mar; 20(1):9-48. PubMed ID: 4643878
    [No Abstract]   [Full Text] [Related]  

  • 15. Congenital heart disease in 49, XXXXY syndrome.
    Karsh RB
    Pediatrics; 1975 Sep; 56(3):462-4. PubMed ID: 1161403
    [No Abstract]   [Full Text] [Related]  

  • 16. [Contribution to the "XYY syndrome"].
    Zernahle K; Polster H
    Kinderarztl Prax; 1969 Jul; 37(7):324-34. PubMed ID: 5355990
    [No Abstract]   [Full Text] [Related]  

  • 17. The syndrome of the metacentric microchromosome.
    Abbo G; Zellweger H
    Helv Paediatr Acta; 1970 Jan; 25(1):83-94. PubMed ID: 4392428
    [No Abstract]   [Full Text] [Related]  

  • 18. ["Superfemale syndrome" in a 12-year-old girl (XXXX sex chromosome arrangement) associated with a combination of congenital abnormalities].
    Halikowski B; Kleczkowska A; Gościńska Z; Knaus A
    Pediatr Pol; 1969 Sep; 44(9):1147-54. PubMed ID: 5364501
    [No Abstract]   [Full Text] [Related]  

  • 19. The interplay of biological and environmental factors in a preschool-age patient with Klinefelter's syndrome. Case report.
    Campbell M; Breuer H; Wolman SR
    Pediatrics; 1973 Jul; 52(1):29-37. PubMed ID: 4125079
    [No Abstract]   [Full Text] [Related]  

  • 20. Mental defects and disorders of behaviour in children. Chromosomal and dermatoglyphic studies in mental defectives, with special reference to Down's syndrome.
    Fukuyama Y; Matsui I; Higurashi M
    Proc Aust Assoc Neurol; 1968; 5(1):129-37. PubMed ID: 4237078
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.